SCHEMBL471136

SCHEMBL471136

CC(C)(O)c1cccc(N)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.56
MAPK1 P28482 1/20 0.56
CYP3A4 P08684 3/20 0.48
CASP1 P29466 2/20 0.48
RECQL P46063 1/20 0.48
ALDH1A1 P00352 7/20 0.44
TDP1 Q9NUW8 2/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
CA7 P43166 1/20 0.44
CA9 Q16790 1/20 0.44
CA14 Q9ULX7 1/20 0.44
NOS1 P29475 1/20 0.41
KDM4E B2RXH2 2/20 0.40
ENPP2 Q13822 1/20 0.40
MAOA P21397 1/20 0.38
F2 P00734 2/20 0.38
PRSS1 P07477 2/20 0.38
PRSS2 P07478 2/20 0.38

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
SCHEMBL31263652 1.00 TSHR (0.56) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL8432403 0.86 TSHR (0.56) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL304190 0.83 ESR1 (0.50) MAPK1CYP3A4ALDH1A1CA2ESR1
SCHEMBL29374282 0.81 TSHR (0.60) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL111419 0.81 MAPK1 (0.60) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL29403060 0.81 MAPK1 (0.60) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL125232 0.81 TSHR (0.60) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL31476400 0.81 TSHR (0.60) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL14196693 0.81 TSHR (0.50) TSHRMAPK1CYP3A4CASP1RECQL
SCHEMBL29467505 0.81 TSHR (0.50) TSHRMAPK1CYP3A4CASP1RECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4739683-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS Janssen Pharmaceutica NV (BE) 2026-05-13 EP disclosed
EP-3985001-B1 PHARMACEUTICAL COMPOSITION FOR USE IN TREATING A CANCER SERVIER LAB (FR) 2026-04-29 EP disclosed
US-20250206730-A1 THIAZOLE DERIVATIVE COMPOUND AND USES THEREOF AUTOTELIC BIO INC. (KR) 2025-06-26 US disclosed
WO-2025063816-A1 COMPOSITION FOR TREATING UTERINE FIBROSIS COMPRISING THIAZOLE DERIVATIVE COMPOUND 오토텔릭바이오 주식회사 2025-03-27 WO disclosed
WO-2025063820-A1 COMPOSITION FOR TREATING PULMONARY FIBROSIS COMPRISING THIAZOLE DERIVATIVE COMPOUND 오토텔릭바이오 주식회사 2025-03-27 WO disclosed
WO-2025063819-A1 COMPOSITION FOR TREATING FIBROTIC DISEASE COMPRISING THIAZOLE DERIVATIVE COMPOUND 오토텔릭바이오 주식회사 2025-03-27 WO disclosed
EP-4522618-A1 TETRAHYDROPYRIDO[3,4-D]PYRIMIDINES COMPOUNDS AS HPK1 INHIBITORS Merck Patent GmbH (DE) 2025-03-19 EP disclosed
WO-2025054339-A1 TRIAZOLOPYRIDINE COMPOUNDS AS INHIBITORS OF KIT ARCUS BIOSCIENCES, INC. (US) 2025-03-13 WO disclosed
EP-4501928-A1 THIAZOLE DERIVATIVE COMPOUND AND USES THEREOF Autotelic Bio Inc. (KR) 2025-02-05 EP disclosed
WO-2025008059-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS JANSSEN PHARMACEUTICA NV (BE) 2025-01-09 WO disclosed
EP-2085220-A2 Resin composition for laser engraving, relief printing plate precursor for laser engraving, relief printing plate and method of producing the same FUJIFILM Corporation (JP) 2009-08-05 EP disclosed
US-20090191479-A1 RESIN COMPOSITION FOR LASER ENGRAVING, RELIEF PRINTING PLATE PRECURSOR FOR LASER ENGRAVING, RELIEF PRINTING PLATE AND METHOD OF PRODUCING THE SAME FUJIFILM CORPORATION (JP) 2009-07-30 US disclosed
US-20090155247-A1 Methods of Using Death Receptor Agonists and EGFR Inhibitors ASHKENAZI AVI J 2009-06-18 US disclosed
EP-1622912-B1 2-ALKYNYL-AND 2-ALKENYL-PYRAZOLO- [4,3-E ] -1,2,4-TRIAZOLO- [1,5-C] -PYRIMIDINE ADENOSINE A2A RECEPTOR ANTAGONISTS SCHERING CORP (US) 2009-05-27 EP disclosed
US-7390927-B2 Process for preparing 3-aminophenylacetylenes FUJILFILM CORPORATION (JP) 2008-06-24 US disclosed
EP-1856053-A1 CINNAMIDE AND HYDROCINNAMIDE DERIVATIVES WITH RAF-KINASE INHIBITORY ACTIVITY MILLENNIUM PHARMACEUTICALS, INC. (US) 2007-11-21 EP disclosed
US-20070020261-A1 Combination therapy of her expressing tumors GENENTECH, INC. 2007-01-25 US disclosed
WO-2006076706-A1 CINNAMIDE AND HYDROCINNAMIDE DERIVATIVES WITH RAF-KINASE INHIBITORY ACTIVITY MILLENNIUM PHARMACEUTICALS, INC. (US) 2006-07-20 WO disclosed
US-20060160803-A1 Cinnamide and hydrocinnamide derivatives with kinase inhibitory activity MILLENNIUM PHARMACEUTICALS, INC. (US) 2006-07-20 US disclosed
WO-2005103055-A1 PYRAZOLO-[4,3-e]-1,2,4-TRIAZOLO-[1,5-c]-PYRIMIDINE ADENOSINE A2A RECEPTOR ANTAGONISTS SCHERING CORPORATION (US) 2005-11-03 WO 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 (4 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-20090155247-A1 Methods of Using Death Receptor Agonists and EGFR Inhibitors EGFR, ERBB4, TNFRSF9 TSHR 369/4885MAPK1 2182/4885CYP3A4 1789/4885
US-20250206730-A1 THIAZOLE DERIVATIVE COMPOUND AND USES THEREOF TGFBR1, TGFBR2, ALK TSHR 214/4885MAPK1 699/4885CYP3A4 2172/4885
US-20060160803-A1 Cinnamide and hydrocinnamide derivatives with kinase inhibitory activity MAP3K21, HIPK4, MAP3K20 TSHR 4724/4885MAPK1 123/4885CYP3A4 3567/4885
US-20070020261-A1 Combination therapy of her expressing tumors ERBB2, EGFR, ERBB3 TSHR 403/4885MAPK1 2954/4885CYP3A4 4762/4885

“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.