SCHEMBL394617

SCHEMBL394617

CCc1cc(C#N)ccc1C(=O)O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
XDH P47989 1/20 0.46
SLC22A12 Q96S37 1/20 0.46
KDM4C Q9H3R0 2/20 0.44
MAP2K1 Q02750 1/20 0.43
CYP2A6 P11509 1/20 0.42
NOTUM Q6P988 1/20 0.42
GABRP O00591 1/20 0.41
GABRD O14764 1/20 0.41
GABRA1 P14867 1/20 0.41
GABRB1 P18505 1/20 0.41
GABRG2 P18507 1/20 0.41
GABRB3 P28472 1/20 0.41
GABRA5 P31644 1/20 0.41
GABRA3 P34903 1/20 0.41
GABRA2 P47869 1/20 0.41
GABRB2 P47870 1/20 0.41
GABRA4 P48169 1/20 0.41
GABRE P78334 1/20 0.41
GABRA6 Q16445 1/20 0.41
GABRG1 Q8N1C3 1/20 0.41

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
SCHEMBL11434090 0.88 XDH (0.43) XDHSLC22A12KDM4CMAP2K1NOTUM
SCHEMBL2435113 0.86 CYP2A6 (0.40) XDHSLC22A12KDM4CMAP2K1CYP2A6
SCHEMBL23480907 0.86 SLC22A12 (0.46) XDHSLC22A12KDM4CMAP2K1NOTUM
SCHEMBL29740345 0.84 CYP2A6 (0.41) XDHSLC22A12KDM4CMAP2K1CYP2A6
SCHEMBL31084678 0.84 XDH (0.45) XDHSLC22A12KDM4CMAP2K1NOTUM
SCHEMBL1169569 0.84 CYP2A6 (0.41) XDHSLC22A12KDM4CMAP2K1CYP2A6
SCHEMBL30400690 0.83 PPARA (0.50)
SCHEMBL6132151 0.82 GABRP (0.41) KDM4CGABRPGABRDGABRA1GABRB1
SCHEMBL10412862 0.82 GABRP (0.41) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL286231 0.81 CYP2A6 (0.43) MAP2K1CYP2A6MRGPRX4SETDB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114656373-B Cyano-substituted benzamide compound and application thereof 南通泰禾化工股份有限公司 2025-04-15 CN disclosed
CN-118005638-A Pyrazolo [3,4-d ] pyrimidine structure-containing compound, and preparation method and application thereof 西安新通药物研究股份有限公司 2024-05-10 CN disclosed
US-20230128402-A1 HETEROCYCLIC COMPOUNDS AND USES THEREOF THE TRUSTEES OF PRINCETON UNIVERSITY 2023-04-27 US disclosed
US-20230128402-A1 HETEROCYCLIC COMPOUNDS AND USES THEREOF THE TRUSTEES OF PRINCETON UNIVERSITY 2023-04-27 US disclosed
EP-4093400-A1 HETEROCYCLIC COMPOUNDS AND USES THEREOF The Trustees of Princeton University (US) 2022-11-30 EP disclosed
WO-2022135447-A1 CYANO-SUBSTITUTED BENZAMIDE COMPOUND AND APPLICATION THEREOF 南通泰禾化工股份有限公司 2022-06-30 WO disclosed
WO-2022135447-A1 CYANO-SUBSTITUTED BENZAMIDE COMPOUND AND APPLICATION THEREOF 南通泰禾化工股份有限公司 2022-06-30 WO disclosed
CN-114656373-A Cyano-substituted benzamide compound and application thereof 南通泰禾化工股份有限公司 2022-06-24 CN disclosed
WO-2021151062-A1 HETEROCYCLIC COMPOUNDS AND USES THEREOF THE TRUSTEES OF PRINCETON UNIVERISTY (US) 2021-07-29 WO disclosed
EP-3442958-B1 NOVEL N-[(PYRIDYLOXY)PROPANYL]BENZAMIDES BOEHRINGER INGELHEIM INT (DE) 2020-05-06 EP disclosed
US-20120088758-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2012-04-12 US disclosed
US-8101778-B2 Five-membered heterocycles useful as serine protease inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2012-01-24 US disclosed
US-20110319627-A1 METHODS OF SYNTHESIZING FACTOR Xa INHIBITORS MERCK SHARP & DOHME CORP. 2011-12-29 US disclosed
WO-2011084519-A1 METHODS OF SYNTHESIZING FACTOR XA INHIBITORS MILLENNIUM PHARMACEUTICALS, INC. (US) 2011-07-14 WO disclosed
CN-101414121-A Radiation sensitive composition for forming a colored layer, color filter and color liquid crystal display device JSR CORP (JP) 2009-04-22 CN disclosed
US-20090036438-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-05 US disclosed
US-7453002-B2 thrombotic or an inflammatory disorders; improved factor XIa and/or plasma kallikrein inhibitory activity and selectivity, dosage requirment, costs or feasibility, side effect reduction; 4-(aminomethyl)-N-[2-phenyl-1-(4-pyridin-2-yl-1H-imidazol-2-yl)ethyl]-trans-cyclohexanecarboxamide BRISTOL-MYERS SQUIBB COMPANY (US) 2008-11-18 US disclosed
EP-1773786-A2 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS Bristol-Myers Squibb Company (US) 2007-04-18 EP disclosed
WO-2005123050-A2 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-12-29 WO disclosed
US-20050282805-A1 thrombotic or an inflammatory disorders; improved factor XIa and/or plasma kallikrein inhibitory activity and selectivity, dosage requirment, costs or feasibility, side effect reduction; 4-(aminomethyl)-N-[2-phenyl-1-(4-pyridin-2-yl-1H-imidazol-2-yl)ethyl]-trans-cyclohexanecarboxamide BRISTOL-MYERS SQUIBB COMPANY 2005-12-22 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 (5 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-20120088758-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS F12, F11, F5 XDH 156/4885SLC22A12 4471/4885KDM4C 1128/4885
US-20110319627-A1 METHODS OF SYNTHESIZING FACTOR Xa INHIBITORS F12, F9, F7 XDH 39/4885SLC22A12 2713/4885KDM4C 1071/4885
US-20230128402-A1 HETEROCYCLIC COMPOUNDS AND USES THEREOF PAH, ALDH2, IDH2 XDH 292/4885SLC22A12 1576/4885KDM4C 1712/4885
US-20090036438-A1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS F12, F11, F5 XDH 156/4885SLC22A12 4471/4885KDM4C 1128/4885
US-20050282805-A1 thrombotic or an inflammatory disorders; improved factor XIa and/or plasma kallikrein inhibitory activity and selectivity, dosage requirment, costs or feasibility, side effect reduction; 4-(aminomethyl)-N-[2-phenyl-1-(4-pyridin-2-yl-1H-imidazol-2-yl)ethyl]-trans-cyclohexanecarboxamide F11, TFPI, F12 XDH 245/4885SLC22A12 3938/4885KDM4C 461/4885

“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.