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  1. General Info
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Drug Details
01. General Information
Name Indomethacin
PubChem CID 3715
Molecular Weight 357.8g/mol
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, Lausit, Mezolin, Mobilan, Indo-tablinen, Indo-Lemmon, Indometacinum, Indometacyna, Indometicina, Indocin Sr, Indometacina, Aconip, 2-(1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid, Indmethacine, Dolcidium, Elmetacin, Indomethine, Indorektal, Tivorbex, Catlep, Indoxen, Vonum, 1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, Indo-phlogont, Chibro-amuno, Bonidon Gel, Dolcidium PL, Rheumacin LA, Osmosin, 1-(p-Chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid, CCRIS 3502, HSDB 3101, Indometacine [INN-French], Indometacinum [INN-Latin], Indometacina [INN-Spanish], FLAM, Inteban, 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid, NCI-C56144, UNII-XXE1CET956, 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid, EINECS 200-186-5, XXE1CET956, MFCD00057095, Indometacin [INN], NSC-757061, 1-(p-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-acetic acid, BRN 0497341, USAN, Indomethacin (Indocid, Indocin), CHEBI:49662, CHEMBL6, NSC-77541, IMN, Indole-3-acetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-, Indomethacin [USAN:USP], alpha-(1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolyl)acetic acid, 2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl-1h-indol-3-yl}acetic acid, N-p-Chlorbenzoyl-5-methoxy-2-methylindole-3-acetic acid, MLS000069402, DTXSID9020740, (1-p-Chlorobenzoyl-5-methoxy-2-methylindol-3-yl)acetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indolylacetic acid, 1-(p-Chlorobenzoyl)-2-methoxy-3-methyl-1H-indole-3-acetic Acid, Indomet 140, EC 200-186-5, [1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetic acid, 5-22-05-00239 (Beilstein Handbook Reference), {1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl-1H-indol-3-yl}acetic acid, NSC 757061, CAS-53-86-1, 1-p-Cloro-benzoil-5-metoxi-2-metilindol-3-acido acetico, NCGC00015562-18, Indomethancin, 1-(4-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid, Arthrexin, Bonidin, Bonidon, Indameth, Indomod, Miametan, SMR000058195, Indomo, Flexin continus, Hicin, Kwas 1-(p-chlorobenzoilo)-2-metylo-5-metoksy-3-indolilooctowy, Chrono-indicid, Chrono-indocid, Indometacyna [Polish], Indometicina [Spanish], 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetic acid, Indo-Spray, Indomethacin (USAN:USP), Indolar SR, Indometacine (INN-French), Indometacinum (INN-Latin), Indometacina (INN-Spanish), INDOMETACIN (MART.), INDOMETACIN [MART.], DTXCID50740, INDOMETHACIN (USP-RS), INDOMETHACIN [USP-RS], 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indoleacetic acid, INDOMETACIN (EP MONOGRAPH), INDOMETACIN [EP MONOGRAPH], INDOMETHACIN (USP MONOGRAPH), INDOMETHACIN [USP MONOGRAPH], 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetic acid, (1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOL-3-YL)ACETIC ACID, 2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methylindol-3-yl}acetic acid, Indocin-SR, Indochron E-R, Indocin (TN), ACEMETACIN IMPURITY B (EP IMPURITY), ACEMETACIN IMPURITY B [EP IMPURITY], Aconip (TN), Indomethacin (USP), NSC77541, Indocid (pharmaceutical), SR-01000000014, Indomethacin & MAP-30, Indocollyre, Indonol, Innamit, 1-(p-Chlorobenzoyl)-5-methoxy-2-methyl-Indole-3-acetic acid, IndomethacinER, Indomethacin ER, 2-{1-((4-chlorophenyl)carbonyl)-5-methoxy-2-methylindol-3-yl}acetic acid, 4kyk, (1-((4-chlorophenyl)carbonyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid, Indomethacin,(S), Prestwick_597, INDREN, Indometacinum (Latin), Opera_ID_56, Spectrum_000919, Tocris-1708, 1z9h, 1-(p-Chlorbenzoyl)-5-methoxy-2-methylindol-3-essigsaeure [German], 1-p-Cloro-benzoil-5-metoxi-2-metilindol-3-acido acetico [Spanish], Prestwick0_000272, Prestwick1_000272, Prestwick2_000272, Prestwick3_000272, Spectrum2_000970, Spectrum3_000468, Spectrum4_000018, Spectrum5_000868, INDOMETACIN [JAN], INDOMETHACIN [MI], Lopac-I-7378, Kwas 1-(p-chlorobenzoilo)-2-metylo-5-metoksy-3-indolilooctowy [Polish], CHRONO-INDOCID 75, MolMap_000032, UPCMLD-DP023, I 7378, Indometacin (JP17/INN), INDOMETHACIN [HSDB], INDOMETHACIN [USAN], SCHEMBL9300, INDOMETHACIN [VANDF], Indomethacin Extended-release, Lopac0_000692, Oprea1_686105, BSPBio_000144, BSPBio_001149, BSPBio_002176, INDOMETACIN [WHO-DD], INDOMETACIN [WHO-IP], Indomethacine impurity mixture, KBioGR_000395, KBioGR_000489, KBioSS_000489, KBioSS_001399, MLS001074194, MLS006011845, BIDD:GT0132, DivK1c_000271, SPECTRUM1500350, SPBio_000979, SPBio_002363, BPBio1_000160, GTPL1909, Indomethacin, >=99% (TLC), UPCMLD-DP023:001, BDBM17638, CGIGDMFJXJATDK-UHFFFAOYSA-, HMS500N13, KBio1_000271, KBio2_000489, KBio2_001399, KBio2_003057, KBio2_003967, KBio2_005625, KBio2_006535, KBio3_000897, KBio3_000898, KBio3_001396, 1-(p-Chlorbenzoyl)-5-methoxy-2-methylindol-3-essigsaeure, C01EB03, M01AB01, M02AA23, S01BC01, Indomethacin - CAS 53-86-1, NINDS_000271, Bio2_000405, Bio2_000885, HMS1362I11, HMS1568H06, HMS1792I11, HMS1920F21, HMS1990I11, HMS2089N19, HMS2091N09, HMS2095H06, HMS2231J10, HMS3262K05, HMS3268A14, HMS3374F07, HMS3403I11, HMS3414N13, HMS3430L03, HMS3649K17, HMS3655O04, HMS3678N11, HMS3712H06, HMS3747K21, HMS3884E08, INDOMETHACIN [ORANGE BOOK], Indomethacin-d4(chlorobenzoyl-d4), Pharmakon1600-01500350, BCP18951, Indomethacin, >=99.0% (TLC), Tox21_113109, Tox21_201791, Tox21_300266, Tox21_500692, AC-532, CCG-40186, HB4422, INDOMETACINUM [WHO-IP LATIN], NSC757061, s1723, STL257874, AKOS000592893, Tox21_113109_1, AT13679, DB00328, Indometacin 1.0 mg/ml in Acetonitrile, KS-5255, LP00692, SDCCGSBI-0050670.P005, IDI1_000271, IDI1_002160, NCGC00015562-01, NCGC00015562-02, NCGC00015562-03, NCGC00015562-04, NCGC00015562-05, NCGC00015562-06, NCGC00015562-07, NCGC00015562-08, NCGC00015562-09, NCGC00015562-10, NCGC00015562-11, NCGC00015562-12, NCGC00015562-13, NCGC00015562-14, NCGC00015562-15, NCGC00015562-16, NCGC00015562-17, NCGC00015562-19, NCGC00015562-20, NCGC00015562-21, NCGC00015562-22, NCGC00015562-24, NCGC00015562-25, NCGC00015562-40, NCGC00024135-02, NCGC00024135-04, NCGC00024135-05, NCGC00024135-06, NCGC00024135-07, NCGC00024135-08, NCGC00024135-09, NCGC00024135-10, NCGC00024135-11, NCGC00024135-12, NCGC00024135-13, NCGC00024135-14, NCGC00024135-15, NCGC00254075-01, NCGC00259340-01, NCGC00261377-01, BI166166, BP-30207, HY-14397, NCI60_041708, O-Desmethyl-des-4-chlorobenzoylacemetacin, SBI-0050670.P004, DB-052413, AB00052022, EU-0100692, FT-0603227, I0655, NS00000217, SW196768-5, EN300-16807, Indomethacin, meets USP testing specifications, BIM-0050670.0001, C01926, D00141, S00108, AB00052022-20, AB00052022-21, AB00052022_23, AB00052022_24, L000959, Q409231, Indomethacin, Antibiotic for Culture Media Use Only, Q-201239, SR-01000000014-2, SR-01000000014-4, SR-01000000014-6, 1-(4-Chlorobenzoyl)-5-methoxy-2-met hyl-1H-indole, BRD-K57222227-001-06-1, BRD-K57222227-001-18-6, BRD-K57222227-001-27-7, SR-01000000014-10, SR-01000000014-16, Z56784896, 1-p-chlorobenzoyl-2-methyl-5-methoxyindol-3-acetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid, 1-(p-Chlorobenzoyl)-5-methoxy-2-methylindol-3-acetic acid, 1-(p-chlorobenzyl)-5-methoxy-2-methylindole-3-acetic acid, 1-(4-chloro-benzoyl)-5-methoxy-2-methyl-3-indolyl-acetic acid, 1-(4-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-acetic acid, 1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indole-acetic acid, 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indol acetic acid, Indomethacin, European Pharmacopoeia (EP) Reference Standard, N-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1-H-indole-3-acetic acid, Indomethacin, United States Pharmacopeia (USP) Reference Standard, N-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID, .alpha.-(1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolyl)acetic acid, [1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetic acid #, 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid & MAP-30, 1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl- (9CI), 2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2 methylindol-3-yl}acetic acid, 2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2methylindol-3-yl}acetic acid, Indole-3-acetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl- (8CI), Indomethacin, Pharmaceutical Secondary Standard; Certified Reference Material, InChI=1/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23)

Drug Type Small molecule
Formula C₁₉H₁₆ClNO₄
SMILES CC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)O
InChI 1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23)
InChIKey CGIGDMFJXJATDK-UHFFFAOYSA-N
CAS Number 53-86-1
ChEMBL ID CHEMBL6
ChEBI ID CHEBI:49662
TTD ID D0R1RS
Drug Bank ID DB00328
KEGG ID C01926
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 311
Pair Name Juglone, Indomethacin
Partner Name Juglone
Disease Info [ICD-11: 2B90] Colon cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Up-regulation Expression BAD hsa572
Up-regulation Expression BAX hsa581
Up-regulation Expression BBC3 hsa27113
Down-regulation Expression BCL2 hsa596
Up-regulation Expression CYCS hsa54205
Down-regulation Expression NFKB1 hsa4790
Down-regulation Expression PTGS2 hsa5743
Down-regulation Expression TNF hsa7124
In Vitro Model HT-29 Colon adenocarcinoma Homo sapiens (Human) CVCL_0320
Result A combination of both was shown to be more effective, suggesting that juglone may be considered for therapeutic intervention of colon cancer.
Decreasing Drug Toxicity
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Combination Pair ID: 313
Pair Name Juglone, Indomethacin
Partner Name Juglone
Disease Info [ICD-11: 2B90] Colon cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Up-regulation Expression BAD hsa572
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Expression CASP3 hsa836
Down-regulation Expression NFKB1 hsa4790
Down-regulation Expression PTGS2 hsa5743
Down-regulation Expression TNF hsa7124
In Vivo Model Adult male Balb/c mice were used in this study.
Result IND and JUG reduce the inflammatory activity and induce apoptotic cell death, while JUG effectively prevents IND induced gastric ulceration. These findings establish that a combination of IND + JUG may serve as a promising treatment regimen for colon cancer.
03. Reference
No. Title Href
1 Effects of combined treatment with Indomethacin and Juglone on AOM/DSS induced colon carcinogenesis in Balb/c mice: Roles of inflammation and apoptosis. Life Sci. 2021 Jan 1;264:118657. doi: 10.1016/j.lfs.2020.118657. Click
2 Indomethacin and juglone inhibit inflammatory molecules to induce apoptosis in colon cancer cells. J Biochem Mol Toxicol. 2020 Feb;34(2):e22433. doi: 10.1002/jbt.22433. Click
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