SCHEMBL4555534

SCHEMBL4555534

COc1ccc(N(N)C(=O)c2ccc(Cl)cc2)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 2/20 0.60
TP53 P04637 3/20 0.55
SMN1; SMN2 Q16637 1/20 0.52
RAB9A P51151 2/20 0.51
NPC1 O15118 1/20 0.51
HSP90AA1 P07900 1/20 0.51
ALDH1A1 P00352 1/20 0.49
MAPT P10636 2/20 0.49
THRB P10828 1/20 0.49
CYP11B1 P15538 1/20 0.49
CYP11B2 P19099 1/20 0.49
MAOB P27338 2/20 0.49
PTGS2 P35354 2/20 0.49
MAOA P21397 1/20 0.49
KDM4E B2RXH2 1/20 0.49
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
PARP1 P09874 1/20 0.47
PARP10 Q53GL7 1/20 0.47
PARP2 Q9UGN5 1/20 0.47

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
Hydrochloric Acid SCHEMBL2695169 0.98 HPGD (0.58) HPGDTP53SMN1; SMN2RAB9ANPC1
Hydrochloric Acid SCHEMBL11841082 0.84 TP53 (0.58) HPGDTP53RAB9ANPC1ALDH1A1
Hydrochloric Acid SCHEMBL11834603 0.84 TP53 (0.58) HPGDTP53RAB9ANPC1ALDH1A1
SCHEMBL16671797 0.84 KDM4E (0.59) HPGDRAB9ANPC1HSP90AA1ALDH1A1
SCHEMBL7865528 0.84 KDM4E (0.69) HPGDSMN1; SMN2RAB9ANPC1ALDH1A1
Hydrochloric Acid SCHEMBL11836563 0.83 HPGD (0.48) HPGDTP53SMN1; SMN2RAB9ANPC1
Hydrochloric Acid SCHEMBL5801075 0.83 HPGD (0.48) HPGDTP53SMN1; SMN2RAB9ANPC1
Hydrochloric Acid SCHEMBL11845983 0.83 KDM4E (0.67) HPGDSMN1; SMN2RAB9ANPC1ALDH1A1
Hydrochloric Acid SCHEMBL5550609 0.83 KDM4E (0.58) HPGDRAB9ANPC1HSP90AA1ALDH1A1
SCHEMBL17213443 0.83 HPGD (0.62) HPGDTP53SMN1; SMN2RAB9ANPC1

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4606791-B1 IMPROVED PROCESS FOR THE PREPARATION OF INDOMETHACIN FIS FABBRICA ITALIANA SINTETICI SPA (IT) 2026-04-08 EP claimed
EP-4606791-A1 IMPROVED PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2025-08-27 EP claimed
US-20250263373-A1 PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2025-08-21 US claimed
EP-4606791-B1 IMPROVED PROCESS FOR THE PREPARATION OF INDOMETHACIN FIS FABBRICA ITALIANA SINTETICI SPA (IT) 2026-04-08 EP disclosed
EP-4606791-A1 IMPROVED PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2025-08-27 EP disclosed
EP-4606791-A1 IMPROVED PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2025-08-27 EP disclosed
CN-120518519-A Improved process for preparing indomethacin F.I.S.菲博利佳意大利合成面料股份公司 2025-08-22 CN disclosed
US-20250263373-A1 PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2025-08-21 US disclosed
US-20250263373-A1 PROCESS FOR THE PREPARATION OF INDOMETHACIN F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2025-08-21 US disclosed
US-20210198197-A1 METHOD FOR SYNTHESIZING INDOMETHACIN AND ANALOGUE THEREOF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) 2021-07-01 US disclosed
US-8168656-B2 Indoleacetic acid and indenacetic acid derivatives as therapeutic agents with reduced gastrointestinal toxicity VANDERBILT UNIVERSITY (US) 2012-05-01 US disclosed
US-20090118290-A1 Indoleacetic acid and indenacetic acid derivatives as therapeutic agents with reduced gastrointestinal toxicity VANDERBILT UNIVERSITY 2009-05-07 US disclosed
US-7491744-B2 Indoleacetic acid and indenacetic acid derivatives as therapeutic agents with reduced gastrointestinal toxicity VANDERBILT UNIVERSITY (US) 2009-02-17 US disclosed
CN-1141627-A Indole derivatives for the treatment of estrogen-related tumors and diseases MERRELL DOW PHARMA (US) 1997-01-29 CN disclosed
US-4165428-A ANALGESICS, ANTIINFLAMMATORY AGENTS, ANTIPYRETICS HISAMITSU PHARMACEUTICAL CO., INC. (JP) 1979-08-21 US disclosed
US-3962471-A Indolylacetylamino acid derivatives, process for their preparation, and pharmaceutical compositions SCHERING AKTIENGESELLSCHAFT (DT) 1976-06-08 US 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-20210198197-A1 METHOD FOR SYNTHESIZING INDOMETHACIN AND ANALOGUE THEREOF IDO1, IDO2, PTGIS HPGD 19/4885TP53 1515/4885SMN1; SMN2 4675/4885
US-20090118290-A1 Indoleacetic acid and indenacetic acid derivatives as therapeutic agents with reduced gastrointestinal toxicity AANAT, FABP2, SI HPGD 65/4885TP53 742/4885SMN1; SMN2 4227/4885
US-20250263373-A1 PROCESS FOR THE PREPARATION OF INDOMETHACIN ADH1C, ADH1A, F12 HPGD 173/4885TP53 4286/4885SMN1; SMN2 3677/4885

“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.