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| Product | Description | |
|---|---|---|
| Indole 98+% (HPLC) | Indole 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 120-72-9. Pack Sizes: 25g, 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences. |  Worldwide |
| indoleacetaldoxime dehydratase | This enzyme belongs to the family of lyases, specifically the "catch-all" class of lyases that do not fit into any other sub-class. This enzyme participates in cyanoamino acid metabolism. Group: Enzymes. Synonyms: indoleacetaldoxime hydro-lyase; 3-indoleacetaldoxime hydro-lyase; indole-3-acetaldoxime hydro-lyase; indole-3-acetaldehyde-oxime hydro-lyase; (indol-3-yl)acetaldehyde-oxime hydro-lyase. Enzyme Commission Number: EC 4.99.1.6. CAS No. 9024-27-5. 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-5363; indoleacetaldoxime dehydratase; EC 4.99.1.6; 9024-27-5; indoleacetaldoxime hydro-lyase; 3-indoleacetaldoxime hydro-lyase; indole-3-acetaldoxime hydro-lyase; indole-3-acetaldehyde-oxime hydro-lyase; (indol-3-yl)acetaldehyde-oxime hydro-lyase. Cat No: EXWM-5363. |  |
| indoleacetate-lysine synthetase | This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). Group: Enzymes. Synonyms: indoleacetate:L-lysine ligase (ADP-forming). Enzyme Commission Number: EC 6.3.2.20. CAS No. 103537-15-1. 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-5740; indoleacetate-lysine synthetase; EC 6.3.2.20; 103537-15-1; indoleacetate:L-lysine ligase (ADP-forming). Cat No: EXWM-5740. | |
| Indoleacetic Acid | Indoleacetic Acid. Group: Biochemicals. Alternative Names: 1H-Indole-3-acetic Acid; (1H-Indol-3-yl)acetic Acid; 3-(Carboxymethyl)-1H-indole; 3-(Carboxymethyl)indole; 3-IAA; 3-Indolyl methyl carboxylic Acid; Bioenraiz; GAP; Heteroauxin; IAA; Noclosan; Rhizopin. Grades: Highly Purified. CAS No. 87-51-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Indole Acetic Acid-[d7] | Indole Acetic Acid-[d7]. Synonyms: Indole Acetic Acid D7. Grade: 98% atom D. CAS No. 1173020-21-7. Molecular formula: C10H2D7NO2. Mole weight: 182.23. |  |
| indoleacetylglucose-inositol O-acyltransferase | The position of acylation is indeterminate because of the ease of acyl transfer between hydroxy groups. Group: Enzymes. Synonyms: indole-3-acetyl-β-1-D-glucoside:myo-inositol indoleacetyltransferase; 1-O-(indol-3-ylacetyl)-β-D-glucose:myo-inositol indole-3-ylacetyltransferase. Enzyme Commission Number: EC 2.3.1.72. CAS No. 74082-57-8. 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-2252; indoleacetylglucose-inositol O-acyltransferase; EC 2.3.1.72; 74082-57-8; indole-3-acetyl-β-1-D-glucoside:myo-inositol indoleacetyltransferase; 1-O-(indol-3-ylacetyl)-β-D-glucose:myo-inositol indole-3-ylacetyltransferase. Cat No: EXWM-2252. | |
| indoleamine 2,3-dioxygenase | A protohemoprotein. Requires ascorbic acid and methylene blue for activity. This enzyme has broader substrate specificity than EC 1.13.11.11, tryptophan 2,3-dioxygenase. It is induced in response to pathological conditions and host-defense mechanisms and its distribution in mammals is not confined to the liver. While the enzyme is more active with D-tryptophan than L-tryptophan, its only known function to date is in the metabolism of L-tryptophan. Superoxide radicals can replace O2 as oxygen donor. Group: Enzymes. Synonyms: IDO (ambiguous); tryptophan pyrrolase (ambiguous); D-tryptophan:oxygen 2,3-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.52. CAS No. 9014-51-1. 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-0571; indoleamine 2,3-dioxygenase; EC 1.13.11.52; 9014-51-1; IDO (ambiguous); tryptophan pyrrolase (ambiguous); D-tryptophan:oxygen 2,3-oxidoreductase (decyclizing). Cat No: EXWM-0571. | |
| Indoleamine 2,3-dioxygenase 1 (199-207) | Indoleamine 2,3-dioxygenase 1 (199-207) is amino acids 199 to 207 fragment of Indoleamine 2,3-dioxygenase 1. IDO1 is a member of a unique class of mammalian haem dioxygenases that catalyse the oxidative catabolism of the least-abundant essential amino acid, L-Trp (L-tryptophan), along the kynurenine pathway. Synonyms: IDO1 (199-207). | |
| Indole-d6 | Labelled Indole (I577320). Can be used in perfumes and in the synthesis of tryptophan. Group: Biochemicals. Alternative Names: 1H-Indole-d6; 1-Azaindene-d6; 1-Benzazole-d6; 2,3-Benzopyrrole-d6; Benzo[b]pyrrole-d6; Ketole-d6; NSC 1964-d6. Grades: Highly Purified. CAS No. 104959-27-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Indole-d7 | Indole-d7 is the deuterium labeled Indole[1]. Indole is an endogenous metabolite. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 73509-20-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W001132S4. |  |
| Indole-[d7] | Indole-[d7]. Synonyms: Indole D7. Grade: 95% atom D. CAS No. 73509-20-3. Molecular formula: C8D7N. Mole weight: 124.19. | |
| Indole(Flavor grade) | Indole(Flavor grade). CAS No: 120-72-9 |  Sarchem Laboratories New Jersey NJ |
| indolelactate dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (indol-3-yl)lactate:NAD+ oxidoreductase. This enzyme is also called indolelactate:NAD+ oxidoreductase. This enzyme participates in tryptophan metabolism. Group: Enzymes. Synonyms: indolelactate:NAD+ oxidoreductase. Enzyme Commission Number: EC 1.1.1.110. CAS No. 37250-41-2. 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-0013; indolelactate dehydrogenase; EC 1.1.1.110; 37250-41-2; indolelactate:NAD+ oxidoreductase. Cat No: EXWM-0013. | |
| Indolelactic acid | Indolelactic acid (Indole-3-lactic acid) is a tryptophan (Trp) catabolite in Azotobacter vinelandii cultures. Indolelactic acid has anti-inflammation and potential anti-viral activity [1] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Indole-3-lactic acid. CAS No. 1821-52-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113099. | |
| Indolene 50% | Indolene 50% (Indole/Hydroxycitronellal Schiff Base). CAS No. REACTION MIXTURE. VIGON Item # 500896. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| indolepyruvate C-methyltransferase | The enzyme, characterized from the bacterium Streptomyces griseus, is involved in the biosynthesis of the antibacterial drug indolmycin. Group: Enzymes. Synonyms: ind1 (gene name); indolepyruvate methyltransferase; indolepyruvate 3-methyltransferase; indolepyruvic acid methyltransferase; S-adenosyl-L-methionine:indolepyruvate C-methyltransferase. Enzyme Commission Number: EC 2.1.1.47. CAS No. 54576-88-4. 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-1951; indolepyruvate C-methyltransferase; EC 2.1.1.47; 54576-88-4; ind1 (gene name); indolepyruvate methyltransferase; indolepyruvate 3-methyltransferase; indolepyruvic acid methyltransferase; S-adenosyl-L-methionine:indolepyruvate C-methyltransferase. Cat No: EXWM-1951. | |
| indolepyruvate decarboxylase | Thiamine diphosphate- and Mg2+-dependent. More specific than EC 4.1.1.1 pyruvate decarboxylase. Group: Enzymes. Synonyms: indol-3-yl-pyruvate carboxy-lyase; 3-(indol-3-yl)pyruvate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.74. CAS No. 9074-92-4. 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-4822; indolepyruvate decarboxylase; EC 4.1.1.74; 9074-92-4; indol-3-yl-pyruvate carboxy-lyase; 3-(indol-3-yl)pyruvate carboxy-lyase. Cat No: EXWM-4822. | |
| indolepyruvate ferredoxin oxidoreductase | Contains thiamine diphosphate and [4Fe-4S] clusters. Preferentially utilizes the transaminated forms of aromatic amino acids and can use phenylpyruvate and p-hydroxyphenylpyruvate as substrates. This enzyme, which is found in archaea, is a member of the 2-oxoacid oxidoreductases, a family of enzymes that oxidatively decarboxylate different 2-oxoacids to form their CoA derivatives, and are differentiated based on their substrate specificity. For examples of other members of this family, see EC 1.2.7.3, 2-oxoglutarate synthase and EC 1.2.7.7, 3-methyl-2-oxobutanoate dehydrogenase (ferredoxin). Group: Enzymes. Synonyms: 3-(indol-3-yl)pyruvate synthase (ferredoxin); IOR. Enzyme Commission Number: EC 1.2.7.8. CAS No. 158886-06-7. 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-1231; indolepyruvate ferredoxin oxidoreductase; EC 1.2.7.8; 158886-06-7; 3-(indol-3-yl)pyruvate synthase (ferredoxin); IOR. Cat No: EXWM-1231. | |
| Indolicidin | Indolicidin is the smallest of the naturally known occurring linear antimicrobial peptides, containing the highest percentage of tryptophan of any known protein, and consists of only six different amino acids. Indolicidin has been shown to be a fairly potent antimicrobial peptide with activity against a variety of microorganisms, fungi, and protozoa. Uses: Anti-infective agents. Synonyms: cationic antimicrobial peptide; H-Ile-Leu-Pro-Trp-Lys-Trp-Pro-Trp-Trp-Pro-Trp-Arg-Arg-NH2; L-isoleucyl-L-leucyl-L-prolyl-L-tryptophyl-L-lysyl-L-tryptophyl-L-prolyl-L-tryptophyl-L-tryptophyl-L-prolyl-L-tryptophyl-L-arginyl-L-argininamide. Grade: >98%. CAS No. 140896-21-5. Molecular formula: C100H132N26O13. Mole weight: 1906.28. | |
| Indolicidin Peptide Derivative With P-->a Substitution | Indolicidin Peptide Derivative With P-->a Substitution has antibacterial activity. | |
| Indolin-2-one | Indolin-2-one. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2H-Indol-2-one,1,3-dihydro-; 2-Indolinone(7CI,8CI); Oxindole (6CI); 1,3-Dihydro-2H-indol-2-one; 1,3-Dihydroindol-2-one; 2-Indolone; 2-Oxindole; 2-Oxo-2,3-dihydroindole; 2-Oxoindole; 2-Oxoindoline; Indol-2(3H)-one; NSC 274863; Oxindol. Product Category: Indoles. Appearance: Off-white crystalline powder. CAS No. 59-48-3. Molecular formula: C8H7NO. Mole weight: 133.15. Density: 1.327 g/cm³. Product ID: ACM59483. Alfa Chemistry ISO 9001:2015 Certified. Categories: Indolin-2-one monooxygenase. |  |
| indolin-2-one monooxygenase | The enzyme is involved in the biosynthesis of protective and allelophatic benzoxazinoids in some plants, most commonly from the family of Poaceae (grasses). It is a member of the cytochrome P-450 dependent monooxygenases. Group: Enzymes. Synonyms: BX3 (gene name); CYP71C2 (gene name). Enzyme Commission Number: EC 1.14.13.138. 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-0737; indolin-2-one monooxygenase; EC 1.14.13.138; BX3 (gene name); CYP71C2 (gene name). Cat No: EXWM-0737. | |
| Indolin-7-ol | Indolin-7-ol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 7-hydroxyindoline; 1H-Indol-7-ol, 2,3-dihydro-; 2,3-Dihydro-1H-indol-7-ol. Product Category: Indoles. Appearance: White crystal powder. CAS No. 4770-38-1. Molecular formula: C8H9NO. Mole weight: 135.16. Purity: 98.0%+. Product ID: ACM4770381. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline | Indoline. Uses: As an indole derivative, indoline can be used in the preparation of various medicinal compounds such as potential α1-adrenoceptor (α1-ar) antagonists. Additional or Alternative Names: AI3-39164; 15617-EP2311829A1; 2,3-dihydro-1 H-indole; aza-indane; 27157-EP2314575A1; Indoline, Vetec(TM) reagent grade, 98%; AC1Q1H8F; DTXSID9052133; 15617-EP2295429A1; 15617-EP2305648A1. Product Category: Indoles. CAS No. 496-15-1. Molecular formula: C8H9N. Mole weight: 119.167g/mol. IUPACName: 2,3-dihydro-1H-indole. Canonical SMILES: C1CNC2=CC=CC=C21. ECNumber: 207-816-8. Product ID: ACM496151. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline | An indole derivative used in the preparation of various medicinal compounds such as potential α1-adrenoceptor (α1-AR) antagonists. Group: Biochemicals. Alternative Names: 1-Azaindan; 1H-Indoline; 2,3-Dihydro-1H-indole; 2,3-Dihydroindole. Grades: Highly Purified. CAS No. 496-15-1. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Indoline | Indoline is a derivative of Indole (HY-W001132). Indoline can used as the basic structure for CD4 mimetic compounds (CD4mcs), which triggers conformational changes of the HIV-1 envelope glycoprotein (Env) in advance, and causes viral inactivation [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 496-15-1. Pack Sizes: 10 mM * 1 mL; 25 g; 100 g. Product ID: HY-Y0788. | |
| Indoline | Indoline. CAS No. 496-15-1. |  Pennsylvania PA |
| Indoline-2-carboxylic acid | Indoline-2-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Indoline-2-carboxylic. Product Category: Indoles. Appearance: Beige solid. CAS No. 78348-24-0. Molecular formula: C9H9NO2. Mole weight: 163.17. Purity: 0.97. IUPACName: 2,3-Dihydro-1H-indole-2-carboxylic acid. Canonical SMILES: C1C(NC2=CC=CC=C21)C(=O)O. Density: 1.286±0.06 g/cm³. Product ID: ACM78348240. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-2-carboxylic acid | Indoline-2-carboxylic acid. CAS No: 78348-24-0 | Sarchem Laboratories New Jersey NJ |
| Indoline-3-carboxylic acid | Indoline-3-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-DIHYDRO-1H-INDOLE-3-CARBOXYLIC ACID; 1H-INDOLINE-3-CARBOXYLIC ACID. Product Category: Indoles. CAS No. 39891-70-8. Molecular formula: C9H9NO2. Mole weight: 163.17. Purity: 0.98. Product ID: ACM39891708. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-4-carboxylic acid | Indoline-4-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-Dihydro-1H-indole-4-carboxylic acid. Product Category: Indoles. Appearance: White crystal powder. CAS No. 175647-03-7. Molecular formula: C9H9NO2. Mole weight: 163.17. Purity: 98.0%+. Product ID: ACM175647037-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-4-ol | Indoline-4-ol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-dihydro-1H-indol-4-ol; 1H-Indol-4-ol, 2,3-dihydro-. Product Category: Indoles. Appearance: White crystal powder. CAS No. 85926-99-4. Molecular formula: C8H9NO. Mole weight: 135.16. Purity: 98.0%+. Product ID: ACM85926994. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-5-carbonitrile | Indoline-5-carbonitrile. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-dihydro-1H-indole-5-carbonitrile;5-Indolinecarbonitrile;5-Cyanoindoline. Product Category: Indoles. Appearance: White crystal powder. CAS No. 15861-23-1. Molecular formula: C9H8N2. Mole weight: 144.17. Purity: 98.0%+. Product ID: ACM15861231. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-5-carboxylic acid | Indoline-5-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1H-Indole-5-carboxylicacid, 2,3-dihydro-;5-Indolinecarboxylicacid (8CI);2,3-Dihydro-1H-indole-5-carboxylic acid;5-Carboxyindoline. Product Category: Indoles. CAS No. 15861-30-0. Molecular formula: C9H9NO2. Mole weight: 163.17. Density: 1.284 g/cm³. Product ID: ACM15861300. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-6-carbonitrile hydrochloride | Indoline-6-carbonitrile hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Indoline-6-carbonitrile HCl. Product Category: Indoles. Appearance: White crystal powder. CAS No. 15861-35-5. Molecular formula: C9H9ClN2. Mole weight: 180.63. Purity: 98.0%+. Product ID: ACM15861355. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2,3-DIHYDRO-1H-INDOLE-6-CARBONITRILE HYDROCHLORIDE. | |
| Indoline-7-carboxaldehyde | Indoline-7-carboxaldehyde. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-Dihydro-1H-indole-7-carbaldehyde. Product Category: Indoles. Appearance: White crystal powder. CAS No. 143262-21-9. Molecular formula: C9H9NO. Mole weight: 147.17. Purity: 0.98. Product ID: ACM143262219. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline-7-carboxylic acid | Indoline-7-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3-dihydro-1h-indole-7-carboxylic acid; 1H-Indole-7-carboxylic acid, 2,3-dihydro-; 1h-indole-7-carboxylic acid,2,3-dihydro-; 7-Indolinecarboxylic Acid. Product Category: Indoles. Appearance: White crystal powder. CAS No. 15861-40-2. Molecular formula: C9H9NO2. Mole weight: 163.17. Purity: 98.0%+. Product ID: ACM15861402. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indoline impurity 1 (Epalrestat impurities) | Indoline impurity 1 (Epalrestat impurities). Uses: For analytical and research use. Group: Impurity standards. CAS No. 1408072-62-7. Molecular formula: C19H25NO2. Mole weight: 299.41. Catalog: APB1408072627. |  |
| Indolizine-2-carboxylic acid | Indolizine-2-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: INDOLIZINE-2-CARBOXYLIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 3189-48-8. Molecular formula: C9H7NO2. Mole weight: 161.1598. Purity: 0.96. Product ID: ACM3189488. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indolmycin | Indolmycin (TAK-083), an antibiotic, is a competitive inhibitor of prokaryotic tryptophanyl-tRNA synthetase (TrpS). Indolmycin (TAK-083) possesses both anti-viral and anti-bacterial activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-083; PA-155A. CAS No. 21200-24-8. Pack Sizes: 1 mg. Product ID: HY-117319. | |
| Indolmycin | Indolmycin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Indolmycin, 5-(1-(1H-Indol-3-yl)ethyl)-2-(methylamino)-4(5H)-oxazolone, AC1MIYC4, AGN-PC-037J1Q, CTK8G0314, 21200-24-8, AG-J-50905, 2-Oxazolin-4-one, 5-(1-indol-3-ylethyl)-2-(methylamino)-, 4(5H)-Oxazolone,5-(1-(1H-indol-3-yl)ethyl)-2-(methylamino)-, 5-[1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one, 21193-77-1. Product Category: Heterocyclic Organic Compound. CAS No. 21200-24-8. Molecular formula: C14H15N3O2. Mole weight: 257.287800 [g/mol]. Purity: 0.96. IUPACName: 5-[1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one. Canonical SMILES: CC(C1C(=O)N=C(O1)NC)C2=CNC3=CC=CC=C32. Product ID: ACM21200248. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indolmycin | A highly selective antibiotic which acts as a tryptophan anti-metabolite; active against mycobacteria and H. Pylori, and can stimulate transcription in escherichia coli. Synonyms: Indolemycin; PA 155 A; (-)-indolmycin; (1R,5S)-(-)-5-(1-Indol-3-ylethyl)-2-(methylamino)-2-oxazolin-4-one. Grade: >99% by HPLC (total diastereoisomers). CAS No. 21200-24-8. Molecular formula: C14H15N3O2. Mole weight: 257.29. | |
| Indolmycin (Antibiotic PA 155A) | Indolmycin is a highly selective antibiotic which acts as a tryptophan anti-metabolite. Recent research has shown that indolmycin is active against Mycobacteria and Helicobacter pylori and can stimulate transcription in Escherichia coli. Group: Biochemicals. Alternative Names: Antibiotic PA 155A. Grades: Highly Purified. CAS No. 21200-24-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Indolo[2,3-a]carbazole | Indolo[2,3-a]carbazole. Group: Organic light-emitting diode (oled) materials. Alternative Names: 11,12-DIHYRDOINDOLO[2,3-A]CARBAZOLE; INDOLO[2,3-A]CARBAZOLE; 11,12-Dihydroindolo[2,3-a]carbazole. CAS No. 60511-85-5. Molecular formula: 256.30. Mole weight: C18H12N2. 95%+. |  |
| Indolo[3,2,1-jk]carbazole | Indolo[3,2,1-jk]carbazole. Group: Small molecule semiconductor building blocks. CAS No. 205-95-8. Product ID: 1-azapentacyclo[10.6.1.02, 7.08, 19.013, 18]nonadeca-2, 4, 6, 8(19), 9, 11, 13, 15, 17-nonaene. Molecular formula: 241.3g/mol. Mole weight: C18H11N. C1=CC=C2C (=C1)C3=C4N2C5=CC=CC=C5C4=CC=C3. InChI=1S/C18H11N/c1-3-10-16-12 (6-1)14-8-5-9-15-13-7-2-4-11-17 (13)19 (16)18 (14)15/h1-11H. SZLNOBJKCVERBJ-UHFFFAOYSA-N. | |
| Indolo[3,2-b]carbazole | Indolo[3,2-b]carbazole. Group: Organic light-emitting diode (oled) materials. Alternative Names: 5,11-Dihydroindolo[3,2-B]Carbazole. CAS No. 6336-32-9. Product ID: 5,11-dihydroindolo[3,2-b]carbazole. Molecular formula: 254.29. Mole weight: C18H10N2. C1=CC=C2C (=C1)C3=CC4=C (C=C3N2)C5=CC=CC=C5N4. InChI=1S/C18H12N2/c1-3-7-15-11 (5-1)13-9-18-14 (10-17 (13)19-15)12-6-2-4-8-16 (12)20-18/h1-10, 19-20H. YCPBCVTUBBBNJJ-UHFFFAOYSA-N. 95%+. | |
| Indolyl-3-(ethyl-ß-bromide) (3-(2-Bromoethyl)-1H-Indole) | Indolyl-3-(ethyl-ß-bromide) (3-(2-Bromoethyl)-1H-Indole). Group: Biochemicals. Alternative Names: 3-(2-Bromoethyl)-1H-Indole. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| indolylacetylinositol arabinosyltransferase | The position of acylation is indeterminate because of the ease of acyl transfer between hydroxy groups. For a diagram showing the biosynthesis of UDP-L-arabinose, click here. Group: Enzymes. Synonyms: arabinosylindolylacetylinositol synthase; UDP-L-arabinose:indol-3-ylacetyl-myo-inositol L-arabinosyltransferase; UDP-L-arabinose:(indol-3-yl)acetyl-myo-inositol L-arabinosyltransferase. Enzyme Commission Number: EC 2.4.2.34. CAS No. 84720-96-7. 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-2662; indolylacetylinositol arabinosyltransferase; EC 2.4.2.34; 84720-96-7; arabinosylindolylacetylinositol synthase; UDP-L-arabinose:indol-3-ylacetyl-myo-inositol L-arabinosyltransferase; UDP-L-arabinose:(indol-3-yl)acetyl-myo-inositol L-arabinosyltransferase. Cat No: EXWM-2662. | |
| indolylacetyl-myo-inositol galactosyltransferase | This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. Group: Enzymes. Synonyms: uridine diphosphogalactose-indolylacetylinositol galactosyltransferase; indol-3-ylacetyl-myo-inositol galactoside synthase; UDP-galactose:indol-3-ylacetyl-myo-inositol 5-O-D-galactosyltransferase; UDP-galactose:(indol-3-yl)acetyl-myo-inositol 5-O-D-galactosyltransferase. Enzyme Commission Number: EC 2.4.1.156. CAS No. 85537-80-0. 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-2381; indolylacetyl-myo-inositol galactosyltransferase; EC 2.4.1.156; 85537-80-0; uridine diphosphogalactose-indolylacetylinositol galactosyltransferase; indol-3-ylacetyl-myo-inositol galactoside synthase; UDP-galactose:indol-3-ylacetyl-myo-inositol 5-O-D-galactosyltransferase; UDP-galactose:(indol-3-yl)acetyl-myo-inositol 5-O-D-galactosyltransferase. Cat No: EXWM-2381. | |
| Indomethacin | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Indomethacin | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C19H16ClNO4. CAS No. 53-86-1. Prepack ID 62725591-25g. Molecular Weight 357.79. See USA prepack pricing. |  |
| Indomethacin | Indomethacin (Indometacin) is a potent, orally active COX1/2 inhibitor with IC 50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin has anticancer activity and anti-infective activity. Indomethacin can be used for cancer, inflammation and viral infection research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Indometacin. CAS No. 53-86-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-14397. | |
| Indomethacin | Indomethacin. Group: Biochemicals. Grades: Purified. CAS No. 53-86-1. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Indomethacin | A nonselective COX1 and COX2 inhibitor with IC50 of 0.1 μg/mL and 5 μg/mL, respectively. Synonyms: indomethacin; 53-86-1; indometacin; Indocin; Indomethacine; Indometacine; Indocid; Reumacide; Indomethazine; Metindol; Artrinovo; Confortid; Idomethine; Indomecol; Indomethacinum; Metartril; Methazine; Artrivia; Dolovin; Imbrilon; Indacin; Indomed; Indomee; Indoptol; Infrocin; Metacen; Sadoreum; Amuno; Inacid; Tannex; Indo-rectolmin; Inteban sp; Artracin; Durametacin; Indoptic; Inflazon; Mikametan. Grade: 98%. CAS No. 53-86-1. Molecular formula: C18H18O2. Mole weight: 266.3. | |
| Indomethacin (1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic Acid) | Inhibits cyclooxygenase (IC50=0.1uM) selectively over liposygenases (IC50=100uM for 5-,12- and 15-LO). A clinically useful NAISD. Group: Biochemicals. Alternative Names: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic Acid. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Indomethacin, 2'-Trifluoromethyl (Indomethacin, 2'-Trifluoromethyl, Indomethacin, 2-CF3, CF3-Indomethacin, CF3-INDO) | A cell-permeable, bioavailable 2-trifluoromethyl analog of Indomethacin that acts as a highly potent, time-dependent inhibitor of cyclooxygenase -2 (COX-2; IC50=267 and 388nM for mouse and human COX-2, respectively) and its several mutant forms. Does not affect COX-1 activity even at high concentrations (IC50 >100uM). Interacts with human COX-2 with much greater affinity than indomethacin (KI = 1.5 vs 13uM) and blocks COX-2 dependent arachidonic acid oxygenation (IC50 = 150nM in 1483 human head and neck squamous cell carcinoma cells). Further, minimizes swelling in carrageenan-induced rat paw edema model (EC50 = 1.7mg/kg, p.o.) with no gastrointestinal bleeding at higher doses (10mg/kg). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Indomethacin Acyl-b-D-glucuronide | Indomethacin Acyl-b-D-glucuronide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Indomethacin - CAS 53-86-1 | A non-steroidal anti-inflammatory, cell permeable, antipyretic agent. Group: Fluorescence/luminescence spectroscopy. | |
| Indomethacin-[d4] | Indomethacin-[d4] is the labelled analogue of Indomethacin, which is a nonselective COX1 and COX2 inhibitor with IC50 of 0. 1 μg/mL and 5 μg/mL, respectively. Synonyms: Indomethacin D4; 1-(4-Chlorobenzoyl-d4)-5-methoxy-2-methyl-1H-indole-3-acetic Acid; Bonidon-d4; Catlep-d4; Indomethine-d4; Inacid-d4; Indomod-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 87377-08-0. Molecular formula: C19H12D4ClNO4. Mole weight: 361.81. | |
| Indomethacin-d4 (1-(4-Chlorobenzoyl-d4)-5-methoxy-2-methyl-1H-indole-3-acetic Acid, Indometacin-d4, Bonidon-d4, Catlep-d4, Indomethine-d4, Inacid-d4, Indomod-d4) | Nonsteroidal anti-inflammatory agent (NSAID). Group: Biochemicals. Alternative Names: 1-(4-Chlorobenzoyl-d4)-5-methoxy-2-methyl-1H-indole-3-acetic Acid; Indometacin-d4; Bonidon-d4; Catlep-d4; Indomethine-d4; Inacid-d4; Indomod-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Indomethacin-d4 Methyl Ester | Labeled selective COX-2 inhibitor. Group: Biochemicals. Alternative Names: 1-(4-(Chlorobenzoyl-d4))-5-methoxy-2-methyl-1H-indole-3-acetic Acid Methyl Ester; Methyl N-(p-Chlorobenzoyl-d4)-2-methyl-5-methoxy-3-indolylacetate; L 588983-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Indomethacin Diamide | Indomethacin Diamide. Group: Biochemicals. Alternative Names: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-Indole-3-acetic Acid 2- (4-chlorobenzoyl) -2- (4-methoxyphenyl) hydrazide. Grades: Highly Purified. CAS No. 402849-25-6. Pack Sizes: 10mg. Molecular Formula: C33H27Cl2N3O5, Molecular Weight: 616.49. US Biological Life Sciences. | Worldwide |
| Indomethacin heptyl ester | methyl acetate solution, ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Indomethacin Methyl Ester | Selective COX-2 inhibitor. Group: Biochemicals. Alternative Names: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic Acid Methyl Ester; Methyl N-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetate; L 588983. Grades: Highly Purified. CAS No. 1601-18-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Indomethacin Morpholinylamide | BML-190 is a selective cannabinoid CB2 receptor inverse agonist with Ki of 435 nM, with 50-fold selectivity over CB1 receptor. Synonyms: BML-190; BML 190; BML190; LM-4131; LM4131; LM 4131; IMMA; Indomethacin Morpholinylamide; 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1-[2-(4-morpholinyl)-2-oxoethyl]-1H-indole. Grade: >98%. CAS No. 2854-32-2. Molecular formula: C23H23ClN2O4. Mole weight: 426.89. | |
| Indomethacin Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Indomethacin Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Indomethacin sodium | Indomethacin (Indometacin) sodium is a potent, orally active COX1/2inhibitor with IC50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin sodium has anticancer activity and anti-infective activity. Indomethacin sodium can be used for cancer, inflammation and viral infection research. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1h-indole-3-aceticacisodiumsalt;1-(p-chlorobenzoyl)-5-methoxy-2-methyl-indole-3-aceticacisodiumsalt;osmosin;sodium1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1h-indole-3-acetate;sodiumindomethacin;INDOMETHACIN SODIUM;1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid sodium salt;IndoMetacine sodiuM. Product Category: Inhibitors. CAS No. 7681-54-1. Molecular formula: C19H15ClNNaO4. Mole weight: 379.77. Product ID: ACM7681541. Alfa Chemistry ISO 9001:2015 Certified. | |
| Indomethacin sodium hydrate | Indomethacin (Indometacin) sodium hydrateis a potent, orally active COX1/2 inhibitor with IC 50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin sodium hydrateis has anticancer activity and anti-infective activity. Indomethacin sodium hydrateis can be used for cancer, inflammation and viral infection research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Indometacin sodium hydrate. CAS No. 74252-25-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-14397A. | |
| Indomonocarbocyanine Pyridine Salt | Indomonocarbocyanine Pyridine Salt. Group: Biochemicals. Alternative Names: 2-[3-[1,3-Dihydro-3,3-dimethyl-1-(4-sulfobutyl)-2H-indol-2-ylidene]-1-propen-1-yl]-3,3-dimethyl-1-(4-sulfobutyl)-3H-indolium Inner Salt Pyridine Salt. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
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