SCHEMBL696050

SCHEMBL696050

OCc1cc(O)ccc1Cl

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.54
CA12 O43570 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
CA14 Q9ULX7 1/20 0.48
TTR P02766 1/20 0.41
TYR P14679 1/20 0.39
ESR1 P03372 5/20 0.39
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
MAPT P10636 1/20 0.38
ESR2 Q92731 3/20 0.38
CAMK2A Q9UQM7 1/20 0.38
CYP1A2 P05177 1/20 0.37
CYP3A4 P08684 1/20 0.37

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
SCHEMBL8738071 0.83 HSD17B10 (0.56) HSD17B10CA12CA1CA2CA7
SCHEMBL6131843 0.81 HSD17B10 (0.54) HSD17B10CA12CA1CA2CA7
SCHEMBL696223 0.81 HSD17B10 (0.54) HSD17B10CA12CA1CA2CA7
SCHEMBL11652162 0.79 HSD17B10 (0.52) HSD17B10CA12CA1CA2CA7
SCHEMBL12021260 0.79 HSD17B10 (0.52) HSD17B10CA12CA1CA2CA7
SCHEMBL23841643 0.79 HSD17B10 (0.52) HSD17B10CA12CA1CA2CA7
SCHEMBL365736 0.79 HSD17B10 (0.52) HSD17B10CA12CA1CA2CA7
SCHEMBL92968 0.78 CYP3A4 (0.48) HSD17B10MEN1KMT2AMAPTCYP1A2
SCHEMBL1605246 0.77 TYR (0.56) TYRMEN1KMT2AMAPTESR2
SCHEMBL31621229 0.76 RECQL (0.43) TTR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230054028-A1 PD-L1 ANTAGONIST COMPOUND ADLAI NORTYE BIOPHARMA CO., LTD. (CN) 2023-02-23 US disclosed
EP-4083032-A1 PD-L1 ANTAGONIST COMPOUND Adlai Nortye Biopharma Co., Ltd. (CN) 2022-11-02 EP disclosed
WO-2021129584-A1 PD-L1 ANTAGONIST COMPOUND 杭州阿诺生物医药科技有限公司 2021-07-01 WO disclosed
CN-104540826-B Spiro-fused piperidine derivatives useful as inhibitors of extrarenal potassium channels 默沙东公司 2018-04-20 CN disclosed
CN-104540826-A Spiro-fused piperidine derivatives useful as inhibitors of extrarenal potassium channels MERCK SHARP & DOHME 2015-04-22 CN disclosed
CN-102459216-B Inhibitors of renal outer medullary potassium channels MERCK SHARP & DO 2015-01-28 CN disclosed
US-8399436-B2 N-pyrazolyl carboxamides as CRAC channel inhibitors GLAXO GROUP LIMITED (GB) 2013-03-19 US disclosed
US-8399436-B2 N-pyrazolyl carboxamides as CRAC channel inhibitors GLAXO GROUP LIMITED (GB) 2013-03-19 US disclosed
US-8399436-B2 N-pyrazolyl carboxamides as CRAC channel inhibitors GLAXO GROUP LIMITED (GB) 2013-03-19 US disclosed
US-20120053150-A1 N-PYRAZOLYL CARBOXAMIDES AS CRAC CHANNEL INIHIBITORS GLAXO GROUP LIMITED (GB) 2012-03-01 US disclosed
US-20080312286-A1 Indanone Potentiators of Metabotropic Glutamate Receptors MERCK SHARP & DOHME CORP. 2008-12-18 US disclosed
EP-1778686-B1 TRIAZOLOPYRIDINYLSULFANYL DERIVATIVES AS P38 MAP KINASE INHIBITORS PFIZER LTD (GB) 2008-10-29 EP disclosed
CN-101006087-A Triazolopyridinylsulfanyl derivatives as p38 MAP kinase inhibitors PFIZER (US) 2007-07-25 CN disclosed
CN-1993335-A Indanone potentiators of metabotropic glutamate receptors MERCK & CO INC (US) 2007-07-04 CN disclosed
EP-1778686-A2 TRIAZOLOPYRIDINYLSULFANYL DERIVATIVES AS P38 MAP KINASE INHIBITORS Pfizer Limited (GB) 2007-05-02 EP disclosed
EP-1773792-A1 INDANONE POTENTIATORS OF METABOTROPIC GLUTAMATE RECEPTORS Merck & Co., Inc. (US) 2007-04-18 EP disclosed
WO-2006018718-A2 TRIAZOLOPYRIDINYLSULFANYL DERIVATIVES AS P38 MAP KINASE INHIBITORS PFIZER LIMITED (GB) 2006-02-23 WO disclosed
US-20060035922-A1 Triazolopyridinylsulfanyl derivatives as p38 MAP kinase inhibitors PFIZER INC. 2006-02-16 US disclosed
WO-2006015158-A1 INDANONE POTENTIATORS OF METABOTROPIC GLUTAMATE RECEPTORS MERCK & CO., INC. (US) 2006-02-09 WO disclosed
CN-1167670-C Aryl carboxylic acid and tetrazole derivant - 2004-09-22 CN 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-20060035922-A1 Triazolopyridinylsulfanyl derivatives as p38 MAP kinase inhibitors MAPK1, MAPKAPK5, MAPKAPK3 HSD17B10 3207/4885CA12 4629/4885CA1 3905/4885
US-20230054028-A1 PD-L1 ANTAGONIST COMPOUND CD274, PDCD1LG2, PDCD1 HSD17B10 2667/4885CA12 3762/4885CA1 4701/4885
US-20080312286-A1 Indanone Potentiators of Metabotropic Glutamate Receptors GRM2, GRIK2, GRM1 HSD17B10 1932/4885CA12 4562/4885CA1 2632/4885
US-20120053150-A1 N-PYRAZOLYL CARBOXAMIDES AS CRAC CHANNEL INIHIBITORS ORAI1, TRPV1, CACNA1E HSD17B10 3761/4885CA12 2179/4885CA1 1172/4885

“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.