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| Product | Description | |
|---|---|---|
| Luciferase from Photinus pyralis (firefly), Recombinant | Firefly luciferase is an enzyme that catalyzes production of light from luciferin in the presence of Mg2+-ATP and oxygen. The reaction of this enzyme with luciferin, ATP, and O2 results in the emission of light. Luciferase activity can be inhibited by general anesthetics including isoflurane and ketamine/medetomidine thereby affecting the sensitivity of bioluminescence imaging. Applications: The reaction of this enzyme with luciferin, atp, and o2 results in the emission of light. luciferase can be used to detect trace amounts of atp. firefly luciferase is also one of the most commonly utilized reporter genes for the study of gene expression. the bioluminescent rea.pe I , > 5 ,000 ,000 units/mg protein; Type II, 15-30×106 light units/mg protein. Storage: -70°C. Form: Type I, Supplied as a solution in 50 mM Tris HCl pH 8.0, 1 mM dithiothreitol, 1 mM EDTA, and 10% (v/v) glycerol; Type II, Lyophilized powder approximately 20% protein; balance is primarily NaCl, HEPES buffer salts, and carbohydrate. Source: E. coli. Species: Photinus pyralis (firefly). Photinus-luciferin 4-monooxygenase (ATP-hydrolysing); firefly luciferase; luciferase (firefly luciferin); Photinus luciferin 4-monooxygenase (adenosine triphosphate-hydrolyzing); firefly luciferin luciferase; Photinus pyralis luciferase; EC 1.13.12.7; 61970-00-1. Cat No: NATE-0424. |  |
| Luciferase from Vibrio fischeri | Luciferase from Vibrio fischeri. Group: Biochemicals. Grades: Highly Purified. CAS No. 9014-00-0. Pack Sizes: 100mg, 250mg, 500mg. US Biological Life Sciences. |  Worldwide |
| Luciferase from Vibrio fischeri (Photobacterium f) | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Luciferase-IN-4 | Luciferase-IN-4 (Compound 6b) is an inhibitor for luciferase with IC 50 of 4.1 μM. Luciferase-IN-4 inhibits purified luciferase in P. pyralis with IC 50 of 2.0 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1020413-85-7. Pack Sizes: 1 mg. Product ID: HY-161475. |  |
| Lucifer Yellow CH dilithium salt | fluorescent stain. Group: Fluorescence/luminescence spectroscopy. | |
| Lucifer Yellow CH dipotassium salt | Lucifer Yellow CH dipotassium is a high-intensity fluorescent probe containing free hydrazyl groups. Lucifer Yellow CH can react with fatty aldehydes at room temperature. Lucifer Yellow CH serves as a biological tracer to monitor neuronal branching, regeneration, gap junction detection and characterization, and selective ablation of cells after aldehyde fixation. Lucifer yellow CH displays the maximum excitation/emission of 430 nm/540 nm, respectively [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 71206-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-W127715. | |
| Lucifer Yellow CH dipotassium salt | powder. Group: Fluorescence/luminescence spectroscopy. | |
| Lucifer yellow vs dilithium salt | Lucifer yellow vs dilithium salt. Group: Bioelectronic materials other materials. Alternative Names: 4-AMINO-N-[3- (VINYLSULFONYL)-PHENYL]NAPHTHALIMIDE-3, 6-DISULFONATE DILITHIUM SALT; LUCIFER YELLOW VS; LUCIFER YELLOW VS DILITHIUM SALT; DILITHIUM 4-AMINO-N-[3- (VINYLSULFONYL)PHENYL]NAPHTHALIMIDE-3, 6-DISULFONATE; LUCIFER YELLOW VS DILITHIUM SALT, FOR FL UORESCE. CAS No. 71231-14-6. Product ID: dilithium; 6-amino-2-(3-ethenylsulfonylphenyl)-1,3-dioxobenzo[de]isoquinoline-5,8-disulfonate. Molecular formula: 550.5g/mol. Mole weight: C20H12Li2N2O10S3. [Li+]. [Li+]. C=CS (=O) (=O)C1=CC=CC (=C1)N2C (=O)C3=CC (=CC4=C3C (=CC (=C4N)S (=O) (=O)[O-])C2=O)S (=O) (=O)[O-]. InChI=1S/C20H14N2O10S3. 2Li/c1-2-33 (25, 26)11-5-3-4-10 (6-11)22-19 (23)14-8-12 (34 (27, 28)29)7-13-17 (14)15 (20 (22)24)9-16 (18 (13)21)35 (30, 31)32; ; /h2-9H, 1, 21H2, (H, 27, 28, 29) (H, 30, 31, 32); ; /q; 2*+1/p-2. PSJNJVOFDDMXDP-UHFFFAOYSA-L. |  |
| Lucigenin | Lucigenin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N'-Dimethyl-9,9'-biacridiniumdinitrate. Product Category: Other Fluorophores. Appearance: Off-white to brown powder. CAS No. 2315-97-1. Molecular formula: C28H22N4O6. Mole weight: 510.5. Purity: 98%+. IUPACName: 10-methyl-9-(10-methylacridin-10-ium-9-yl)acridin-10-ium;dinitrate. Canonical SMILES: C[N+]1=C2C=CC=CC2=C(C3=CC=CC=C31)C4=C5C=CC=CC5=[N+](C6=CC=CC=C64)C.[N+](=O)([O-])[O-].[N+](=O)([O-])[O-]. Product ID: ACM2315971-1. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Lucigenin | Lucigenin is a chemiluminescence probe. Lucigenin can be used to detect the production of endogenous superoxide anion radical (O 2- ). Lucigenin is extremely sensitive to chloride ions, while it combined with chloride ions, the fluorescence will be quenched. Lucigenin also can be used as a chloride indicator. Ex/Em=455/505 nm [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: NSC-151912; L-6868. CAS No. 2315-97-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-D0720. | |
| Lucilactaene | It is produced by the strain of Fusarium sp. RK-97-94. It is a P53-transfected tumor cell cycle inhibitor. It inhibits the cell cycle progression of H1299/TSP53 in G1 phase. Molecular formula: C22H27NO6. Mole weight: 401.45. |  |
| Lucilin, partial | Lucilin, partial was found in Lucilia sericata [Green bottle fly] and has antimicrobial activity. Grade: >96% by HPLC. | |
| Lucitanib | Lucitanib (E-3810) is a novel dual inhibitor of VEGFR and FGFR , potently and selectively inhibits VEGFR1 , VEGFR2 , VEGFR3 , FGFR1 and FGFR2 with IC 50 s of 7 nM, 25 nM, 10 nM, 17.5 nM, and 82.5 nM, respectively [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E-3810. CAS No. 1058137-23-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15391. | |
| lucPpy-IN-1 | lucPpy-IN-1 (compound 9) is an ATP-dependent luciferase from Photinus pyralis ( lucPpy ) inhibitor with an IC 50 value of 4.0 μM. lucPpy-IN-1 can be used for the research of targets agentgability [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 546100-66-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148407. | |
| Lucyoside B | Lucyoside B. Group: Biochemicals. CAS No. 91174-19-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| LUF5834 | LUF5834 is a selective A 2B adenosine receptor ( A2BR ) partial agonist ( EC 50 = 12 nM). LUF5834 is also a partial A 1 /A 2A adenosine receptor agonist (lacking selectivity) with K i values of 2.6 and 28 nM, respectively [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 333962-91-7. Pack Sizes: 5 mg. Product ID: HY-103170. | |
| LUF5834 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| LUF 5834 | LUF 5834. Group: Biochemicals. Grades: Purified. CAS No. 333962-91-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| LUF6283 | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| LUF 6283 | LUF 6283. Group: Biochemicals. Grades: Purified. CAS No. 92933-48-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| LUF7346 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lufenuron | Lufenuron. Group: Biochemicals. Alternative Names: N-[[[2, 5-Dichloro-4- (1, 1, 2, 3, 3, 3-hexafluoropropoxy) phenyl]amino]carbonyl]-2, 6-difluorobenzamide; (RS) -1-[2, 5-Dichloro-4- (1, 1, 2, 3, 3, 3-hexafluoropropoxy) phenyl]-3- (2, 6-difluorobenzoyl) urea; CGA 184699; Cigna; Fluphenacur; Fuoro; Lufenuron; Match; Match (pesticide); Match 5EC; Program. Grades: Highly Purified. CAS No. 103055-07-8. Pack Sizes: 250mg. Molecular Formula: C17H8Cl2F8N2O3, Molecular Weight: 511.15. US Biological Life Sciences. | Worldwide |
| Lufenuron | Lufenuron is a benzoylurea pesticide which inhibits the production of chitin in larval fleas. Synonyms: N-[[[2,5-Dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]amino]carbonyl]-2,6-difluorobenzamide; (RS)-1-[2,5-Dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea; CGA 184699; Cigna; Fluphenacur; Fuoro; Match; Match (pesticide); Match 5EC; Program. Grade: >95%. CAS No. 103055-07-8. Molecular formula: C17H8Cl2F8N2O3. Mole weight: 511.15. | |
| Lufenuron | Lufenuron is an orally active lipophilic benzoylurea insecticide and a chitin synthesis inhibitor that can used for flea and fish lice control. Lufenuron inhibits moulting of arthropods. Lufenuron induces reproductive toxicity, genotoxic effects and oxidative stresses in pregnant albino rats and their fetuses [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 103055-07-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-115584. | |
| Lufenuron Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lufenuron Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lufenuron Related Compound G | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lugdunin | Lugdunin is an antibiotic peptide. Lugdunin inhibits bacteria by dissipating their membrane potential. Lugdunin is active against Gram-positive bacteria, such as S. aureus , and reduces S. aureus skin and nasal colonization. Lugdunin induces LL-37 and CXCL8/MIP-2 in human keratinocytes and mouse skin [1]. Uses: Scientific research. Group: Peptides. CAS No. 1989698-37-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P4200. | |
| Lugol Solution, Laboratory Grade, 100 mL | Characteristic: Purple-yellow liquid. Notes: 10% potassium iodide, 5% iodine. Storage Code: Green; general chemical storage. Alternative Names: Lugol's iodine, iodine potassium-iodide. Grades: chem-grade laboratory. Product ID: 872793. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Lugol Solution, Laboratory Grade, 1 L | Characteristic: Purple-yellow liquid. Notes: 10% potassium iodide, 5% iodine. As of July 2, 2007, this is a DEA-regulated substance. Storage Code: Green; general chemical storage. Alternative Names: Lugol's iodine, iodine potassium-iodide. Grades: chem-grade laboratory. Product ID: 872797. -- SOLD FOR EDUCATIONAL USE ONLY -- | |
| Lugol Solution, Laboratory Grade, 500 mL | Characteristic: Purple-yellow liquid Notes: 10% potassium iodide, 5% iodine. As of July 2, 2007, this is a DEA-regulated substance. Storage Code: Green; general chemical storage. Alternative Names: Lugol's iodine, iodine potassium-iodide. Grades: chem-grade laboratory. Product ID: 872795. -- SOLD FOR EDUCATIONAL USE ONLY -- | |
| Luisol A | Shows weak cytotoxic activity against different tumor cell lines, also has antiparasitic activity. Group: Biochemicals. Alternative Names: (4R, 6S, 6aR, 7S, 12R, 12aS)-6a, 7, 8, 12-Tetrahydroxy-6-methyl-3, 4, 6, 6a, 7, 12-hexahydro-2H-4, 12a-methano-naphtho[2, 3-b][1, 5]dioxocin-2-one. Grades: Highly Purified. CAS No. 225110-59-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Luliconazole | Luliconazole is an azole antifungal drug. Its mechanism of action involves inhibition of ergosterol biosynthesis by inhibition of sterol 14α-demethylase. Group: Biochemicals. Alternative Names: [R-(E)]-α-[4-(2,4-Dichlorophenyl)-1,3-dithiolan-2-ylidene]-1H-imidazole-1-acetonitrile; Lulicon; NND 502. Grades: Highly Purified. CAS No. 187164-19-8. Pack Sizes: 500mg, 1g. Molecular Formula: C??H?Cl?N?S?, Molecular Weight: 354.28. US Biological Life Sciences. | Worldwide |
| Luliconazole | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Luliconazole | Luliconazole (NND 502) is a topical antifungal imidazole antibiotic with broad-spectrum and potent antifungal activity. Luliconazole can be used for the research of skin infection, including dermatophytosis, tinea corporis, tinea pedis et al [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NND 502. CAS No. 187164-19-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 250 mg. Product ID: HY-14283. | |
| Luliconazole Impurity 1 | Luliconazole Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 101530-21-6. Molecular formula: C14H9Cl2N3S2. Mole weight: 354.27. Catalog: APB101530216. | |
| Luliconazole Impurity 4 | Luliconazole Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 101529-76-4. Molecular formula: C14H9Cl2N3S2. Mole weight: 354.27. Catalog: APB101529764. | |
| Lulizumab | Lulizumab (Humanized Anti-CD28 Recombinant Antibody) is a selective CD28 blockade, Lulizumab prevents T cell activation by selectively targeting CD28 signaling [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Humanized Anti-CD28 Recombinant Antibody. CAS No. 2235419-62-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99302. | |
| Lumacaftor | Lumacaftor (VX-809; VRT 826809) is a CFTR modulator that corrects the folding and trafficking of CFTR protein. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VX-809; VRT 826809. CAS No. 936727-05-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13262. | |
| Lumasiran | Lumasiran (ALN-G01), a siRNA product, reduces hepatic oxalate production by targeting glycolate oxidase. By silencing the gene encoding glycolate oxidase, Lumasiran depletes glycolate oxidase and thereby inhibits the synthesis of oxalate, which is the toxic metabolite that is directly associated with the clinical manifestations of Primary hyperoxaluria type 1 (PH1)[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALN-G01. CAS No. 1834610-13-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132588. | |
| Lumasiran sodium | Lumasiran sodium, an investigational RNA interference (RNAi) therapeutic agent, reduces hepatic oxalate production by targeting glycolate oxidase. Lumasiran sodium reduces urinary oxalate excretion, the cause of progressive kidney failure in primary hyperoxaluria type 1 (PH1) [1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1834612-06-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132613. | |
| Lumateperone | Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator. Lumateperone has anticancer activity and can also be used for the study of schizophrenia and bipolar depression [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ITI-007. CAS No. 313368-91-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17637. | |
| Lumateperone Impurity 19 | Lumateperone Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1059630-08-8. Molecular formula: C14H17BrN2O2. Mole weight: 325.21. Catalog: APB1059630088. | |
| Lumateperone tosylate | Lumateperone (ITI-007) tosylate is a 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator. Lumateperone tosylate has anticancer activity and can also be used in studies of psychiatric disorders such as schizophrenia [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ITI-007 tosylate. CAS No. 1187020-80-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19733. | |
| Lumateperone Tosylate | The tosylate salt form of Lumateperone which is an highly effective antagonist of 5-HT2A receptor, could be used against insomnia. Alternative Names: lumateperone (Tosylate). ITI-007 tosylate. ITI 007. CAS No. 1187020-80-9. Product ID: API1187020809. Molecular formula: C31H36FN3O4S. Mole weight: 565.7. EINECS: 827-249-5. SMILES: CC1=CC=C(C=C1)S(=O)(=O)O.CN1CCN2C3CCN(CC3C4=C2C1=CC=C4)CCCC(=O)C5=CC=C(C=C5)F. Appearance: Powder. Category: Antipsychotic APIs. |  |
| Lumazine | Lumazine is a fluorescent pteridine. Synonyms: 2,4-Pteridinediol; 2,4(1H,3H)-Pteridinedione. Grade: >95% by HPLC. CAS No. 487-21-8. Molecular formula: C6H4N4O2. Mole weight: 164.12. | |
| Lumbokinase | Lumbokinase attenuates myocardial ischemia-reperfusion (I-R) injury through the activation of Sirt1 signaling, and thus enhances autophagic flux and reduces I-R-induced oxidative damage, inflammation and apoptosis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 556743-18-1. Pack Sizes: 1 g; 5 g; 10 g. Product ID: HY-E70008. | |
| Lumbrican | Lumbrican has antibacterial and antifungal activities. Lumbrican was found in Lumbricus rubellus [Humus earthworm]. Grade: >96% by HPLC. | |
| Lumbrokinase | Lumbrukinase extracted from earthworm alimentary canal.Lumbrukinasehas the functions of hydrolyzing fibrin directly as well as indirectly by activating plasminogen into plasmin.The product has evident anti-thrombus and thrombolytic effects. Lumbrokinase in the medical profession is known as the King of thrombolytic therapy, extraction in the earthworm. Apply to affected area after the rapid infiltration of silt to dissolve the clot resistance to vascular flow, varicose veins falling gradually. Applications: Functional food, health care products and pharmaceuticals. Group: Others. Purity: 5000-20000 u/mg. Appearance: Light yellow or grey. Source: Earthworm. Lumbrokinase; Pheretima. Cat No: EXTC-133. | |
| Lumefantrine | Lumefantrine is an active antimalarial molecule used in combination with Artemether as a first- and second-line antimalarial drug with oral activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benflumetol. CAS No. 82186-77-4. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0803. | |
| Lumefantrine | Inhibits hemozoin formation. Antimalarial. Group: Biochemicals. Alternative Names: (9Z)-. Grades: Highly Purified. CAS No. 82186-77-4. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Lumefantrine-d18 | Inhibits hemozoin formation. Antimalarial. Group: Biochemicals. Alternative Names: (9Z)-o-d18)methyl]-9H-fluorene-4-methanol; 2-(Dibutylamino-d18)-1-[2,7-dichloro-9-[1-(4-chlorophenyl)meth-(Z)-ylidene]-9H-fluoren-4-yl]ethanol; Benflumelol-d18; Benflumetol-d18; dl-Benflumelol-d18. Grades: Highly Purified. CAS No. 1185240-53-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Lumefantrine-[d18] | Lumefantrine-[d18] is the labelled analogue of Lumefantrine, which is an antimalarial drug. Synonyms: Lumefantrine D18; Benflumetol D18; (9Z)-2,7-Dichloro-9-[(4-chlorophenyl)methylene]-α-[(dibutylamino-d18)methyl]-9H-fluorene-4-methanol; 2-(Dibutylamino-d18)-1-[2,7-dichloro-9-[1-(4-chlorophenyl)meth-(Z)-ylidene]-9H-fluoren-4-yl]ethanol. Grade: 98% by HPLC; 98% atom D. CAS No. 1185240-53-2. Molecular formula: C30H14D18Cl3NO. Mole weight: 547.05. | |
| Lumefantrine-[d9] | Lumefantrine-[d9] is the labelled analogue of Lumefantrine, which Inhibits hemozoin formation, used as antimalarial. Synonyms: Lumefantrine D9. Grade: 98% by HPLC; 98% atom D. CAS No. 2477594-24-2. Molecular formula: C30H23D9Cl3NO. Mole weight: 538.00. | |
| Lumefantrine impurity 3 | Lumefantrine impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1331642-68-2. Molecular formula: C30H32Cl3NO. Mole weight: 528.94. Catalog: APB1331642682. | |
| Lumefantrine Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lumichrome | Lumichrome, a photodegradation product of Riboflavin, is an endogenous compound in humans. Lumichrome inhibits human lung cancer cell growth and induces apoptosis via a p53-dependent mechanism. Lumichrom is the inhibitor for AKT/β-catenin signaling pathway [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1086-80-2. Pack Sizes: 50 mg; 100 mg. Product ID: HY-115385. | |
| Lumichrome | Lumichrome. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 7,8-Dimethylbenzo[g]pteridine-2,4-diol. Product Category: Heterocyclic Organic Compound. CAS No. 1086-80-2. Molecular formula: C12H10N4O2. Mole weight: 242.23. Purity: 90%+. Product ID: ACM1086802. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lumichrome | Lumichrome is a derivative of Riboflavin (R415000), a vitamin with a key role in maintaining cellular function and health in human and animals. Group: Biochemicals. Alternative Names: 7, 8-Dimethylbenzo [g]pteridine-2, 4 (1H, 3H) -dione; 7, 8-Dimethylalloxazine; 7,8-Dimethylisoalloxazine; NSC 96911; Riboflavin lumichrome. Grades: Highly Purified. CAS No. 1086-80-2. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Lumiflavin | Lumiflavine is a structural analog of the water-soluble vitamin riboflavin that has been used to study the mechanism of uptake of riboflavin into intestinal epithelial (Caco-2) and human retinal pigment epithelial (hRPE) cells.1,2 It inhibits the uptake of radiolabeled riboflavin approximately 3-fold (at 25uM) and 30-fold (at 10uM) in Caco-2 cells and hRPE cells, respectively.1,2. Group: Biochemicals. Alternative Names: 7, 8, 10-Trimethylbenzo [g]pteridine-2, 4 (3H, 10H) -dione; 4-hydroxy-7, 8, 10-trimethylbenzo [g]pteridin-2 (10H) -one; Lumiflavine; 7, 8, 10-Tri methyl isoalloxazine. Grades: Highly Purified. CAS No. 1088-56-8. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C13H12N4O2, Molecular Weight: 256.26. US Biological Life Sciences. | Worldwide |
| Lumiflavin-3-acetic Acid | The acetic acid derivative of Lumiflavin used in photochemical induced dynamic nuclear polarization (photo-CIDNP) study of flavoproteins. Lumiflavin-3-acetic Acid is also used in the study riboflavin-binding protein interaction. Group: Biochemicals. Alternative Names: 4,10-Dihydro-7,8,10-trimethyl-2,4-dioxobenzo[g]pteridine-3(2H)-acetic Acid; 3- (Carboxymethyl) lumiflavin; Flavin I; N3-Carboxymethyl Lumiflavin. Grades: Highly Purified. CAS No. 20227-26-3. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Lumiflavin-3-acetic Acid Ethyl Ester | Lumiflavin derivative used in photochemical induced dynamic nuclear polarization (photo-CIDNP) study of flavoproteins. Lumiflavin-3-acetic Acid is also used in the study riboflavin-binding protein interaction. Group: Biochemicals. Alternative Names: 4,10-Dihydro-7,8,10-trimethyl-2,4-dioxo-benzo[g]pteridine-3(2H)-acetic Acid Ethyl Ester. Grades: Highly Purified. CAS No. 74178-39-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Lumiflavin 5-Oxide | Lumiflavin derivative. Group: Biochemicals. Alternative Names: 7,8,10-Trimethyl-benzo[g]pteridine-2,4(3H,10H)-dione 5-Oxide. Grades: Highly Purified. CAS No. 36995-93-4. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Lumiliximab | Lumiliximab (Anti-CD23 Recombinant Antibody) is an anti- CD23 monoclonal antibody that inhibits allergen-induced responses [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Gomiliximab; IDEC-152; ST-152. CAS No. 357613-86-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99303. | |
| Luminacin C1 | It is produced by the strain of Streptomyces sp. Mer-VD1207. It has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL), Luminacin D has the strongest activity. Molecular formula: C25H36O9. Mole weight: 480.55. | |
| Luminacin E1 | It is produced by the strain of Streptomyces sp. Mer-VD1207. It has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL), Luminacin D has the strongest activity. Molecular formula: C26H38O9. Mole weight: 494.57. | |
| Luminacin F | It is produced by the strain of Streptomyces sp. Mer-VD1207. It has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL), Luminacin D has the strongest activity. Molecular formula: C25H36O8. Mole weight: 464.55. | |
| Luminacin G1 | It is produced by the strain of Streptomyces sp. Mer-VD1207. It has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL), Luminacin D has the strongest activity. Molecular formula: C25H36O8. Mole weight: 464.55. | |
| Luminacin G2 | It is produced by the strain of Streptomyces sp. Mer-VD1207. It has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL), Luminacin D has the strongest activity. Molecular formula: C25H36O8. Mole weight: 464.55. | |
| Luminamicin | It is produced by the strain of Actinoplanes coloradoensis. It mainly inhibits the anaerobic bacteria, such as clostridium and clostridium, and has certain effects on haemophilus influenzae and Gonorrhoeae cuminella, but not against other aerobic bacteria. Synonyms: Coloradocin; 1,24-Methano-1H,9H,15H-furo(3',4':10,11)(1,7)dioxacyclotetradecino(4,3-e)pyrano(2,3-i)(4)benzoxecin-6,13,15,18(3ah)-tetrone,4,5,7a,8,16,17,20,20a,24,25,26,26a-dodecahydro-8,26-dihydroxy-22,25-dimethyl-5-methoxy-. CAS No. 99820-21-0. Molecular formula: C32H38O12. Mole weight: 614.64. | |
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