Indomethacin

Indomethacin

SCHEMBL4300161

CC(C)Cc1ccc(C(C)C(=O)O)cc1.COc1ccc2c(c1)c(CC(=O)O)c(C)n2C(=O)c1ccc(Cl)cc1

nearest known ligand 0.74

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Indomethacin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 10/20 0.74
PTGS1 known ✓ P23219 4/20 0.74
AKR1C3 P42330 6/20 0.74
AKR1C2 P52895 5/20 0.74
PPARG P37231 3/20 0.74
AKR1C4 P17516 2/20 0.74
AKR1C1 Q04828 2/20 0.74
ABCB1 P08183 2/20 0.74
GLO1 Q04760 2/20 0.74
HIF1A Q16665 2/20 0.74
KDM4E B2RXH2 1/20 0.74
MEN1 O00255 1/20 0.74
PTGES O14684 1/20 0.74
ABCC3 O15438 1/20 0.74
ABCC4 O15439 1/20 0.74
ABCB11 O95342 1/20 0.74
MT-CO2 P00403 1/20 0.74
LMNA P02545 1/20 0.74
ALB P02768 1/20 0.74
CYP1A2 P05177 1/20 0.74

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Indomethacin SCHEMBL6827247 0.93 PTGS2 (0.63) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL8702320 0.92 PTGS2 (0.80) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL11570993 0.90 PTGS2 (0.79) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL356273 0.90 PTGS2 (0.79) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL10863701 0.88 PTGS2 (0.57) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL25313463 0.86 PTGS2 (0.92) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL3518614 0.86 PTGS2 (1.00) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL29353712 0.86 PTGS2 (1.00) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL9300 0.86 PTGS2 (1.00) PTGS2AKR1C3AKR1C2PTGS1PPARG
Indomethacin SCHEMBL29525957 0.86 PTGS2 (1.00) PTGS2AKR1C3AKR1C2PTGS1PPARG

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111359007-B Modified bacterial cellulose hydrogel dressing and preparation method thereof 瑞希(重庆)生物科技有限公司 2022-01-11 CN claimed
CN-111359007-A Modified bacterial cellulose hydrogel dressing and preparation method thereof 瑞希(重庆)生物科技有限公司 2020-07-03 CN claimed
EP-1829528-A2 Aggregate with increased deformability, comprising at least three amphipats, for improved transport through semi-permeable barriers and for the non-invasive drug application in vivo, especially through the skin IDEA AG (DE) 2007-09-05 EP claimed
EP-1829527-A2 Aggregate with increased deformability, comprising at least three amphipats, for improved transport through semi-permeable barriers and for the non-invasive drug application in vivo, especially through the skin IDEA AG (DE) 2007-09-05 EP claimed
EP-1815846-A2 Aggregate with increased deformability, comprising at least three amphipats, for improved transport through semi-permeable barriers and for the non-invasive drug application in vivo, especially through the skin IDEA AG (DE) 2007-08-08 EP claimed
EP-1815847-A2 Aggregate with increased deformability, comprising at least three amphipats, for improved transport through semi-permeable barriers and for the non-invasive drug application in vivo, especially through the skin IDEA AG (DE) 2007-08-08 EP claimed
EP-1551370-A1 AGGREGATE WITH INCREASED DEFORMABILITY, COMPRISING AT LEAST THREE AMPHIPATS, FOR IMPROVED TRANSPORT THROUGH SEMI-PERMEABLE BARRIERS AND FOR THE NON-INVASIVE DRUG APPLICATION IN VIVO, ESPECIALLY THROUGH THE SKIN IDEA AG (DE) 2005-07-13 EP claimed
WO-2004032900-A1 AGGREGATE WITH INCREASED DEFORMABILITY, COMPRISING AT LEAST THREE AMPHIPATS, FOR IMPROVED TRANSPORT THROUGH SEMI-PERMEABLE BARRIERS AND FOR THE NON-INVASIVE DRUG APPLICATION IN VIVO, ESPECIALLY THROUGH THE SKIN IDEA AG (DE) 2004-04-22 WO claimed
US-20040071767-A1 NSAID formulations, based on highly adaptable aggregates, for improved transport through barriers and topical drug delivery IDEA AG (DE) 2004-04-15 US claimed
EP-1272218-A2 A PHARMACEUTICAL COMPOSITION FOR TREATMENT OF ACUTE, CHRONIC PAIN AND/OR NEUROPATHIC PAIN AND MIGRAINES Pfizer Products Inc. (US) 2003-01-08 EP claimed
EP-1146879-A4 METHODS AND COMPOSITIONS FOR PREVENTION AND TREATMENT OF RESTENOSIS WITH NON-STEROIDAL ANTI-INFLAMMATORY DRUGS UNIV ROCKEFELLER (US) 2002-07-03 EP claimed
EP-1146879-A1 METHODS AND COMPOSITIONS FOR PREVENTION AND TREATMENT OF RESTENOSIS WITH NON-STEROIDAL ANTI-INFLAMMATORY DRUGS THE ROCKEFELLER UNIVERSITY (US) 2001-10-24 EP claimed
WO-2001076576-A2 A PHARMACEUTICAL COMPOSITION FOR TREATMENT OF ACUTE, CHRONIC PAIN AND/OR NEUROPATHIC PAIN AND MIGRAINES PFIZER PRODUCTS INC. (US) 2001-10-18 WO claimed
WO-2000033790-A2 METHODS AND COMPOSITIONS FOR PREVENTION AND TREATMENT OF ARTERIAL LESIONS WITH NON-STEROIDAL ANTI-INFLAMMATORY DRUGS THE ROCKEFELLER UNIVERSITY (US) 2000-06-15 WO claimed
WO-2000033848-A1 METHODS AND COMPOSITIONS FOR PREVENTION AND TREATMENT OF RESTENOSIS WITH NON-STEROIDAL ANTI-INFLAMMATORY DRUGS THE ROCKEFELLER UNIVERSITY (US) 2000-06-15 WO claimed
US-20230357200-A1 SMALL MOLECULE STIMULATORS OF STEROID RECEPTOR COACTIVATOR-3 AND METHODS OF THEIR USE AS CARDIOPROTECTIVE AND/OR VASCULAR REGENERATIVE AGENTS BAYLOR COLLEGE OF MEDICINE (US) 2023-11-09 US disclosed
US-11708350-B2 Small molecule stimulators of steroid receptor coactivator-3 and methods of their use as cardioprotective and/or vascular regenerative agents BAYLOR COLLEGE OF MEDICINE (US) 2023-07-25 US disclosed
US-4976949-A ACTIVE MATERIALS IN MICROSPHERES WITH CONTROLLED DENSITY AND DIAMETER FOR DELIVERY INTO INTESTINAL TRACT WITH MEALS THE UNIVERSITY OF MICHIGAN (US) 1990-12-11 US disclosed
US-4879274-A IMPROVED ABSORPTION KAO CORPORATION (JP) 1989-11-07 US disclosed
EP-0216303-A2 External medication Kao Corporation (JP) 1987-04-01 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040071767-A1 NSAID formulations, based on highly adaptable aggregates, for improved transport through barriers and topical drug delivery SLC43A1, TRPV2, TRPA1 PTGS2 34/4885PTGS1 32/4885AKR1C3 1530/4885
US-11708350-B2 Small molecule stimulators of steroid receptor coactivator-3 and methods of their use as cardioprotective and/or vascular regenerative agents NCOA3, FABP3, NCOA1 PTGS2 351/4885PTGS1 173/4885AKR1C3 3412/4885
US-20230357200-A1 SMALL MOLECULE STIMULATORS OF STEROID RECEPTOR COACTIVATOR-3 AND METHODS OF THEIR USE AS CARDIOPROTECTIVE AND/OR VASCULAR REGENERATIVE AGENTS NCOA3, FABP3, NCOA1 PTGS2 351/4885PTGS1 173/4885AKR1C3 3412/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.