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| Product | Description | |
|---|---|---|
| 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 | Indole-d6 is the deuterium labeled Indole. Indole is an endogenous metabolite. Uses: Scientific research. Category: Signaling pathways. CAS No. 104959-27-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W001132S. |  |
| 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. Category: Signaling pathways. CAS No. 73509-20-3. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Category: Signaling pathways. Alternative Names: Indole-3-lactic acid. CAS No. 1821-52-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113099. | |
| Indolelactic acid-d5 | Indolelactic acid-d5 is the deuterium labeled Indolelactic acid. Indolelactic acid is a tryptophan (Trp) catabolite in Azotobacter vinelandii cultures. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Indole-3-lactic acid-d5. CAS No. 2470130-19-7. Pack Sizes: 1 mg. Product ID: HY-113099S. | |
| 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 | Indolicidin is a potent antimicrobial peptide purified from the cytoplasmic granules of bovine neutrophils. Uses: Scientific research. Category: Signaling pathways. CAS No. 140896-21-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0261. | |
| Indolicidin Peptide Derivative With P-->a Substitution | Indolicidin Peptide Derivative With P-->a Substitution has antibacterial activity. | |
| 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. | |
| 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. CAS No. 496-15-1. |  Pennsylvania PA |
| Indoline-2-carboxylic acid | Indoline-2-carboxylic acid. CAS No: 78348-24-0 | Sarchem Laboratories New Jersey NJ |
| Indoline-4-carboxylic acid | Indoline-4-carboxylic acid. Alternative Names: 2,3-Dihydro-1H-indole-4-carboxylic acid. CAS No. 175647-03-7. Purity: 98.0%+. Product ID: ACM175647037-1. Molecular formula: C9H9NO2. Mole weight: 163.17. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Indoline-5-carboxylic acid | Indoline-5-carboxylic acid. Alternative Names: 1H-Indole-5-carboxylicacid, 2,3-dihydro-;5-Indolinecarboxylicacid (8CI);2,3-Dihydro-1H-indole-5-carboxylic acid;5-Carboxyindoline. CAS No. 15861-30-0. Product ID: ACM15861300. Molecular formula: C9H9NO2. Mole weight: 163.17. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indoline-6-carbonitrile hydrochloride | Indoline-6-carbonitrile hydrochloride. Alternative Names: Indoline-6-carbonitrile HCl. CAS No. 15861-35-5. Purity: 98.0%+. Product ID: ACM15861355. Molecular formula: C9H9ClN2. Mole weight: 180.63. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indoline-7-carboxaldehyde | Indoline-7-carboxaldehyde. Alternative Names: 2,3-Dihydro-1H-indole-7-carbaldehyde. CAS No. 143262-21-9. Purity: 98.0%. Product ID: ACM143262219. Molecular formula: C9H9NO. Mole weight: 147.17. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indoline-7-carboxylic acid | Indoline-7-carboxylic acid. 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. CAS No. 15861-40-2. Purity: 98.0%+. Product ID: ACM15861402. Molecular formula: C9H9NO2. Mole weight: 163.17. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indoline-7-carboxylic acid methyl ester | Indoline-7-carboxylic acid methyl ester. Alternative Names: 112106-91-9, Methyl indoline-7-carboxylate, 1H-Indole-7-carboxylic acid, 2,3-dihydro-, methyl ester, ACMC-209v2e, SureCN10661545, AGN-PC-000BP0, CTK0D2660, MolPort-020-003-454, ACN-P001092, ANW-44532, ZINC26894119, AKOS006312265, Indoline-7-carboxylic acid methyl ester, AK-92476, A-4944, I04-5944, 1H-Indole-7-carboxylic acid,2,3-dihydro-,methyl ester. CAS No. 112106-91-9. Purity: 96%. Product ID: ACM112106919. Molecular formula: C10H11NO2. Mole weight: 177.199840 [g/mol]. IUPAC Name: methyl 2,3-dihydro-1H-indole-7-carboxylate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indoline impurity 10 | Indoline impurity 10. Uses: For analytical and research use. Molecular formula: C13H16N2. Mole weight: 200.29. Catalog: APB11137. |  |
| Indoline impurity 11 | Indoline impurity 11. Uses: For analytical and research use. CAS No. 421578-44-1. Molecular formula: C16H14BrN3OS2. Mole weight: 408.33. Catalog: APB421578441. | |
| Indoline impurity 12 | Indoline impurity 12. Uses: For analytical and research use. CAS No. 219655-02-4. Molecular formula: C18H16N2OS2. Mole weight: 340.46. Catalog: APB219655024. | |
| Indoline impurity 14 | Indoline impurity 14. Uses: For analytical and research use. CAS No. 1093086-32-8. Molecular formula: C9H9NO2. Mole weight: 163.18. Catalog: APB1093086328. | |
| Indoline impurity 15 | Indoline impurity 15. Uses: For analytical and research use. CAS No. 90196-41-1. Molecular formula: C8H6N2O3. Mole weight: 178.15. Catalog: APB90196411. | |
| Indoline impurity 1 (Epalrestat impurities) | Indoline impurity 1 (Epalrestat impurities). Uses: For analytical and research use. CAS No. 1408072-62-7. Molecular formula: C19H25NO2. Mole weight: 299.41. Catalog: APB1408072627. | |
| Indoline impurity 2 | Indoline impurity 2. Uses: For analytical and research use. Molecular formula: C18H23NO3. Mole weight: 301.39. Catalog: APB11135. | |
| Indoline impurity 3 | Indoline impurity 3. Uses: For analytical and research use. CAS No. 752184-07-9. Molecular formula: C13H15NO. Mole weight: 201.27. Catalog: APB752184079. | |
| Indoline impurity 4 | Indoline impurity 4. Uses: For analytical and research use. CAS No. 1365920-38-2. Molecular formula: C26H31NO2. Mole weight: 389.53. Catalog: APB1365920382. | |
| Indoline impurity 5 | Indoline impurity 5. Uses: For analytical and research use. Molecular formula: C24H25N3O5. Mole weight: 435.48. Catalog: APB11136. | |
| Indoline impurity 6 | Indoline impurity 6. Uses: For analytical and research use. CAS No. 2788-23-0. Molecular formula: C12H8N2O. Mole weight: 196.21. Catalog: APB2788230. | |
| Indoline impurity 7 | Indoline impurity 7. Uses: For analytical and research use. CAS No. 117782-96-4. Molecular formula: C8H6N2O. Mole weight: 146.15. Catalog: APB117782964. | |
| Indolizine-2-carboxylic acid methyl ester | Indolizine-2-carboxylic acid methyl ester. CAS No. 16959-62-9. Product ID: ACM16959629. Alfa Chemistry - ISO 9001:32057 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. | |
| Indolo[2,3-a]carbazole | Indolo[2,3-a]carbazole. 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: C18H12N2. Mole weight: 256.30. Purity: 95%+. |  |
| Indolo[3,2,1-jk]carbazole | Indolo[3,2,1-jk]carbazole. CAS No. 205-95-8. Molecular formula: C18H11N. Mole weight: 241.3g/mol. IUPAC Name: 1-azapentacyclo[10.6.1.02,7.08,19.013,18]nonadeca-2,4,6,8(19),9,11,13,15,17-nonaene. SMILES: C1=CC=C2C(=C1)C3=C4N2C5=CC=CC=C5C4=CC=C3. InChI: 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. | |
| Indolo[3,2-b]carbazole | Indolo[3,2-b]carbazole. Alternative Names: 5,11-Dihydroindolo[3,2-B]Carbazole. CAS No. 6336-32-9. Molecular formula: C18H10N2. Mole weight: 254.29. Purity: 95%+. IUPAC Name: 5,11-dihydroindolo[3,2-b]carbazole. SMILES: C1=CC=C2C(=C1)C3=CC4=C(C=C3N2)C5=CC=CC=C5N4. InChI: 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. | |
| 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 | 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 is NSAID with anti-inflammatory, analgesic, and antipyretic properties. It is a synthetic nonsteroidal indole derivative with anti-inflammatory activity and chemopreventive properties. Indomethacin inhibits the enzyme cyclooxygenase, thereby preventing cyclooxygenase-mediated DNA adduct formation by heterocyclic aromatic amines. This agent also may inhibit the expression of multidrug-resistant protein type 1, resulting in increased efficacies of some antineoplastic agents in treating multi-drug resistant tumors. In addition, indomethacin activates phosphatases that inhibit the migration and proliferation of cancer cells and downregulates survival, which may result in tumor cell apoptosis. CAS No. 53-86-1. Product ID: PI53861. Molecular formula: C19H16ClNO4. Mole weight: 357.8. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indomethacin | Indomethacin (Indometacin) is a potent, orally active COX1/2 inhibitor with IC50 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. Category: Induced disease models products. Alternative Names: Indometacin. CAS No. 53-86-1. Pack Sizes: 10 mM * 1 mL in DMSO; 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 Acyl-b-D-glucuronide | Indomethacin Acyl-b-D-glucuronide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 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 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 EP impurity C | Indomethacin EP impurity C. Uses: For analytical and research use. CAS No. 4018-82-0. Molecular formula: C14H12ClNO2. Mole weight: 261.71. Catalog: APB4018820. | |
| Indomethacin EP impurity D | Indomethacin EP impurity D. Uses: For analytical and research use. Molecular formula: C19H16ClNO4. Mole weight: 357.79. Catalog: APB11141. | |
| Indomethacin EP impurity E | Indomethacin EP impurity E. Uses: For analytical and research use. CAS No. 807614-94-4. Molecular formula: C19H16ClNO4. Mole weight: 357.79. Catalog: APB807614944. | |
| Indomethacin EP impurity F | Indomethacin EP impurity F. Uses: For analytical and research use. CAS No. 402849-27-8. Molecular formula: C21H16Cl2N2O3. Mole weight: 415.27. Catalog: APB402849278. | |
| Indomethacin EP impurity G | Indomethacin EP impurity G. Uses: For analytical and research use. CAS No. 402849-26-7. Molecular formula: C19H15Cl2NO4. Mole weight: 392.23. Catalog: APB402849267. | |
| Indomethacin EP impurity H | Indomethacin EP impurity H. Uses: For analytical and research use. CAS No. 1601-18-9. Molecular formula: C20H18ClNO4. Mole weight: 371.82. Catalog: APB1601189. | |
| Indomethacin EP impurity I | Indomethacin EP impurity I. Uses: For analytical and research use. CAS No. 16401-99-3. Molecular formula: C21H20ClNO4. Mole weight: 385.84. Catalog: APB16401993. | |
| Indomethacin EP impurity J | Indomethacin EP impurity J. Uses: For analytical and research use. CAS No. 402849-25-6. Molecular formula: C33H27N3O5. Mole weight: 616.5. Catalog: APB402849256. | |
| INDOMETHACIN ESTER, N-HEPTYL- | INDOMETHACIN ESTER, N-HEPTYL-. CAS No. 282728-47-6. Product ID: ACM282728476. Molecular formula: C26H30ClNO4. Mole weight: 455.97. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Indomethacin methylester | Indomethacin methylester (Compound 10; Indometacin methylester) is a potent and selective AKR1C3 inhibitor with an IC50 value of 5.67 μM. Indomethacin methylester is promising for research of postate cancer[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Indometacin methylester. CAS No. 1601-18-9. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg; 250 mg; 1 g. Product ID: HY-W024692. | |
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