SCHEMBL4364435

SCHEMBL4364435

CC=CC=C(C(=O)O)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1C1 Q04828 4/20 0.52
AKR1C2 P52895 3/20 0.45
AKR1C3 P42330 2/20 0.45
PTGS2 P35354 1/20 0.44
KMT2A Q03164 3/20 0.43
ALDH1A1 P00352 3/20 0.41
MEN1 O00255 2/20 0.41
TSHR P16473 3/20 0.41
TDP1 Q9NUW8 2/20 0.41
POLB P06746 1/20 0.41
CYP3A4 P08684 1/20 0.41
PARP1 P09874 1/20 0.41
MAPT P10636 1/20 0.41
CYP2C19 P33261 1/20 0.41
RECQL P46063 1/20 0.41
BLM P54132 1/20 0.41
PMP22 Q01453 1/20 0.41
HSD17B10 Q99714 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
CA12 O43570 1/20 0.39

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
SCHEMBL8343039 1.00 AKR1C1 (0.52) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL8215241 0.89 POLB (0.50) AKR1C1PTGS2KMT2AALDH1A1MEN1
SCHEMBL13456929 0.86 CES2 (0.47) AKR1C1AKR1C2AKR1C3KMT2AALDH1A1
SCHEMBL10425749 0.85 AKR1C1 (0.40) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL367696 0.81 AKR1C1 (0.61) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL1996918 0.81 AKR1C1 (0.61) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL2555171 0.81 AKR1C1 (0.61) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL14638944 0.80 AKR1C1 (0.52) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL28796389 0.80 AKR1C1 (0.52) AKR1C1AKR1C2AKR1C3PTGS2KMT2A
SCHEMBL14638943 0.80 AKR1C1 (0.52) AKR1C1AKR1C2AKR1C3PTGS2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4430037-B1 ISOXAZOLIDINES AS RIPK1 INHIBITORS AND USE THEREOF GENZYME CORP (US) 2025-10-29 EP disclosed
US-20250282782-A1 PYRAZOLOPYRAZINE COMPOUNDS AS SHP2 INHIBITORS GENZYME CORP (US) 2025-09-11 US disclosed
EP-4573090-A1 ISOXAZOLIDINES AS RIPK1 INHIBITORS AND USE THEREOF GENZYME CORPORATION (US) 2025-06-25 EP disclosed
US-20250122186-A1 ISOXAZOLIDINES AS RIPK1 INHIBITORS AND USE THEREOF GENZYME CORP (US) 2025-04-17 US disclosed
WO-2025049419-A1 PYRAZOLYL COMPOUNDS AS EMOPAMIL BINDING PROTEIN INHIBITORS GENZYME CORPORATION (US) 2025-03-06 WO disclosed
US-20250064809-A1 Inhibitors of Mutant RET Kinases for use in Treating Cancer STEMLINE THERAPEUTICS, INC. (US) 2025-02-27 US disclosed
US-20250011338-A1 Kinase Inhibitors and Uses Thereof DENALI THERAPEUTICS INC. (US) 2025-01-09 US disclosed
US-12180211-B2 Compounds, compositions and methods DENALI THERAPEUTICS INC. (US) 2024-12-31 US disclosed
US-12129263-B2 Kinase inhibitors and uses thereof DENALI THERAPEUTICS INC. (US) 2024-10-29 US disclosed
EP-4448526-A1 PYRAZOLOPYRAZINE COMPOUNDS AS SHP2 INHIBITORS GENZYME CORPORATION (US) 2024-10-23 EP disclosed
WO-2016094846-A1 INHIBITORS OF CELLULAR NECROSIS AND RELATED METHODS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2016-06-16 WO disclosed
US-20160087213-A1 ORGANIC ELECTRONIC ELEMENT COMPRISING FULLERENE DERIVATIVE LG CHEM, LTD. (KR) 2016-03-24 US disclosed
EP-2975663-A1 ORGANIC ELECTRONIC ELEMENT COMPRISING FULLERENE DERIVATIVE LG Chem, Ltd. (KR) 2016-01-20 EP disclosed
US-20150203879-A1 Methods and Microorganisms for the Biological Synthesis of (S) -2-amino-6-hydroxypimelate, Hexamethylenediamine and 6-aminocaproate LCY BIOSCIENCES INC. (CA) 2015-07-23 US disclosed
US-7491743-B2 Inhibitors of cellular necrosis PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2009-02-17 US disclosed
US-20050119260-A1 Inhibitors of cellular necrosis BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2005-06-02 US disclosed
US-5968360-A ADDING A NONTOXIC TERPENE COMPOUND TO CONTAMINATED SOIL TO INDUCE MICROBIAL COMETABOLISM OF CHLORINATED BIPHENYLS; IN SITU BIOREMEDIATION THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1999-10-19 US disclosed
EP-0032548-B1 PROCESS FOR PREPARING ARYL AND HETEROARYL HEXADIENOIC ACIDS Montedison S.p.A. (IT) 1983-06-22 EP disclosed
US-4355168-A Process for preparing aryl- or heteroarylhexadienoic acids MONTEDISON S.P.A. (IT) 1982-10-19 US disclosed
EP-0032548-A1 Process for preparing aryl and heteroaryl hexadienoic acids Montedison S.p.A. (IT) 1981-07-29 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 (7 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-12180211-B2 Compounds, compositions and methods BAX, CASP3, CASP8 AKR1C1 3249/4885AKR1C2 2920/4885AKR1C3 2224/4885
US-20250011338-A1 Kinase Inhibitors and Uses Thereof MAP3K20, MAP3K6, MAP3K19 AKR1C1 3937/4885AKR1C2 3795/4885AKR1C3 3908/4885
US-20050119260-A1 Inhibitors of cellular necrosis TNF, AIFM1, BAD AKR1C1 2436/4885AKR1C2 2420/4885AKR1C3 1880/4885
US-20250064809-A1 Inhibitors of Mutant RET Kinases for use in Treating Cancer RET, BRAF, HRAS AKR1C1 3754/4885AKR1C2 3557/4885AKR1C3 3957/4885
US-20250282782-A1 PYRAZOLOPYRAZINE COMPOUNDS AS SHP2 INHIBITORS PTPN5, PTPN2, PTPRJ AKR1C1 4680/4885AKR1C2 4561/4885AKR1C3 4681/4885
US-20250122186-A1 ISOXAZOLIDINES AS RIPK1 INHIBITORS AND USE THEREOF RIPK1, RIPK2, RIPK3 AKR1C1 4324/4885AKR1C2 4287/4885AKR1C3 4477/4885
US-12129263-B2 Kinase inhibitors and uses thereof MAP3K20, MAP3K6, MAP3K19 AKR1C1 3937/4885AKR1C2 3795/4885AKR1C3 3908/4885

“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.