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| Product | Description | |
|---|---|---|
| Dodecyl trimethyl ammonium sulfate | Dodecyl trimethyl ammonium sulfate. Product ID: ACMA00004124. Molecular formula: C15H35NO4S. Mole weight: 325.51. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Dodemorph acetate | Dodemorph acetate. Group: Biochemicals. Grades: Highly Purified. CAS No. 1593-77-7. Pack Sizes: 100mg, 250mg, 500mg. US Biological Life Sciences. |  Worldwide |
| Dodine | Used as agricultural fungicide. Group: Biochemicals. Alternative Names: N-Dodecylguanidine Acetate; AC 5223; Aadodin; Carpene; Comet; Cyprex; Cyprex 65W; Dodecylguanidinium Acetate; Dodex; Dodex (pesticide); Dodin; Dodine; Dodine 400; Doguadine; Karpen; Laurylguanidine Acetate; Melprex; Melprex 65; Melprex 65W; Melprex Liquid Dodine; Radspor; Syllit; Syllit 65. Grades: Highly Purified. CAS No. 2439-10-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| DODMA | DODMA is a cationic lipid containing the unsaturated oleic acid. It can be used in formulation of liposomes for drug delivery system. Synonyms: 1-Propanamine, N,N-dimethyl-2,3-bis[(9Z)-9-octadecenyloxy]-; 1,2-Dioleyloxy-3-dimethylamino-propane; ACMC-20m6xx; ACMC-20m7p2; 1-Propanamine, N,N-dimethyl-2,3-bis[(9Z)-9-octadecenyloxy]-, (2S)-; (2,3-bis-octadec-9-enyloxypropyl)-dimethylamine; 1,2-dioleyloxy-N,N-dimethylaminopropane; N-[2,3-Di(oleyloxy)propyl]-N,N-dimethylamine; 2,3-Dioleyloxy-1-(dimethylamino)propane; 2-amino-2,3-dimethyloleanol; 2,3-Dioleyloxy-1-(dimethylamino)propane. Grade: >98% by HPLC. CAS No. 104162-47-2. Molecular formula: C41H81NO2. Mole weight: 620.08. |  |
| DODMA | DODMA is a cationic lipid that can be used to prepare lipid nanoparticles. DODMA can be used for drug delivery[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 104162-47-2. Pack Sizes: 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-112755. |  |
| Dodovislactone B | Dodovislactone B is extracted from the aerial parts of Dodonaea viscosa. Synonyms: Dodovislactone B; 1616683-55-6; (4Ar,5S,6R,8aR)-5-[2-(2-methoxy-5-oxo-2H-furan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid. CAS No. 1616683-55-6. Molecular formula: C21H30O5. Mole weight: 362.46. | |
| Dodovisone B | Dodovisone B is extracted from the aerial parts of Dodonaea viscosa. Synonyms: Dodovisone B; 1616683-51-2; 5,7-dihydroxy-2-[3-hydroxy-8-(4-hydroxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3,6-dimethoxychromen-4-oneB0005-2677042-[3,4-dihydro-3-hydroxy-8-(4-hydroxy-3-methylbutyl)-2,2-dimethyl-2h-1-benzopyran-6-yl]-5,7-dihydroxy-3,6-dimethoxy-4h-1-benzopyran-4-one. Grade: 90%. CAS No. 1616683-51-2. Molecular formula: C27H32O9. Mole weight: 500.54. | |
| Dofequidar | Dofequidar, also known as MS-209, is a quinolone-derived sphingomyelin synthase inhibitor that blocks P-glycoprotein and multidrug resistance-associated protein-1, is under development by Schering for the potential treatment of multidrug resistant tumors. Dofequidar was found to sensitizes cancer stem-like side population cells to chemotherapeutic drugs by inhibiting ABCG2/BCRP-mediated drug export. Uses: Antineoplastic agents. Synonyms: Dofequidar. CAS No. 129716-58-1. Molecular formula: C30H31N3O3. Mole weight: 481.596. | |
| Dofequidar fumarate | Dofequidar fumarate, a quinoline derivative, is a multidrug resistance (MDR)-reversing quinoline derivative by inhibiting ABCB1/P-gp, ABCC1/MDR-associated protein 1, or both. It has potential to treat advanced and recurrent breast cancer and non-small lun. Synonyms: MS-209; MS 209; MS209. CAS No. 153653-30-6. Molecular formula: C34H35N3O7. Mole weight: 597.66. | |
| Dofetilide | Dofetilide is a selective potassium channel ((hERG)) blocker, used as a Class III antiarrhythmic drug. Synonyms: UK 68798; UK 68798; UK 68798; Dofetilide; Dofetilidum; Tikosyn. Grade: >98%. CAS No. 115256-11-6. Molecular formula: C19H27N3O5S2. Mole weight: 441.56. | |
| Dofetilide | Dofetilide (UK 68789), as a class III antiarrhythmic agent, is an orally active, potent and specific IKr blocker. Dofetilide can be used for the research of cardiovascular disease[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UK 68789. CAS No. 115256-11-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0232. | |
| Dofetilide-[d4] | Dofetilide-[d4] is a labelled Dofetilide. Dofetilide is a medication used for the treatment of arythmia. Synonyms: Dofetilide D4; N-[4-[2-[Methyl[2-[4-[(methylsulfonyl)amino]phenoxy]ethyl]amino]ethyl]phenyl]-methanesulfonamide-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 1189700-56-8. Molecular formula: C19H23D4N3O5S2. Mole weight: 445.59. | |
| Dofetilide Impurity 1 | Dofetilide Impurity 1. Uses: For analytical and research use. Molecular formula: C18H24N4O6S2. Mole weight: 456.53. Catalog: APB12187. |  |
| DOI hydrochloride | DOI hydrochloride is a serotonin 5-HT2A/2C receptor agonist with Ki values of 0.7 nM, 2.4 nM and 20 nM for h5-HT2A, h5-HT2C and h5-HT2B receptors, respectively. DOI hydrochloride can across the blood-brain barrier. DOI hydrochloride increases head twitches in mice[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 42203-78-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103124. | |
| Dolabellanin-B2 | Dolabellanin-B2 has antibacterial activity against Gram-negative bacteria E.coli JM109 and DH5-alpha, H.influenza IID 983, and V.vulnificus RIMD 2219009. Dolabellanin-B2 has antibacterial activity against Gram-positive bacteria S.aureus IID 1677, B.subtilis RIMD 0225014 and L.monocytogenes VIU206. It also possesses antifungal activity against S.cerevisiae A581A, S.pombe IFO 1628, C.albicans and TIMM-1623, and C.tropicalis TIMM-0313. | |
| Dolasetron | Bridged pseudopelletierine derivative; specific serotonin (5HT3) receptor antagonist. Antiemetic. Group: Biochemicals. Alternative Names: Octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl Ester. Grades: Highly Purified. CAS No. 115956-12-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Dolasetron | Dolasetron (MDL-73147) is a serotonin 5-HT3 receptor antagonist. Dolasetron acts as an antiemetics agent and can be used for the research of chemotherapy-induced nausea and vomiting in cancer[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MDL-73147. CAS No. 115956-12-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B0750. | |
| Dolasetron | Dolasetron, a pseudopelletierine derivative, is a 5-HT3 receptor antagonist that could be used to relieve the nausea and vomiting caused by chemotherapy. Synonyms: 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, stereoisomer; 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, (2α,6α,8α,9aβ)-; Anemet; MDL 73147. Grade: 95%. CAS No. 115956-12-2. Molecular formula: C19H20N2O3. Mole weight: 324.37. | |
| Dolasetron Impurity 3 | Dolasetron Impurity 3. Uses: For analytical and research use. Alternative Names: 7-acetyl-9-azabicyclo[3.3.1]nonan-3-yl 1H-indole-3-carboxylate. Molecular formula: C19H22N2O3. Mole weight: 326.39. Catalog: APB05449. | |
| Dolasetron Impurity 4 | Dolasetron Impurity 4. Uses: For analytical and research use. Alternative Names: (5s,6R,8s,9aS)-8-hydroxyhexahydro-1H-2,6-methanoquinolizin-3(2H)-one. Molecular formula: C10H15NO2. Mole weight: 181.23. Catalog: APB05448. | |
| Dolasetron Impurity 5 | Dolasetron Impurity 5. Uses: For analytical and research use. Alternative Names: ethyl 9-(2-ethoxy-2-oxoethyl)-7-oxo-9-azabicyclo[3.3.1]nonane-3-carboxylate. CAS No. 115956-03-1. Molecular formula: C15H23NO5. Mole weight: 297.35. Catalog: APB115956031. | |
| Dolasetron mesylate | Dolasetron mesylate. Group: Biochemicals. Grades: Highly Purified. CAS No. 115956-13-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C20H24N2O6S·H2O. US Biological Life Sciences. | Worldwide |
| Dolasetron mesylate | The mesylate salt form of Dolasetron which is a pseudopelletierine derivative and could be used to relieve the nausea and vomiting caused by chemotherapy for behaving as a 5-HT3 receptor antagonist. Synonyms: Dolasetron methanesulfonate; Dolasetron mesilate. Grade: 98%. CAS No. 115956-13-3. Molecular formula: C19H20N2O3.CH4O3S. Mole weight: 420.48. | |
| Dolastatin 10 | Dolastatin 10 (DLS 10) is a potent antimitotic peptide that inhibits tubulin polymerization. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DLS 10; NSC 376128. CAS No. 110417-88-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15580. | |
| Dolastatin 10 | Dolastatin 10 is a potent antimitotic peptide from a marine animal, strongly inhibiting microtubule assembly. Uses: Adcs cytotoxin. Synonyms: DLS 10; NSC 376128; Dolastatin-10; DLS-10; DLS10; NSC376128; NSC-376128; L-Valinamide, N,N-dimethyl-L-valyl-N-[2-methoxy-4-[2-[1-methoxy-2-methyl-3-oxo-3-[[2-phenyl-1-(2-thiazolyl)ethyl]amino]propyl]-1-pyrrolidinyl]-1-(1-methylpropyl)-4-oxobutyl]-N-methyl-,[2S-[1[1R*(R*),2S*],2R*[1S*,2S*,3(R*)]]]-. Grade: >98%. CAS No. 110417-88-4. Molecular formula: C42H68N6O6S. Mole weight: 785.09. | |
| Dolastatin 10 trifluoroacetate | Dolastatin 10 trifluoroacetate inhibits tubulin polymerization and induces tubulin aggregation in vitro. Synonyms: Dolastatin 10 trifluoroacetate; 2342568-65-2; EX-A8176; AKOS027470141; AKOS040745145; PD080063; Dolastatin 10 trifluoroacetate (110417-88-4 free base); (2S)-2-[[(2S)-2-(dimethylamino)-3-methylbutanoyl]amino]-N-[(3R,4S,5S)-3-methoxy-1-[(2S)-2-[(1R,2R)-1-methoxy-2-methyl-3-oxo-3-[[(1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethyl]amino]propyl]pyrrolidin-1-yl]-5-methyl-1-oxoheptan-4-yl]-N,3-dimethylbutanamide; 2,2,2-trifluoroacetic acid; N,N-Dimethyl-L-valyl-N-[(1S,2R)-2-methoxy-4-[(2S)-2-[(1R,2R)-1-methoxy-2-methyl-3-oxo-3-[[(1S)-2-phenyl-1-(2-thiazol)ethyl]amino]propyl]-1-pyrrolidinyl]-1-[(1S)-1-methylpropyl]-4-oxobutyl]-N-methyl--valinamide trifluoroacetate. CAS No. 2342568-65-2. Molecular formula: C42H68N6O6S.CF3CO2H. Mole weight: 899.11. | |
| Dolastatin 15 | Dolastatin 15 (DLS 15), a depsipeptide derived from Dolabella auricularia, is a potent antimitotic agent structurally related to the antitubulin agent Dolastatin 10. Dolastatin 15 induces cell cycle arrest and apoptosis in multiple myeloma cells. Dolastatin 15 can be used as an ADC cytotoxin. Synonyms: DLS 15; (S)-1-((S)-2-benzyl-3-methoxy-5-oxo-2,5-dihydro-1H-pyrrol-1-yl)-3-methyl-1-oxobutan-2-yl N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-prolyl-L-prolinate; L-Proline, N,N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-prolyl-, (1S)-1-[[(2S)-2,5-dihydro-3-methoxy-5-oxo-2-(phenylmethyl)-1H-pyrrol-1-yl]carbonyl]-2-methylpropyl ester. Grade: ≥98%. CAS No. 123884-00-4. Molecular formula: C45H68N6O9. Mole weight: 837.06. | |
| Dolasteron | Dolasteron. Alternative Names: DOLASETRON;(+-)-2-(p-(2-thenoyl)phenyl)propionicacid;alpha-methyl-4-(2-thienylcarbonyl)-benzeneaceticaci;alpha-methyl-4-(2-thienylcarbonyl)benzeneaceticacid;maldocil;p-(2-thenoyl)-hydratropicaci;p-(2-thenoyl)hydratropicacid;r25061. CAS No. 40828-46-4. Purity: 98%+. Product ID: ACM40828464. Molecular formula: C14H12O3S. Mole weight: 260.30828. IUPAC Name: 2-[4-(thiophene-2-carbonyl)phenyl]propanoicacid. Canonical SMILES: CC(C1=CC=C(C=C1)C(=O)C2=CC=CS2)C(=O)O. ECNumber: 255-096-9. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Dolichol-18 | Dolichol-18. Group: Biochemicals. Grades: Highly Purified. CAS No. 153857-77-3. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C65H108O. US Biological Life Sciences. | Worldwide |
| Dolichol-20 | Dolichol-20. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Dolichol-22 | Dolichol-22. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| dolichol kinase | This enzyme belongs to the family of transferases, to be specific, those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is CTP:dolichol O-phosphotransferase. This enzyme is also called dolichol phosphokinase. This enzyme participates in N-glycan biosynthesis. In humans dolichol kinase is encoded by the DOLK gene. Group: Enzymes. Synonyms: dolichol phosphokinase. Enzyme Commission Number: EC 2.7.1.108. CAS No. 71768-07-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2954; dolichol kinase; EC 2.7.1.108; 71768-07-5; dolichol phosphokinase. Cat No: EXWM-2954. |  |
| dolichol O-acyltransferase | Other acyl-CoAs can also act, but more slowly. α-Saturated dolichols are acylated more rapidly than the α-unsaturated analogues. Group: Enzymes. Synonyms: acyl-CoA:dolichol acyltransferase. Enzyme Commission Number: EC 2.3.1.123. CAS No. 111839-04-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2061; dolichol O-acyltransferase; EC 2.3.1.123; 111839-04-4; acyl-CoA:dolichol acyltransferase. Cat No: EXWM-2061. | |
| Dolichorrhizin | Dolichorrhizin. Synonyms: 15α-Acetyloxyhopan-22-ol; Hopane-15α,22-diol 15-acetate; Acetic acid (3S,3aS,5S,5aR,5bR,11aS,13aR,13bS)-3-(1-hydroxy-1-methyl-ethyl)-5a,5b,8,8,11a,13b-hexamethyl-icosahydro-cyclopenta[a]chrysen-5-yl ester. CAS No. 3607-97-4. Molecular formula: C32H54O3. Mole weight: 486.77. | |
| dolichyldiphosphatase | This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. This enzyme participates in n-glycan biosynthesis. Group: Enzymes. Synonyms: dolichol diphosphatase; dolichyl pyrophosphatase; dolichyl pyrophosphate phosphatase; dolichyl diphosphate phosphohydrolase; Dol-P-P phosphohydrolase. Enzyme Commission Number: EC 3.6.1.43. CAS No. 73361-26-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4620; dolichyldiphosphatase; EC 3.6.1.43; 73361-26-9; dolichol diphosphatase; dolichyl pyrophosphatase; dolichyl pyrophosphate phosphatase; dolichyl diphosphate phosphohydrolase; Dol-P-P phosphohydrolase. Cat No: EXWM-4620. | |
| dolichyl-diphosphate-polyphosphate phosphotransferase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with a phosphate group as acceptor. Group: Enzymes. Synonyms: dolichylpyrophosphate:polyphosphate phosphotransferase. Enzyme Commission Number: EC 2.7.4.20. CAS No. 94949-27-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3202; dolichyl-diphosphate-polyphosphate phosphotransferase; EC 2.7.4.20; 94949-27-6; dolichylpyrophosphate:polyphosphate phosphotransferase. Cat No: EXWM-3202. | |
| dolichyl-diphosphooligosaccharide-protein glycotransferase | Occurs in eukaryotes that form a glycoprotein by the transfer of a glucosyl-mannosyl-glucosamine polysaccharide to the side-chain of an L-asparagine residue in the sequence -Asn-Xaa-Ser- or -Asn-Xaa-Thr- (Xaa not Pro) in nascent polypeptide chains. The basic oligosaccharide is the tetradecasaccharide Glc3Man9GlcNAc2 (for diagram click here). However, smaller oligosaccharides derived from it and oligosaccharides with additional monosaccharide units attached may be involved. See ref for a review of N-glycoproteins in eukaryotes. Man3GlcNAc2 seems to be common for all of the oligosaccharides involved with the terminal N-acetylglucosamine linked to the protein L-aspa. oligopolysaccharidotransferase; STT3. Enzyme Commission Number: EC 2.4.99.18. CAS No. 75302-32-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2702; dolichyl-diphosphooligosaccharide-protein glycotransferase; EC 2.4.99.18; 75302-32-8; dolichyldiphosphooligosaccharide-protein glycosyltransferase; asparagine N-glycosyltransferase; dolichyldiphosphooligosaccharide-protein oligosaccharyltransferase; dolichyl pyrophosphodiacetyl chitobiose-protein glycosyltransferase; oligomannosyltransferase; oligosaccharide transferase; dolichyldiphosphoryloligosaccharide-protein oligosaccharyl. | |
| dolichyl N-acetyl-α-D-glucosaminyl phosphate 3-β-D-2,3-diacetamido-2,3-dideoxy-β-D-glucuronosyltransferase | The enzyme, characterized from the methanogenic archaeon Methanococcus voltae, participates in the N-glycosylation of proteins. Dolichol used by archaea is different from that used by eukaryotes. It is much shorter (C55-C60), it is α,ω-saturated and it may have additional unsaturated positions in the chain. Group: Enzymes. Synonyms: AglC; UDP-Glc-2,3-diNAcA glycosyltransferase. Enzyme Commission Number: EC 2.4.1.335. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2573; dolichyl N-acetyl-α-D-glucosaminyl phosphate 3-β-D-2,3-diacetamido-2,3-dideoxy-β-D-glucuronosyltransferase; EC 2.4.1.335; AglC; UDP-Glc-2,3-diNAcA glycosyltransferase. Cat No: EXWM-2573. | |
| dolichyl N-acetyl-α-D-glucosaminyl phosphate 3-β-D-2,3-diacetamido-2,3-dideoxy-β-D-glucuronosyltransferase | The enzyme, characterized from the methanogenic archaeon Methanococcus voltae, participates in the N-glycosylation of proteins. Dolichol used by archaea is different from that used by eukaryotes. It is much shorter (C55-C60), it is α,ω-saturated and it may have additional unsaturated positions in the chain. | |
| dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase | The successive addition of three glucose residues by EC 2.4.1.267 (dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase), EC 2.4.1.265 and EC 2.4.1.256 (dolichyl-P-Glc:Glc2Man9GlcNAc2-PP-dolichol α-1,2-glucosyltransferase) represents the final stage of the lipid-linked oligosaccharide assembly. | |
| dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase | The successive addition of three glucose residues by EC 2.4.1.267 (dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase), EC 2.4.1.265 and EC 2.4.1.256 (dolichyl-P-Glc:Glc2Man9GlcNAc2-PP-dolichol α-1,2-glucosyltransferase) represents the final stage of the lipid-linked oligosaccharide assembly. Group: Enzymes. Synonyms: ALG8; Dol-P-Glc:Glc1Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase; dolichyl β-D-glucosyl phosphate:D-Glc-α-(1?3)-D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?6)]-D-Man-α-(1?6)]-D-M. Enzyme Commission Number: EC 2.4.1.265. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2496; dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase; EC 2.4.1.265; ALG8; Dol-P-Glc:Glc1Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase; dolichyl β-D-glucosyl phosphate:D-Glc-α-(1?3)-D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?6)]-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-1,3-glucosyltransferase. Cat No: EXWM-2496. | |
| dolichyl-P-Glc:Glc2Man9GlcNAc2-PP-dolichol α-1,2-glucosyltransferase | This eukaryotic enzyme performs the final step in the synthesis of the lipid-linked oligosaccharide, attaching D-glucose in an α-1,2-linkage to the outermost D-glucose in the long branch. The lipid-linked oligosaccharide is involved in N-linked protein glycosylation of selected asparagine residues of nascent polypeptide chains in eukaryotic cells. Group: Enzymes. Synonyms: ALG10; Dol-P-Glc:Glc2Man9GlcNAc2-PP-Dol α-1,2-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.256. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2486; dolichyl-P-Glc:Glc2Man9GlcNAc2-PP-dolichol α-1,2-glucosyltransferase; EC 2.4.1.256; ALG10; Dol-P-Glc:Glc2Man9GlcNAc2-PP-Dol α-1,2-glucosyltransferase. Cat No: EXWM-2486. | |
| dolichyl-P-Glc:Glc2Man9GlcNAc2-PP-dolichol α-1,2-glucosyltransferase | This eukaryotic enzyme performs the final step in the synthesis of the lipid-linked oligosaccharide, attaching D-glucose in an α-1,2-linkage to the outermost D-glucose in the long branch. The lipid-linked oligosaccharide is involved in N-linked protein glycosylation of selected asparagine residues of nascent polypeptide chains in eukaryotic cells. | |
| dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase | The successive addition of three glucose residues by EC 2.4.1.267, EC 2.4.1.265 (Dol-P-Glc:Glc1Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase) and EC 2.4.1.256 (Dol-P-Glc:Glc2Man9GlcNAc2-PP-Dol α-1,2-glucosyltransferase) represents the final stage of the lipid-linked oligosaccharide assembly. | |
| dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase | The successive addition of three glucose residues by EC 2.4.1.267, EC 2.4.1.265 (Dol-P-Glc:Glc1Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase) and EC 2.4.1.256 (Dol-P-Glc:Glc2Man9GlcNAc2-PP-Dol α-1,2-glucosyltransferase) represents the final stage of the lipid-linked oligosaccharide assembly. Group: Enzymes. Synonyms: ALG6; Dol-P-Glc:Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase; dolichyl β-D-glucosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?6)]-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol &alpha. Enzyme Commission Number: EC 2.4.1.267. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2498; dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol α-1,3-glucosyltransferase; EC 2.4.1.267; ALG6; Dol-P-Glc:Man9GlcNAc2-PP-Dol α-1,3-glucosyltransferase; dolichyl β-D-glucosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?6)]-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-1,3-glucosyltransferase. Cat No: EXWM-2498. | |
| dolichyl-phosphatase | This enzyme belongs to the family of hydrolases, to be specific, those acting on phosphoric monoester bonds. The systematic name of this enzyme class is dolichyl-phosphate phosphohydrolase. Other names in common use include dolichol phosphate phosphatase, dolichol phosphatase, dolichol monophosphatase, dolichyl monophosphate phosphatase, dolichyl phosphate phosphatase, polyisoprenyl phosphate phosphatase, polyprenylphosphate phosphatase, and Dol-P phosphatase. This enzyme participates in n-glycan biosynthesis. Group: Enzymes. Synonyms: dolichol phosphate phosphatase; dolichol phosphatase; dolichol monophosphatase; dolichyl monophosphate phosphatase; dolichyl phosphate phosphatase; polyisoprenyl phosphate phosphatase; polyprenylphosphate phosphatase; Dol-P phosphatase. Enzyme Commission Number: EC 3.1.3.51. CAS No. 72994-50-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3656; dolichyl-phosphatase; EC 3.1.3.51; 72994-50-4; dolichol phosphate phosphatase; dolichol phosphatase; dolichol monophosphatase; dolichyl monophosphate phosphatase; dolichyl phosphate phosphatase; polyisoprenyl phosphate phosphatase; polyprenylphosphate phosphatase; Dol-P phosphatase. Cat No: EXWM-3656. | |
| dolichyl-phosphate β-D-mannosyltransferase | Acts only on long-chain polyprenyl phosphates and α-dihydropolyprenyl phosphates that are larger than C35. Group: Enzymes. Synonyms: GDP-Man:DolP mannosyltransferase; dolichyl mannosyl phosphate synthase; dolichyl-phospho-mannose synthase; GDP-mannose:dolichyl-phosphate mannosyltransferase; guanosine diphosphomannose-dolichol phosphate mannosyltransferase; dolichol phosphate mannose synthase; dolichyl phosphate mannosyltransferase; dolichyl-phosphate mannose synthase; GDP-mannose-dolichol phosphate mannosyltransferase; GDP-mannose. Enzyme Commission Number: EC 2.4.1.83. CAS No. 62213-44-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2624; dolichyl-phosphate β-D-mannosyltransferase; EC 2.4.1.83; 62213-44-9; GDP-Man:DolP mannosyltransferase; dolichyl mannosyl phosphate synthase; dolichyl-phospho-mannose synthase; GDP-mannose:dolichyl-phosphate mannosyltransferase; guanosine diphosphomannose-dolichol phosphate mannosyltransferase; dolichol phosphate mannose synthase; dolichyl phosphate mannosyltransferase; dolichyl-phosphate mannose synthase; GDP-mannose-dolichol phosphate mannosyltransferase; GDP-mannose-dolichylmonophosphate mannosyltransferase; mannosylphosphodolichol synthase; mannosylphosphoryldolichol synthase. Cat No: EXWM-2624. | |
| dolichyl-phosphate β-glucosyltransferase | Solanesyl phosphate and ficaprenyl phosphate can act as acceptors, but more slowly. Group: Enzymes. Synonyms: polyprenyl phosphate:UDP-D-glucose glucosyltransferase; UDP-glucose dolichyl-phosphate glucosyltransferase; uridine diphosphoglucose-dolichol glucosyltransferase; UDP-glucose:dolichol phosphate glucosyltransferase; UDP-glucose:dolicholphosphoryl glucosyltransferase; UDP-glucose:dolichyl monophosphate glucosyltransferase; UDP-glucose:dolichyl phosphate glucosyltransferase. Enzyme Commission Number: EC 2.4.1.117. CAS No. 71061-42-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2343; dolichyl-phosphate β-glucosyltransferase; EC 2.4.1.117; 71061-42-2; polyprenyl phosphate:UDP-D-glucose glucosyltransferase; UDP-glucose dolichyl-phosphate glucosyltransferase; uridine diphosphoglucose-dolichol glucosyltransferase; UDP-glucose:dolichol phosphate glucosyltransferase; UDP-glucose:dolicholphosphoryl glucosyltransferase; UDP-glucose:dolichyl monophosphate glucosyltransferase; UDP-glucose:dolichyl phosphate glucosyltransferase. Cat No: EXWM-2343. | |
| dolichyl-phosphate D-xylosyltransferase | This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. The systematic name of this enzyme class is UDP-D-xylose:dolichyl-phosphate D-xylosyltransferase. Group: Enzymes. Enzyme Commission Number: EC 2.4.2.32. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2660; dolichyl-phosphate D-xylosyltransferase; EC 2.4.2.32. Cat No: EXWM-2660. | |
| dolichylphosphate-glucose phosphodiesterase | This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric diester bonds. This enzyme participates in n-glycan biosynthesis. Group: Enzymes. Synonyms: dolichol phosphoglucose phosphodiesterase; Dol-P-Glc phosphodiesterase. Enzyme Commission Number: EC 3.1.4.48. CAS No. 89287-42-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3731; dolichylphosphate-glucose phosphodiesterase; EC 3.1.4.48; 89287-42-3; dolichol phosphoglucose phosphodiesterase; Dol-P-Glc phosphodiesterase. Cat No: EXWM-3731. | |
| dolichylphosphate-mannose phosphodiesterase | This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric diester bonds. Group: Enzymes. Synonyms: mannosylphosphodolichol phosphodiesterase. Enzyme Commission Number: EC 3.1.4.49. CAS No. 111839-07-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3732; dolichylphosphate-mannose phosphodiesterase; EC 3.1.4.49; 111839-07-7; mannosylphosphodolichol phosphodiesterase. Cat No: EXWM-3732. | |
| dolichyl-phosphate-mannose-protein mannosyltransferase | The enzyme transfers mannosyl residues to the hydroxy group of serine or threonine residues, producing cell-wall mannoproteins. It acts only on long-chain α-dihydropolyprenyl derivatives, larger than C35. Group: Enzymes. Synonyms: dolichol phosphomannose-protein mannosyltransferase; protein O-D-mannosyltransferase; dolichyl-phosphate-D-mannose:protein O-D-mannosyltransferase; dolichyl-phosphate-mannose-protein mannosyltransferase. Enzyme Commission Number: EC 2.4.1.109. CAS No. 74315-99-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2335; dolichyl-phosphate-mannose-protein mannosyltransferase; EC 2.4.1.109; 74315-99-4; dolichol phosphomannose-protein mannosyltransferase; protein O-D-mannosyltransferase; dolichyl-phosphate-D-mannose:protein O-D-mannosyltransferase; dolichyl-phosphate-mannose-protein mannosyltransferase. Cat No: EXWM-2335. | |
| dolichyl-phosphooligosaccharide-protein glycotransferase | The enzyme, characterized from the archaea Methanococcus voltae and Haloferax volcanii, transfers a glycan component from dolichyl phosphooligosaccharide to external proteins. It is different from EC 2.4.99.18, dolichyl-diphosphooligosaccharide-protein glycotransferase, which uses dolichyl diphosphate as carrier compound in bacteria and eukaryotes. The enzyme participates in the N-glycosylation of proteins in some archaea. It requires Mn2+. Dolichol used by archaea is different from that used by eukaryotes. It is much shorter (C55-C60), it is α,ω-saturated and it may have additional unsaturated positions in the chain. Group: Enzymes. Synonyms: AglB; archaeal oligosaccharyl transferase; dolichyl-monophosphooligosaccharide-protein glycotransferase. Enzyme Commission Number: EC 2.4.99.21. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2706; dolichyl-phosphooligosaccharide-protein glycotransferase; EC 2.4.99.21; AglB; archaeal oligosaccharyl transferase; dolichyl-monophosphooligosaccharide-protein glycotransferase. Cat No: EXWM-2706. | |
| dolichyl-P-Man:Man5GlcNAc2-PP-dolichol α-1,3-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-dolichol to Man9Glc-NAc2-PP-dolichol on the lumenal side use dolichyl β-D-mannosyl phosphate. The first step of this assembly pathway on the luminal side of the endoplasmic reticulum is catalysed by ALG3. Group: Enzymes. Synonyms: Man5GlcNAc2-PP-Dol mannosyltr. Enzyme Commission Number: EC 2.4.1.258. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2488; dolichyl-P-Man:Man5GlcNAc2-PP-dolichol α-1,3-mannosyltransferase; EC 2.4.1.258; Man5GlcNAc2-PP-Dol mannosyltransferase; ALG3; dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase; Not56-like protein; Alg3 α-1,3-mannosyl transferase; Dol-P-Man:Man5GlcNAc2-PP-Dol α-1,3-mannosyltransferase; dolichyl β-D-mannosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-1,3-mannosyltransferase. Cat No: EXWM-2488. | |
| dolichyl-P-Man:Man5GlcNAc2-PP-dolichol α-1,3-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-dolichol to Man9Glc-NAc2-PP-dolichol on the lumenal side use dolichyl β-D-mannosyl phosphate. The first step of this assembly pathway on the luminal side of the endoplasmic reticulum is catalysed by ALG3. | |
| dolichyl-P-Man:Man6GlcNAc2-PP-dolichol α-1,2-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. ALG9 mannosyltransferase catalyses the addition of two different α-1,2-mannose residues - the addition of α-1,2-mannose to Man6GlcNAc2-PP-Dol (EC 2.4.1.259) and the addition of α-1,2-mannose to Man8GlcNAc2-PP-Dol (EC 2.4.1.261). | |
| dolichyl-P-Man:Man6GlcNAc2-PP-dolichol α-1,2-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. ALG9 mannosyltransferase catalyses the addition of two different α-1,2-mannose residues - the addition of α-1,2-mannose to Man6GlcNAc2-PP-Dol (EC 2.4.1.259) and the addition of α-1,2-mannose to Man8GlcNAc2-PP-Dol (EC 2.4.1.261). G.Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2489; dolichyl-P-Man:Man6GlcNAc2-PP-dolichol α-1,2-mannosyltransferase; EC 2.4.1.259; ALG9; ALG9 α1,2 mannosyltransferase; dolichylphosphomannose-dependent ALG9 mannosyltransferase; ALG9 mannosyltransferase; Dol-P-Man:Man6GlcNAc2-PP-Dol α-1,2-mannosyltransferase; dolichyl β-D-mannosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?3)-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-1,2-mannosyltransferase. Cat No: EXWM-2489. | |
| dolichyl-P-Man:Man7GlcNAc2-PP-dolichol α-1,6-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. Group: Enzymes. Synonyms: ALG12; ALG12 mannosyltransferase; ALG12 α1,6mannosyltransferase. Enzyme Commission Number: EC 2.4.1.260. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2491; dolichyl-P-Man:Man7GlcNAc2-PP-dolichol α-1,6-mannosyltransferase; EC 2.4.1.260; ALG12; ALG12 mannosyltransferase; ALG12 α1,6mannosyltransferase; dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase; dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl α6-mannosyltransferase; EBS4; Dol-P-Man:Man7GlcNAc2-PP-Dol α-1,6-mannosyltransferase; dolichyl β-D-mannosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-1,6-mannosyltransferase. Cat No: EXWM-2491. | |
| dolichyl-P-Man:Man7GlcNAc2-PP-dolichol α-1,6-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. | |
| dolichyl-P-Man:Man8GlcNAc2-PP-dolichol α-1,2-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. ALG9 mannosyltransferase catalyses the addition of two different α-1,2-mannose residues: the addition of α-1,2-mannose to Man6GlcNAc2-PP-Dol (EC 2.4.1.259) and the addition of α-1,2-mannose to Man8GlcNAc2-PP-Dol (EC 2.4.1.261). Gr. term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2492; dolichyl-P-Man:Man8GlcNAc2-PP-dolichol α-1,2-mannosyltransferase; EC 2.4.1.261; ALG9; ALG9 α1,2 mannosyltransferase; dolichylphosphomannose-dependent ALG9 mannosyltransferase; ALG9 mannosyltransferase; Dol-P-Man:Man8GlcNAc2-PP-Dol α-1,2-mannosyltransferase; dolichyl β-D-mannosyl phosphate:D-Man-α-(1?2)-D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?2)-D-Man-α-(1?3)-[D-Man-α-(1?6)]-D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol 2-α-D-mannosyltransferase. Cat No: EXWM-2492. | |
| dolichyl-P-Man:Man8GlcNAc2-PP-dolichol α-1,2-mannosyltransferase | The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl diphosphate. Early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9Glc-NAc2-PP-Dol on the lumenal side use dolichyl β-D-mannosyl phosphate. ALG9 mannosyltransferase catalyses the addition of two different α-1,2-mannose residues: the addition of α-1,2-mannose to Man6GlcNAc2-PP-Dol (EC 2.4.1.259) and the addition of α-1,2-mannose to Man8GlcNAc2-PP-Dol (EC 2.4.1.261). | |
| dolichyl-xylosyl-phosphate-protein xylosyltransferase | This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. The systematic name of this enzyme class is dolichyl-D-xylosyl-phosphate:protein D-xylosyltransferase. Group: Enzymes. Enzyme Commission Number: EC 2.4.2.33. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2661; dolichyl-xylosyl-phosphate-protein xylosyltransferase; EC 2.4.2.33. Cat No: EXWM-2661. | |
| Dolomite(Calcium Magnesium Carbonate) Powder | Dolomite(Calcium Magnesium Carbonate) Powder. |  CA, FL & NJ |
| Dolutegravir | Dolutegravir (S/GSK1349572) is a highly potent and orally bioavailable HIV integrase strand transfer inhibitor with an IC50 of 2.7 nM for HIV-1 integrase-catalyzed strand transfer. Dolutegravir (S/GSK1349572) inhibits HIV-1 viral replication with an IC50 of 0.51 nM in peripheral blood mononuclear cells. Dolutegravir retains a high potency against the HIV-1 Y143R, N155H, and G140S/Q148H mutants (EC50=3.6-5.8 nM)[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: S/GSK1349572. CAS No. 1051375-16-6. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-13238. | |
| Dolutegravir | Dolutegravir is a two-metal-binding HIV-1 integrase inhibitor with IC50 of 2.7 nM, with modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H. It blocks the strand transfer step of the integration of the viral genome into the host cell (INSTI). Synonyms: GSK-1349572; GSK 1349572; GSK1349572; Tivicay. Grade: ≥98%. CAS No. 1051375-16-6. Molecular formula: C20H19F2N3O5. Mole weight: 419.38. | |
| Dolutegravir | Dolutegravir is a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir is currently in Phase III clinical trials for the treatment of HIV infection. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector. Group: Biochemicals. Alternative Names: (4R, 12aS)-N-[(2, 4-Difluorophenyl)methyl]-3, 4, 6, 8, 12, 12a-hexahydro-7-hydroxy-4-methyl-6, 8-dioxo-2H-pyrido[1', 2':4, 5]pyrazino[2, 1-b][1, 3]oxazine-9-carboxamide; GSK 1349572; S/GSK1349572. Grades: Highly Purified. CAS No. 1051375-16-6. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C20H19F2N3O5, Molecular Weight: 419.38. US Biological Life Sciences. | Worldwide |
| Dolutegravir-[d3] | Dolutegravir-[d3] is a deuterium labelled form of Dolutegravir. Dolutegravir is an antiretroviral medication used to treat HIV/AIDS. Synonyms: (4R,12aS)-N-((2,4-difluorophenyl-3-d)methyl-d2)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide; Dolutegravir D3; Dolutegravir-d3; GSK 1349572-d3; S/GSK1349572-d3; Soltegravir-d3; Tivicay-d3. Grade: 95% by CP; 98% atom D. CAS No. 2673270-25-0. Molecular formula: C20H18D3F2N3O4. Mole weight: 422.42. | |
| Dolutegravir-d5 | Dolutegravir-d5 is used as an internal standard for the quantification of dolutegravir by GC- or LC-MS. Dolutegravir is a potent and orally bioavailable HIV integrase strand transfer inhibitor of HIV integrase. It prevents replication of several HIV-1 strains (EC50s = 0.36-2.1 nM) in peripheral blood mononuclear cells (PBMCs). Synonyms: (4R,12aS)-N-((2,4-difluorophenyl-3,5,6-d3)methyl-d2)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide. Grade: ≥99% atom D. Molecular formula: C20H14D5F2N3O5. Mole weight: 424.41. | |
| Dolutegravir Impurity 1 | Dolutegravir Impurity 1. Uses: For analytical and research use. Alternative Names: (4S,12aS)-7-methoxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylic acid. Molecular formula: C14H16N2O6. Mole weight: 308.29. Catalog: APB05215. | |
| Dolutegravir Impurity 10 | Dolutegravir Impurity 10. Uses: For analytical and research use. Molecular formula: C28H23F4N4NaO6. Mole weight: 610.5. Catalog: APB07650. | |
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