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2,3-dihydroxyindole 2,3-dioxygenase This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O2. The systematic name of this enzyme class is 2,3-dihydroxyindole:oxygen 2,3-oxidoreductase (decyclizing). This enzyme participates in tryptophan metabolism. Group: Enzymes. Synonyms: 2,3-dihydroxyindole:oxygen 2,3-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.23. CAS No. 37256-62-5. 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-0542; 2,3-dihydroxyindole 2,3-dioxygenase; EC 1.13.11.23; 37256-62-5; 2,3-dihydroxyindole:oxygen 2,3-oxidoreductase (decyclizing). Cat No: EXWM-0542. Creative Enzymes
5,6-Dihydroxyindole 5,6-Dihydroxyindole, a melanin precursor, has a broad-spectrum antibacterial , antifungal , antiviral , antiparasitic activity. 5,6-Dihydroxyindole has cytotoxic effects and is strongly toxic against various pathogens [1]. Uses: Scientific research. Group: Natural products. CAS No. 3131-52-0. Pack Sizes: 100 mg; 1 g; 5 g. Product ID: HY-W018025. MedChemExpress MCE
5,6-Dihydroxyindole 5,6-Dihydroxyindole. Group: Biochemicals. Alternative Names: Dopamine lutine; Indole-5,6-diol. Grades: Highly Purified. CAS No. 3131-52-0. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. USBiological 7
Worldwide
5,6-Dihydroxyindole-2-carboxylic Acid 5,6-Dihydroxyindole-2-carboxylic Acid is the indole analogue of DOPA. 5,6-Dihydroxyindole-2-carboxylic Acid is a precursor to melanin as well as potential as HIV-1 integrase inhibitors. Group: Biochemicals. Alternative Names: 2-Carboxy-5,6-dihydroxyindole; 5,6-Dihydroxy-1H-indole-2-carboxylic Acid; 5,6-Dihydroxy-2-carboxyindole. Grades: Highly Purified. CAS No. 4790-8-3. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 2
Worldwide
5,6-dihydroxyindole-2-carboxylic acid oxidase (245-254) 5,6-dihydroxyindole-2-carboxylic acid oxidase (245-254) is a bioactive peptide of 5,6-dihydroxyindole-2-carboxylic acid oxidase. 5,6-dihydroxyindole-2-carboxylic acid oxidase takes a part in melanin biosynthesis and can regulate or influence the type of melanin synthesized. Synonyms: DHICA oxidase (245-254); Catalase B (245-254); Glycoprotein 75 (245-254); Melanoma antigen gp75 (245-254). BOC Sciences 9
5,6-dihydroxyindole-2-carboxylic acid oxidase (277-297) 5,6-dihydroxyindole-2-carboxylic acid oxidase (277-297) is a bioactive peptide of 5,6-dihydroxyindole-2-carboxylic acid oxidase. 5,6-dihydroxyindole-2-carboxylic acid oxidase takes a part in melanin biosynthesis and can regulate or influence the type of melanin synthesized. Synonyms: DHICA oxidase (277-297); Catalase B (277-297); Glycoprotein 75 (277-297); Melanoma antigen gp75 (277-297). BOC Sciences 9
5,6-dihydroxyindole-2-carboxylic acid oxidase (284-298) 5,6-dihydroxyindole-2-carboxylic acid oxidase (284-298) is a bioactive peptide of 5,6-dihydroxyindole-2-carboxylic acid oxidase. 5,6-dihydroxyindole-2-carboxylic acid oxidase takes a part in melanin biosynthesis and can regulate or influence the type of melanin synthesized. Synonyms: DHICA oxidase (284-298); Catalase B (284-298); Glycoprotein 75 (284-298); Melanoma antigen gp75 (284-298). BOC Sciences 9
5,6-dihydroxyindole-2-carboxylic acid oxidase (alt. ORF) 5,6-dihydroxyindole-2-carboxylic acid oxidase (alt. ORF) is a bioactive peptide of 5,6-dihydroxyindole-2-carboxylic acid oxidase. 5,6-dihydroxyindole-2-carboxylic acid oxidase takes a part in melanin biosynthesis and can regulate or influence the type of melanin synthesized. Synonyms: DHICA oxidase (alt. ORF); Catalase B (alt. ORF); Glycoprotein 75 (alt. ORF); Melanoma antigen gp75 (alt. ORF). BOC Sciences 9
5,6-Dihydroxyindole ≥97% 5,6-Dihydroxyindole ≥97%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. USBiological 4
Worldwide
DHICA DHICA (5,6-Dihydroxyindole-2-carboxylic acid) is an intermediate in melanin synthesis and a component of true black pigment, and its also a moderately potent GPR35 agonist. DHICA shows an ability to stimulate ?-arrestin translocation signaling with an EC50 value of 23.2 ?M in the U2OS cell line. DHICA plays a significant role in promoting and protecting against DNA damage[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5,6-Dihydroxyindole-2-carboxylic acid. CAS No. 4790-8-3. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-W018158. MedChemExpress MCE
DHICA DHICA is an intermediate in melanin synthesis and a component of true black pigment. DHICA is a moderately potent GPR35 agonist and shows an ability to stimulate β-arrestin translocation signaling with an EC50 value of 23.2 μM in the U2OS cell line. Synonyms: 5,6-dihydroxyindole-2-carboxylic acid; DHI2C; 5,6-Dhica. CAS No. 4790-8-3. Molecular formula: C9H7NO4. Mole weight: 193.16. BOC Sciences 7
L-dopachrome tautomerase (197-205) L-dopachrome tautomerase (197-205) is amino acids 197 to 205 fragment of L-dopachrome tautomerase. L-dopachrome tautomerase is involved in the pathway melanin biosynthesis, which is part of Pigment biosynthesis. It catalyzes the conversion of L-dopachrome into 5,6-dihydroxyindole-2-carboxylic acid (DHICA). Synonyms: DCT (197-205); L-dopachrome Delta-isomerase (197-205); TRP-2 (197-205). BOC Sciences 10
L-dopachrome tautomerase (241-250) L-dopachrome tautomerase (241-250) is amino acids 241 to 250 fragment of L-dopachrome tautomerase. L-dopachrome tautomerase is involved in the pathway melanin biosynthesis, which is part of Pigment biosynthesis. It catalyzes the conversion of L-dopachrome into 5,6-dihydroxyindole-2-carboxylic acid (DHICA). Synonyms: DCT (241-250); L-dopachrome Delta-isomerase (241-250); TRP-2 (241-250). BOC Sciences 10
L-dopachrome tautomerase (360-368) L-dopachrome tautomerase (360-368) is amino acids 360 to 368 fragment of L-dopachrome tautomerase. L-dopachrome tautomerase is involved in the pathway melanin biosynthesis, which is part of Pigment biosynthesis. It catalyzes the conversion of L-dopachrome into 5,6-dihydroxyindole-2-carboxylic acid (DHICA). Synonyms: DCT (360-368); L-dopachrome Delta-isomerase (360-368); TRP-2 (360-368). BOC Sciences 10
L-dopachrome tautomerase (387-395) L-dopachrome tautomerase (387-395) is amino acids 387 to 395 fragment of L-dopachrome tautomerase. L-dopachrome tautomerase is involved in the pathway melanin biosynthesis, which is part of Pigment biosynthesis. It catalyzes the conversion of L-dopachrome into 5,6-dihydroxyindole-2-carboxylic acid (DHICA). Synonyms: DCT (387-395); L-dopachrome Delta-isomerase (387-395); TRP-2 (387-395). BOC Sciences 10
L-dopachrome tautomerase (60-74) L-dopachrome tautomerase (60-74) is amino acids 60 to 74 fragment of L-dopachrome tautomerase. L-dopachrome tautomerase is involved in the pathway melanin biosynthesis, which is part of Pigment biosynthesis. It catalyzes the conversion of L-dopachrome into 5,6-dihydroxyindole-2-carboxylic acid (DHICA). Synonyms: DCT (60-74); L-dopachrome Delta-isomerase (60-74); TRP-2 (60-74). BOC Sciences 10
5,11-Dihydro-2,10-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde 5,11-Dihydro-2,10-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde. Group: Biochemicals. Grades: Highly Purified. CAS No. 549548-28-9. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C19H12N2O3. US Biological Life Sciences. USBiological 7
Worldwide
5,11-Dihydro-2,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde 5,11-Dihydro-2,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde. Group: Biochemicals. Grades: Highly Purified. CAS No. 549548-29-0. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C19H12N2O3. US Biological Life Sciences. USBiological 7
Worldwide
5,11-Dihydro-4,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde 5,11-Dihydro-4,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde. Group: Biochemicals. Grades: Highly Purified. CAS No. 549548-27-8. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C19H12N2O3. US Biological Life Sciences. USBiological 7
Worldwide
5,11-Dihydro-4,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde 5,11-Dihydro-4,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AGN-PC-0063M5, FT-0666935, 5,11-Dihydro-4,8-dihydroxyindolo[3,2-b]carbazole-6-carboxaldehyde, Indolo[3,2-b]carbazole-6-carboxaldehyde, 5,11-dihydro-4,8-dihydroxy-, 549548-27-8. Product Category: Heterocyclic Organic Compound. CAS No. 549548-27-8. Molecular formula: C19H12N2O3. Mole weight: 316.31. Purity: 0.96. IUPACName: 4,8-dihydroxy-5,11-dihydroindolo[3,2-b]carbazole-6-carbaldehyde. Canonical SMILES: C1=CC2=C(C(=C1)O)NC3=C(C4=C(C=C23)NC5=C4C=C(C=C5)O)C=O. Product ID: ACM549548278. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 4
5,6-Dihydroxyindoline 5,6-Dihydroxyindoline. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Indoline-5,6-diol hydrobromide; 5,6-Dihydroxyindoline hydrobromide. Appearance: White crystal powder. CAS No. 29539-03-5. Molecular formula: C8H10BrNO2. Mole weight: 232.07. Purity: 98.0%+. Product ID: ACM29539035. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
(-)-Lentiginosine (-)-Lentiginosine is a valuable compound used in the biomedical industry. With its potential anti-tumor and anti-inflammatory properties, this product proves effective in the treatment of various diseases. Research suggests that (-)-Lentiginosine exhibits cytotoxic activity against cancer cells, making it a promising candidate for drug development in cancer therapy. Synonyms: (1R,2R,8aR)-Octahydro-1,2-indolizinediol; (1R,2R,8aR)-1,2-Dihydroxyindolizidine; 1,2-Indolizinediol, octahydro-, [1R-(1α,2β,8aα)]-; (1R,2R,8aR)-Lentiginosine; Lentiginosine, (-)-. CAS No. 125279-72-3. Molecular formula: C8H15NO2. Mole weight: 157.21. BOC Sciences 2

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