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| Product | Description | |
|---|---|---|
| Dihydrofluorescein diacetate | Dihydrofluorescein diacetate is a chemical used for intracellular staining. Dihydrofluorescein diacetate might be reactive toward a broad range of oxidizing reactions that may be increased during intracellular oxidant stress. Cell-loading studies indicate that dihydrofluorescein achieves higher intracellular concentrations than the other redox sensors such as 2', 7'-dichlorodi hydrofluorescein and Dihydrorhodamine 123. Dihydrofluorescein diacetate is first hydrolyzed by cellular esterases to dihydrofluorescein and is then oxidized to fluorescein primarily by hydrogen peroxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 35340-49-9. Pack Sizes: 500mg, 1000mg. Molecular Formula: C24H18O7, Molecular Weight: 418.4. US Biological Life Sciences. |  Worldwide |
| dihydrofolate reductase | The enzyme from animals and some micro-organisms also slowly reduces folate to 5,6,7,8-tetrahydrofolate. Group: Enzymes. Synonyms: tetrahydrofolate dehydrogenase; DHFR; pteridine reductase:dihydrofolate reductase; dihydrofolate reductase:thymidylate synthase; thymidylate synthetase-dihydrofolate reductase; folic acid reductase; folic reductase; dihydrofolic acid reductase; dihydrofolic reductase; 7,8-dihydrofolate reductase; NADPH-dihydrofolate reductase. Enzyme Commission Number: EC 1.5.1.3. CAS No. 9002-3-3. Dihydrofolate Reductase. 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-1511; dihydrofolate reductase; EC 1.5.1.3; 9002-03-3; tetrahydrofolate dehydrogenase; DHFR; pteridine reductase:dihydrofolate reductase; dihydrofolate reductase:thymidylate synthase; thymidylate synthetase-dihydrofolate reductase; folic acid reductase; folic reductase; dihydrofolic acid reductase; dihydrofolic reductase; 7,8-dihydrofolate reductase; NADPH-dihydrofolate reductase. Cat No: EXWM-1511. |  |
| DIHYDROFOLATE REDUCTASEFROM CHICKEN LIVE R | DIHYDROFOLATE REDUCTASEFROM CHICKEN LIVE R. CAS No. 9002-3-3. |  |
| Dihydrofolate Reductase from human, Recombinant | Dihydrofolate reductase, or DHFR, is an enzyme that reduces dihydrofolic acid to tetrahydrofolic acid, using NADPH as electron donor, which can be converted to the kinds of tetrahydrofolate cofactors used in 1-carbon transfer chemistry. In humans, the DHFR enzyme is encoded by the DHFR gene. It is found in the q11?q22 region of chromosome 5. Bacterial species possesses distinct DHFR enzymes (based on their pattern of binding diaminoheterocyclic molecules), but mammalian DHFRs are highly similar. Human dhfr is an 186 amino acid protein with an apparent molecular weight of 25 kda. it is 30% homologous to the e. coli protein and up to 70% homologous to vertebrate protein. from mycobacterium smegmatis. human dihydrofolate reductase has been used in a study to investigate the stable expression of green fluorescent protein and the targeted disruption of thioredoxin peroxidase-1 gene in babesia bovis. human dihydrofolate reductase has also been used in a study to investigate the structural analysis of human dihydrofolate reductase as a binary complex. Group: Enzymes. Synonyms: DHFR; dihydrofolate reductase; DYR; DHFRP1; Tetrahydrofolate NADP+ oxidoreductase; EC 1.5.1.3; tetrahydrofolate dehydrogenase; pteridine reductase:dihydrofolate reductase; dihydrofolate reductase:thymidylate synthase; thymidylate synthetase-dihydrofolate reductase; f. | |
| dihydrofolate synthase | In some bacteria, a single protein catalyses both this activity and that of EC 6.3.2.17, tetrahydrofolate synthase, the combined activity of which leads to the formation of the coenzyme polyglutamated tetrahydropteroate (H4PteGlun), i.e. various tetrahydrofolates. In contrast, the activities are located on separate proteins in most eukaryotes studied to date. This enzyme is reponsible for attaching the first glutamate residue to dihydropteroate to form dihydrofolate and is present only in those organisms that have the ability to synthesize tetrahydrofolate de novo, e.g. plants, most bacteria, fungi and protozoa. Group: Enzymes. Synonyms: dihydrofolate synthetase; 7,8-dihydrofolate synthetase; H2-folate synthetase; 7,8-dihydropteroate:L-glutamate ligase (ADP); dihydropteroate:L-glutamate ligase (ADP-forming); DHFS. Enzyme Commission Number: EC 6.3.2.12. CAS No. 37318-62-0. 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-5733; dihydrofolate synthase; EC 6.3.2.12; 37318-62-0; dihydrofolate synthetase; 7,8-dihydrofolate synthetase; H2-folate synthetase; 7,8-dihydropteroate:L-glutamate ligase (ADP); dihydropteroate:L-glutamate ligase (ADP-forming); DHFS. Cat No: EXWM-5733. | |
| Dihydrofolic acid | Dihydrofolic acid. Alternative Names: 7,8-Dihydropteroyl-L-glutamic acid Dihydropteroyl-L-glutamic acid; DIHYDROFOLIC ACID. CAS No. 4033-27-6. Purity: 90+%. Product ID: ACM4033276. Molecular formula: C19H21N7O6. Mole weight: 443.41. IUPAC Name: (2S)-2-[[4-[(2-amino-4-oxo-7,8-dihydro-1H-pteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Dihydrogalanthamine hydrobromide | Dihydrogalanthamine hydrobromide is an acetylcholinesterase inhibitor. Dihydrogalanthamine hydrobromide can be used in research on neurological diseases such as sequelae of poliomyelitis and myasthenia gravis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 69353-21-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108723. |  |
| Di(hydrogenated tallowalkyl) methylamines (technical grade) | Di(hydrogenated tallowalkyl) methylamines (technical grade). Alternative Names: Dioctadecyl-hexadecyl methyl amine. CAS No. 61788-63-4. Purity: 95+%. Product ID: ACM61788634-3. Alfa Chemistry - ISO 9001:32057 Certified. | |
| di-(Hydrogenated tallow) benzyl methyl ammonium chloride | di-(Hydrogenated tallow) benzyl methyl ammonium chloride. Alternative Names: di-(Hydrogenated tallow) benzyl methyl ammonium chloride; Benzyl methyl ammonium chloride. CAS No. 61789-73-9. Molecular formula: C8H12ClN. Mole weight: 157.64058. | |
| di-(Hydrogenated tallow-carboxyethyl) hydroxyethyl methyl ammonium methylsulfate | di-(Hydrogenated tallow-carboxyethyl) hydroxyethyl methyl ammonium methylsulfate. Alternative Names: di-(Hydrogenated tallow-carboxyethyl) hydroxyethyl methyl ammonium methylsulfate; di-(Tallow-carboxyethyl) hydroxyethyl methyl ammonium methylsulfate. CAS No. 91995-81-2. | |
| Dihydrogen bis[3-hydroxy-4-(phenylazo)naphthalene-2-carboxylato(2-)]cuprate(2-) | Dihydrogen bis[3-hydroxy-4-(phenylazo)naphthalene-2-carboxylato(2-)]cuprate(2-). Alternative Names: Cuprate(2-),bis(3-hydroxy-4-(phenylazo)-2-naphthalenecarboxylato(2-))-,dihydrogen; EINECS 240-588-8; copper(2+) hydrogen 3-oxido-4-[(e)-phenyldiazenyl]naphthalene-2-carboxylate(1:2:2). CAS No. 16521-34-9. Purity: 96%. Product ID: ACM16521349. Molecular formula: C34H22CuN4O6. Mole weight: 646.107680 [g/mol]. IUPAC Name: copper; hydron; 3-oxido-4-phenyldiazenylnaphthalene-2-carboxylate. ECNumber: 240-588-8. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Dihydrogen Hexachloroiridate (IV) | Dihydrogen Hexachloroiridate (IV). CAS No. 16941-92-7. Pack Sizes: Gram Quantities: 5 gm , 25 gm. Order Number: 1601. |  www.prochemonline.com |
| Dihydrogen Hexachloroplatinate (IV), Pt 40% | Dihydrogen Hexachloroplatinate (IV), Pt 40%. Grades: 99.99% Extremely High (>=99%). CAS No. 16941-12-1. Pack Sizes: Gram Quantities: 5 gm , 25 gm. Order Number: 1602. | www.prochemonline.com |
| Dihydrogen hexahydroxyplatinate | Dihydrogen hexahydroxyplatinate. Alternative Names: Hydrogen hexahydroxyplatinate(IV). CAS No. 51850-20-5. Molecular formula: H8O6Pt. Mole weight: 299.14. Purity: 98%. IUPAC Name: hydron; platinum; hexahydroxide. |  |
| Dihydrogen hexahydroxyplatinate (IV) | Dihydrogen hexahydroxyplatinate (IV). Group: Biochemicals. Alternative Names: Hexahydroxoplatinic (IV) acid. Grades: Highly Purified. CAS No. 51850-20-5. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Dihydrogen hexahydroxyplatinate (IV) ≥85%, (55% Platinum content | Dihydrogen hexahydroxyplatinate (IV) ≥85%, (55% Platinum content. Group: Biochemicals. Grades: Reagent Grade. CAS No. 51850-20-5. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| dihydrogen phosphate; (2-phenylpropylamino)azanium | dihydrogen phosphate; (2-phenylpropylamino)azanium. CAS No. 16602-80-5. Product ID: ACM16602805. Molecular formula: C9H17N2O4P. Mole weight: 248.216 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl4-amino-2-butoxybenzoate | Dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl4-amino-2-butoxybenzoate. Alternative Names: WIN 3502, 4-Amino-2-butoxy-benzoic acid 3-piperidinopropyl ester hydrogen phosphate, BENZOIC ACID, 4-AMINO-2-BUTOXY-, 3-PIPERIDINOPROPYL ESTER, HYDROGEN PHOSPHATE, AC1L1O4Z, AC1Q22I4, LS-35649, 1-{3-[(4-amino-2-butoxybenzoyl)oxy]propyl}piperidinium dihydrogen phosphate, dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl 4-amino-2-butoxybenzoate, 100811-78-7. CAS No. 100811-78-7. Purity: 96%. Product ID: ACM100811787. Molecular formula: C19H33N2O7P. Mole weight: 432.448 g/mol. IUPAC Name: dihydrogen phosphate;3-piperidin-1-ium-1-ylpropyl 4-amino-2-butoxybenzoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl4-amino-2-phenylmethoxybenzoate | Dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl4-amino-2-phenylmethoxybenzoate. Alternative Names: WIN 3503, 4-Amino-2-(benzyloxy)benzoic acid 3-piperidinopropyl ester hydrogen phosphate, Benzoic acid, 4-amino-2-(benzyloxy)-, 3-piperidinopropyl ester, hydrogen phosphate, AC1L1NRW, AC1Q22I5, LS-35626, 1-(3-{[4-amino-2-(benzyloxy)benzoyl]oxy}propyl)piperidiniumdihydrogen phosphate, dihydrogen phosphate; 3-piperidin-1-ium-1-ylpropyl 4-amino-2-phenylmethoxybenzoate, 100347-84-0. CAS No. 100347-84-0. Purity: 96%. Product ID: ACM100347840. Molecular formula: C22H31N2O7P. Mole weight: 466.465 g/mol. IUPAC Name: dihydrogen phosphate;3-piperidin-1-ium-1-ylpropyl 4-amino-2-phenylmethoxybenzoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Dihydrogranaticin B | Produced by the strain of Streptomyces thermoviolaceus subsp. pigenes var. WR-141. It is a red pigment with activity against Bacillus cereus. Molecular formula: C28H32O12. Mole weight: 560.55. | |
| Dihydrohypothemycin | It is produced by the strain of Hypomyces trichothecoides. Dihydrohypothemycin has anti-tsutsugamushi activity. Molecular formula: C10H24O8. Mole weight: 272.29. | |
| Dihydro Ionone Beta | Dihydro Ionone Beta. CAS No. 17283-81-7. FEMA No. 3626. Kosher: Y. VIGON Item # 501420. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Dihydro isoferulic acid 3-O-sulfate | Dihydro isoferulic acid 3-O-sulfate. Group: Biochemicals. Alternative Names: 4-Methoxy-3- (sulfooxy) benzenepropanoic acid; Dihydroisoferulic acid 3-O-sulfate. Grades: Highly Purified. CAS No. 1258842-21-5. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H12O7S. US Biological Life Sciences. | Worldwide |
| Dihydro Isoferulic Acid-d3 3-O- β-D-Glucuronide | Labeled Dihydroisoferulic Acid 3-O- β-D-Glucuronide, the glucuronide conjugate of Dihydroisoferulic Acid. Dihydroisoferulic Acid 3-O- β-D-Glucuronide is a minor circulating metabolite in human plasma after ingestion of coffee and can be used as a biomarker of coffee consumption. Group: Biochemicals. Alternative Names: 5-(2-Carboxyethyl)-2-(methox-d3)yphenyl β-D-Glucopyranosiduronic Acid; Dihydroisoferulic Acid-d3 3-O-Glucuronide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Dihydro Isoferulic Acid-d3 3-O-Sulfate Disodium Salt | Labeled Dihydroisoferulic Acid 3-O-Sulfate, the sulfate conjugate of Dihydroisoferulic Acid. Dihydroisoferulic Acid 3-O-Sulfate is a minor circulating metabolite in human plasma after coffee consumption. Group: Biochemicals. Alternative Names: 4- (Methoxy-d3) -3- (sulfooxy) benzenepropanoic Acid Disodium; Dihydroisoferulic Acid-d3 3-O-Sulfate Disodium Salt. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Dihydroisojasmone | Dihydroisojasmone. Alternative Names: 2-hexyl-2-cyclopenten-1-on; 2-n-hexyl-2-cyclopenten-1-one; 2-HEXYL-2-CYCLOPENTEN-1-ONE; 2-HEXYL-2-CYCLOPENTENONE; 2-HEXYLCYCLOPENT-2-EN-1-ONE; 2-HEXYL-CYCLOPENT-2-ENONE; DIHYDROISOJASMONE; FEMA 3552. Grades: 96%. CAS No. 95-41-0. Molecular formula: C11H18O. Mole weight: 166.26. | |
| DIHYDROJASMONE | Dihydrojasmone, a synthetic fragrance compound widely utilized in the biomedicine sector due to its acclaimed anti-inflammatory and anti-cancer attributes, exhibits notable potential in the treatment of skin ailments and as a prospective therapeutic intervention for specific cancer variations. Alternative Names: 2-Cyclopenten-1-one, 3-methyl-2-pentyl-, DIHYDROJASMONE. Grades: 99.0%. CAS No. 1128-08-1. Molecular formula: C11H18O. Mole weight: 166.27. | |
| Dihydrokaempferol | Dihydrokaempferol is isolated from Bauhinia championii (Benth). Dihydrokaempferol induces apoptosis and inhibits Bcl-2 and Bcl-xL expression. Dihydrokaempferol is a good candidate for new antiarthritic agents[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 480-20-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N2897. | |
| Dihydrokainic acid | Dihydrokainic acid. Group: Biochemicals. Grades: Purified. CAS No. 52497-36-6. Pack Sizes: 1mg, 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Dihydrokavain | Dihydrokavain is a kavalactone source from kava beverages used in herbal medicine to treat sleep disturbances, as well as stress and anxiety. Uses: Used in herbal medicine to treat sleep disturbances, as well as stress and anxiety. Alternative Names: (2S)-4-methoxy-2-(2-phenylethyl)-2,3-dihydropyran-6-one; (+)-(S)-Dihydrokavain; 7,8-Dihydrokawain. Grades: ≥95%. CAS No. 587-63-3. Molecular formula: C14H16O3. Mole weight: 232.28. | |
| Dihydrokavain | Dihydrokavain. Group: Biochemicals. CAS No. 587-63-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Dihydrokawain | Botanical Source: Group: Biochemicals. Alternative Names: Marindinin. Grades: Plant Grade. CAS No. 587-63-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Dihydro Ketoprofen (Mixture of Diastereomers) | A metabolite of Ketoprofen. Group: Biochemicals. Alternative Names: 3-(Hydroxyphenylmethyl)-α-methylbenzeneacetic Acid; Dihydroketoprofen. Grades: Highly Purified. CAS No. 59960-32-6. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| dihydrolanosterol-d7 | dihydrolanosterol-d7. Group: Others. Purity: >98%. Mole weight: 435.776. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; dihydrolanosterol-d7; 25,26,26,26,27,27,27-heptadeuteriolanost-8-en-3ss-ol. Cat No: STEZ-021. | |
| Dihydrolinalool | Dihydrolinalool. CAS No. 18479-51-1. Kosher: Y. VIGON Item # 502553. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| dihydrolipoyl dehydrogenase | A flavoprotein (FAD). A component of the multienzyme 2-oxo-acid dehydrogenase complexes. In the pyruvate dehydrogenase complex, it binds to the core of EC 2.3.1.12, dihydrolipoyllysine-residue acetyltransferase, and catalyses oxidation of its dihydrolipoyl groups. It plays a similar role in the oxoglutarate and 3-methyl-2-oxobutanoate dehydrogenase complexes. Another substrate is the dihydrolipoyl group in the H-protein of the glycine-cleavage system (click here for diagram), in which it acts, together with EC 1.4.4.2, glycine dehydrogenase (decarboxylating), and EC 2.1.2.10, aminomethyltransferase, to break down glycine. It can also use free dihydrolipoate, dihydrolipoamide or.tase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; protein-6-N-(dihydrolipoyl)lysine:NAD+ oxidoreductase. Enzyme Commission Number: EC 1.8.1.4. CAS No. 9001-18-7. Diaphorase. 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-1648; dihydrolipoyl dehydrogenase; EC 1.8.1.4; 9001-18-7; LDP-Glc; LDP-Val; dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxido. | |
| dihydrolipoyllysine-residue (2-methylpropanoyl)transferase | A multimer (24-mer) of this enzyme forms the core of the multienzyme 3-methyl-2-oxobutanoate dehydrogenase complex, and binds tightly both EC 1.2.4.4, 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively 2-methylpropanoylated by EC 1.2.4.4, and the only observed direction catalysed by EC 2.3.1.168 is that where this 2-methylpropanoyl is passed to coenzyme A. In addition to the 2-methylpropanoyl group, formed when EC 1.2.4.4 acts on the oxoacid that corresponds with valine, this enzyme also transfers the 3-methylbutanoyl and S-2-methylbutanoyl groups, donated to it when EC 1.2.4.4 acts on the oxo acids corresponding with leucine and isoleucine. Group: Enzymes. Synonyms: dihydrolipoyl transacylase; enzyme-dihydrolipo. Enzyme Commission Number: EC 2.3.1.168. CAS No. 102784-26-9. 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-2108; dihydrolipoyllysine-residue (2-methylpropanoyl)transferase; EC 2.3.1.168; 102784-26-9; dihydrolipoyl transacylase; enzyme-dihydrolipoyllysine:2-methylpropanoyl-CoA S-(2-methylpropanoyl)transferase; 2-methylpropanoyl-CoA:enzyme-6-N-(dihydrolipoyl)lysine S-(2-methylpropanoyl)transferase. Cat No: EXWM-2108. | |
| dihydrolipoyllysine-residue acetyltransferase | A multimer (24-mer or 60-mer, depending on the source) of this enzyme forms the core of the pyruvate dehydrogenase multienzyme complex, and binds tightly both EC 1.2.4.1, pyruvate dehydrogenase (acetyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively acetylated by EC 1.2.4.1, and the only observed direction catalysed by EC 2.3.1.12 is that where the acetyl group is passed to coenzyme A. Group: Enzymes. Synonyms: acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; d. Enzyme Commission Number: EC 2.3.1.12. CAS No. 9032-29-5. 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-2058; dihydrolipoyllysine-residue acetyltransferase; EC 2.3.1.12; 9032-29-5; acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; dihydrolipoate acetyltransferase; dihydrolipoic transacetylase; dihydrolipoyl acetyltransferase; lipoate acetyltransferase; lipoate transacetylase; lipoic acetyltransferase; lipoic acid acetyltransferase; lipoic transacetylase; lipoylacetyltransferase; thioltransacetylase A; transacetylase X; enzyme-dihydrolipoyllysine:acetyl-CoA S-acetyltransferase; acetyl-CoA:enzyme 6-N-(dihydrolipoyl)lysine S-acetyltransferase. Cat No: EXWM-2058. | |
| dihydrolipoyllysine-residue succinyltransferase | A multimer (24-mer) of this enzyme forms the core of the multienzyme complex, and binds tightly both EC 1.2.4.2, oxoglutarate dehydrogenase (succinyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively succinylated by EC 1.2.4.2, and the only observed direction catalysed by EC 2.3.1.61 is that where this succinyl group is passed to coenzyme A. Group: Enzymes. Synonyms: dihydrolipoamide S-succinyltransferase; dihydrolipoamide succinyltransferase; dihydrolipoic transsuccinylase; dihydrolipolyl transsuccinylase; dihydrolipoyl transsuccinylase; lipoate succinyltrans. Enzyme Commission Number: EC 2.3.1.61. CAS No. 9032-28-4. 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-2241; dihydrolipoyllysine-residue succinyltransferase; EC 2.3.1.61; 9032-28-4; dihydrolipoamide S-succinyltransferase; dihydrolipoamide succinyltransferase; dihydrolipoic transsuccinylase; dihydrolipolyl transsuccinylase; dihydrolipoyl transsuccinylase; lipoate succinyltransferase (Escherichia coli); lipoic transsuccinylase; lipoyl transsuccinylase; succinyl-CoA:dihydrolipoamide S-succinyltransferase; succinyl-CoA:dihydrolipoate S-succinyltransferase; enzyme-dihydrolipoyllysine:succinyl-CoA S-succinyltransferase. Cat No: EXWM-2241. | |
| Dihydrolycorine | Dihydrolycorine. Group: Biochemicals. Grades: Plant Grade. CAS No. 6271-21-2. Pack Sizes: 20mg. Molecular Formula: C16H19NO4, Molecular Weight: 289.33. US Biological Life Sciences. | Worldwide |
| Dihydromaitophilin | Dihydromaitophilin has the ability of anti-plasmopara viticola. Molecular formula: C29H40N2O6. Mole weight: 512.64. | |
| dihydromethanopterin reductase (acceptor) | This archaeal enzyme catalyses the last step in the biosynthesis of tetrahydromethanopterin, a coenzyme used in methanogenesis. The enzyme, characterized from the archaea Methanosarcina mazei and Methanocaldococcus jannaschii, is an iron-sulfur flavoprotein. cf. EC 1.5.1.47, dihydromethanopterin reductase [NAD(P)+]. Group: Enzymes. Synonyms: DmrX. Enzyme Commission Number: EC 1.5.99.15. 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-1569; dihydromethanopterin reductase (acceptor); EC 1.5.99.15; DmrX. Cat No: EXWM-1569. | |
| dihydromethanopterin reductase [NAD(P)+] | The enzyme, characterized from the bacterium Methylobacterium extorquens, is involved in biosynthesis of dephospho-tetrahydromethanopterin. The specific activity with NADH is 15% of that with NADPH at the same concentration. It does not reduce 7,8-dihydrofolate (cf. EC 1.5.1.3, dihydrofolate reductase). Group: Enzymes. Synonyms: DmrA; H2MPT reductase; 5,6,7,8-tetrahydromethanopterin 5,6-oxidoreductase; dihydromethanopterin reductase. Enzyme Commission Number: EC 1.5.1.47. 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-1528; dihydromethanopterin reductase [NAD(P)+]; EC 1.5.1.47; DmrA; H2MPT reductase; 5,6,7,8-tetrahydromethanopterin 5,6-oxidoreductase; dihydromethanopterin reductase. Cat No: EXWM-1528. | |
| Dihydromethysticin | Dihydromethysticin. Group: Biochemicals. Alternative Names: ?-Methysticin; Pseudomethysticin. Grades: Plant Grade. CAS No. 19902-91-1. Pack Sizes: 10mg. Molecular Formula: C15H16O5, Molecular Weight: 276.285. US Biological Life Sciences. | Worldwide |
| Dihydromevinolin | Dihydromevinolin is an impurity in Lovastatin bulk drug. It is produced by the strain of Aspergollus terreus. Alternative Names: 4a,5-Dihydro Lovastatin; (2S)-2-Methylbutanoic Acid (1S,3S,4aR,7S,8S,8aS)-1,2,3,4,4a,7,8,8a-Octahydro- 3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl Ester; (+)-Dihydromevinolin; Dihydrolovastatin; Dihydromevinol. Grades: > 95%. CAS No. 77517-29-4. Molecular formula: C24H38O5. Mole weight: 406.56. | |
| Dihydromocimycin | It is produced by the strain of Streptomyces namocissimus. Molecular formula: C43H62N2O10. Mole weight: 766.96. | |
| Dihydromonacolin L | Dihydromonacolin L is produced by the strain of Monascus ruber. The IC50 of HMG-CO reductase was 4.1 μmol/L. Alternative Names: dihydromonacolin L lactone. CAS No. 86827-77-2. Molecular formula: C19H30O3. Mole weight: 306.44. | |
| dihydromonacolin L hydroxylase | A heme-thiolate protein (cytochrome P-450). The dehydration of 3α-hydroxy-3,5-dihydromonacolin L acid is believed to be spontaneous. The enzyme from fungi also catalyses the reaction of EC 1.14.13.198, monacolin L hydroxylase. Group: Enzymes. Synonyms: LovA (ambiguous). Enzyme Commission Number: EC 1.14.13.197. 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-0797; dihydromonacolin L hydroxylase; EC 1.14.13.197; LovA (ambiguous). Cat No: EXWM-0797. | |
| dihydromonacolin L-[lovastatin nonaketide synthase] thioesterase | Dihydromonacolin L acid is synthesized while bound to an acyl-carrier protein domain of the lovastatin nonaketide synthase (EC 2.3.1.161). Since that enzyme lacks a thioesterase domain, release of the dihydromonacolin L acid moiety from the polyketide synthase requires this dedicated enzyme. Group: Enzymes. Synonyms: LovG. Enzyme Commission Number: EC 3.1.2.31. GUSB. 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-3565; dihydromonacolin L-[lovastatin nonaketide synthase] thioesterase; EC 3.1.2.31; LovG. Cat No: EXWM-3565. | |
| dihydromonapterin reductase | The enzyme, found in many Gram negative bacteria, also slowly reduces 7,8-dihydrofolate to 5,6,7,8-tetrahydrofolate (cf. EC 1.5.1.3, dihydrofolate reductase). The enzyme has no activity with NADH. Group: Enzymes. Synonyms: FolM; H2-MPt reductase. Enzyme Commission Number: EC 1.5.1.50. 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-1532; dihydromonapterin reductase; EC 1.5.1.50; FolM; H2-MPt reductase. Cat No: EXWM-1532. | |
| Dihydro Montelukast Sodium Salt | A Montelukast impurity. A saturated hydroxyalkylquinoline acid as leukotriene antagonist and biosynthesis inhibitor. Group: Biochemicals. Alternative Names: (R) -1- [ [ [1- [3- [2- (7-Chloro-2-quinolinyl) ethyl] phenyl] -3- [2- (1-hydroxy-1-methylethyl) phenyl] propyl] thio] methyl] cyclopropaneacetic Acid Monosodium Salt. Grades: Highly Purified. CAS No. 142147-98-6. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. | Worldwide |
| Dihydromorin | Dihydromorin, a natural flavanonol compound, is a tyrosinase inhibitor[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 18422-83-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N3748. | |
| Dihydromorin | Dihydromorin is a flavonoid isolated from the branch of Morus alba L. Alternative Names: 2',3,4',5,7-pentahydroxyflavanone; (2R,3R)-2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxychroMan-4-one. Grades: 90%. CAS No. 18422-83-8. Molecular formula: C15H12O7. Mole weight: 304.25. | |
| Dihydromunduletone | Dihydromunduletone (DHM) is a rotenoid derivative and a selective, potent adhesion G protein-coupled receptor (aGPCR) (GPR56 and GPR114/ADGRG5) antagonist with an IC 50 of 20.9 μM for GPR56, but not inhibit GPR110 or class A GPCRs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 674786-20-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101483. | |
| Dihydro mupirocin | Dihydro mupirocin. Group: Biochemicals. Grades: Highly Purified. CAS No. 1246812-11-2. Pack Sizes: 10mg, 25mg. Molecular Formula: C26H46O9. US Biological Life Sciences. | Worldwide |
| Dihydromycochromenic acid | Dihydromycochromenic acid. Molecular formula: C17H20O6. Mole weight: 320.34. | |
| Dihydromyrcene | Dihydromyrcene (CAS# 2436-90-0 ) is a useful research chemical. Alternative Names: (+)-β-citronellene; 1,6-Octadiene, 3,7-dimethyl-; 1,6-octadiene, 3,7-dimethyl-, S(+)-; 3,7-dimethyl-6-octadiene; 3,7-Dimethyl-octa-1,6-diene. Grades: 95 %. CAS No. 2436-90-0. Molecular formula: C10H18. Mole weight: 138.25. | |
| dihydromyrcenol | dihydromyrcenol (CAS# 18479-58-8) is used in preparation method of orange flavor essence, and its application in daily chemical product. Alternative Names: 2,6-dimethyloct-7-en-2-ol. Grades: 95 %. CAS No. 18479-58-8. Molecular formula: C10H20O. Mole weight: 156.27. | |
| Dihydromyrcenol | Dihydromyrcenol. CAS No. 18479-58-8. Kosher: Y. VIGON Item # 500111. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Dihydromyricetin | Ampelopsin is a flavanonol isolated from the herb of Myrica rubra (Lour.)Zucc., exhibiting antioxidant, antiproliferative, anti-apoptotic, and anti-alcohol intoxication properties. Ampelopsin is a natural compound used in cosmetics material. It can improve the skin barrier and has multiple effects such as anti-aging and removing wrinkles, whitening and lightening spots, soothing repair, anti-inflammatory, and antibacterial. In addition, it has the effect of healing wounds and nursing hair. Uses: Food, health care products. Alternative Names: Ampelopsis Grossedentata Extract; Water-Soluble Dihydromyricetin; (2R,3R)-2,3-Dihydro-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-, (2R-trans)-; Ampelopsin; Flavanone, 3,3',4',5,5',7-hexahydroxy-; (+)-Ampelopsin; (+)-Dihydromyricetin; Ampelopsin (flavanol); Ampeloptin; REL-Eqyms 98. Grades: 95%. CAS No. 27200-12-0. Molecular formula: C15H12O8. Mole weight: 320.25. | |
| Dihydromyricetin | Dihydromyricetin is a potent inhibitor with an IC50 of 48 μM on dihydropyrimidinase. Dihydromyricetin can activate autophagy through inhibiting mTOR signaling. Dihydromyricetin suppresses the formation of mTOR complexes (mTORC1/2). Dihydromyricetin is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 22 μM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ampelopsin; Ampeloptin. CAS No. 27200-12-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-N0112. | |
| Dihydromyricetin, Food Grade | Ampeloptin is an antioxidant and a competitive GABAA antagonist (1,2,3). Ampeloptin competitively inhibits the benzodiazepine site and induces autophagy and shows antiproliferative effects. Group: Biochemicals. Alternative Names: (2R,3R)-2,3-Dihydro-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one; (2R-trans)-2,3-Dihydro-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one; Ampelopsin; 3,3,4,5,5,7-Hexahydroxy-flavanone; (+)-Ampelopsin; (+)-Dihydromyricetin; Ampelopsin (flavanol); Dihydromyricetin. Grades: Plant Grade. CAS No. 27200-12-0. Pack Sizes: 100g, 500g, 1Kg. Molecular Formula: C??H??O?, Molecular Weight: 320.25. US Biological Life Sciences. | Worldwide |
| Dihydro-N-Caffeoyltyramine | An impurity of Tyramine. Tyramine is a catecholamine releasing agent that binds to both TAAR1 and TAAR2 as an agonist. Tyramine is derived from Tyrosine. Alternative Names: Benzenepropanamide, 3,4-dihydroxy-N-[2-(4-hydroxyphenyl)ethyl]-; 3,4-Dihydroxy-N-[2-(4-hydroxyphenyl)ethyl]benzenepropanamide; N-(4-Hydroxyphenethyl)-3-(3,4-dihydroxyphenyl)propanamide; Dihydro-N-Caffeoyl Tyramine. CAS No. 501939-19-1. Molecular formula: C17H19NO4. Mole weight: 301.35. | |
| Dihydroneopterin | Dihydroneopterin. Group: Biochemicals. Alternative Names: 2-Amino-7,8-dihydro-6-[(1S,2R)-1,2,3-trihydroxypropyl]-4(3H)-pteridinone; D-Erythro-1-(2-amino-7,8-dihydro-4-hydroxy-6-pteridinyl)-1,2,3-propanetrio; [S-(R*,S*)]-2-Amino-7,8-dihydro-6-(1,2,3-trihydroxypropyl)-4(1H)-pteridinone; 2-Amino-7,8-dihydro-6-[(1S,2R)-1,2,3-trihydroxypropyl]-4(1H)-pteridinone; 2-Amino-4-hydroxy-6-(D-erythro-1,2,3-trihydroxypropyl)-7,8-dihydropteridine; 2-Amino-4-hydroxy-6-(D-erythro-1',2',3'-trihydroxypropyl)-7,8-dihydropteridine; 7,8-Dihydro-D-erythro-neopterin; 7,8-Dihydro-D-neopterin; 7,8-Dihydroneopterin; D-erythro-7,8-Dihydroneopterin. Grades: Highly Purified. CAS No. 1218-98-0. Pack Sizes: 25mg. Molecular Formula: C9H13N5O4, Molecular Weight: 255.23. US Biological Life Sciences. | Worldwide |
| dihydroneopterin aldolase | The enzyme participates in folate (in bacteria, plants and fungi) and methanopterin (in archaea) biosynthesis. The enzymes from the bacterium Escherichia coli and the plant Arabidopsis thaliana also catalyse the epimerisation of the 2' hydroxy-group (EC 5.1.99.8, 7,8-dihydroneopterin epimerase). The enzyme from the bacterium Mycobacterium tuberculosis is trifunctional and also catalyses EC 5.1.99.8 and EC 1.13.11.81, 7,8-dihydroneopterin oxygenase. The enzyme from the yeast Saccharomyces cerevisiae also catalyses the two subsequent steps in the folate biosynthesis pathway - EC 2.7.6.3, 2-amino-4-hydroxy-6-(hydroxymethyl)dihydropteridine diphosphokinase, and EC 2.5.1.15, dihydropteroate synthase. Group: Enzymes. Synonyms: 7,8-dihydroneopterin aldolase; 2-amino-. Enzyme Commission Number: EC 4.1.2.25. CAS No. 37290-59-8. 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-4864; dihydroneopterin aldolase; EC 4.1.2.25; 37290-59-8; 7,8-dihydroneopterin aldolase; 2-amino-4-hydroxy-6-(D-erythro-1,2,3-trihydroxypropyl)-7,8-dihydropteridine glycolaldehyde-lyase; 2-amino-4-hydroxy-6-(D-erythro-1,2,3-trihydroxypropyl)-7,8-dihydropteridine glycolaldehyde-lyase (2-amino-4-hydroxy-6-hydroxymethyl-7,8-dihydropteridine-forming); DHNA; mptD (gene name); folB (gene name). Cat No: EXWM-4864. | |
| dihydroneopterin triphosphate 2'-epimerase | The enzyme, found in gammaproteobacteria, has almost no activity with 7,8-dihydroneopterin. Group: Enzymes. Synonyms: D-erythro-7,8-dihydroneopterin triphosphate epimerase; folX (gene name). Enzyme Commission Number: EC 5.1.99.7. 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-5439; dihydroneopterin triphosphate 2'-epimerase; EC 5.1.99.7; D-erythro-7,8-dihydroneopterin triphosphate epimerase; folX (gene name). Cat No: EXWM-5439. | |
| dihydroneopterin triphosphate diphosphatase | The enzyme participates in a folate biosynthesis pathway, which is found in bacteria, fungi, and plants. Requires Mg2+. Group: Enzymes. Synonyms: folQ (gene name); nudB (gene name); NUDT1 (gene name); dihydroneopterin triphosphate pyrophosphohydrolase. Enzyme Commission Number: EC 3.6.1.67. 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-4640; dihydroneopterin triphosphate diphosphatase; EC 3.6.1.67; folQ (gene name); nudB (gene name); NUDT1 (gene name); dihydroneopterin triphosphate pyrophosphohydrolase. Cat No: EXWM-4640. | |
| Dihydronicotinamide Adenine Dinucleotide | Dihydronicotinamide Adenine Dinucleotide (NADH) is a vital coenzyme in the biomedicine industry. Widely used in cellular respiration, NADH plays a crucial role in transferring electrons during metabolic reactions. Alternative Names: 1,4-Dihydronicotinamide adenine dinucleotide; beta-DPNH; beta-NADH. Grades: 95%. CAS No. 58-68-4. Molecular formula: C21H29N7O14P2. Mole weight: 665.4. | |
| Dihydronicotinamide riboside | Dihydronicotinamide riboside is a potent NAD+ concentration enhancer. Dihydronicotinamide riboside modulates targets BAX, PUMA, NQO2, and IκB kinase. Dihydronicotinamide riboside mediates apoptosis, induces pro-oxidant activity, mitochondrial dysfunction, metabolic dysregulation, redox modulation, and pro-inflammatory M1 phenotype induction. Dihydronicotinamide riboside increases intracellular and mitochondrial NAD+ levels, maintains cell survival against NAD+-depleting genotoxins. Dihydronicotinamide riboside can be used for the research of hepatocellular carcinoma[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 19132-12-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W614507. | |
| Dihydro Nicotyrine | Dihydro Nicotyrine. Group: Biochemicals. Alternative Names: 3-(4,5-Dihydro-1-methyl-1H-pyrrol-2-yl)pyridine; 3-(4,5-Dihydro-1-methylpyrrol-2-yl)pyridine. Grades: Highly Purified. CAS No. 525-74-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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