SCHEMBL14061414

SCHEMBL14061414

O=C1NCc2ccccc2CN1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 1/20 0.56
CA9 Q16790 1/20 0.56
ALOX15 P16050 1/20 0.50
HSD17B10 Q99714 1/20 0.50
CYP1A2 P05177 1/20 0.43
PNMT P11086 1/20 0.42
CD44 P16070 1/20 0.42
MAOB P27338 1/20 0.42
PARP1 P09874 2/20 0.42
PDPK1 O15530 1/20 0.41
PARP10 Q53GL7 1/20 0.41
PARP11 Q9NR21 1/20 0.41
GAA P10253 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
TYRO3 Q06418 1/20 0.39
NTRK2 Q16620 1/20 0.39
CLK4 Q9HAZ1 1/20 0.39
DYRK1B Q9Y463 1/20 0.39
AHR P35869 1/20 0.39
PDK2 Q15119 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
SCHEMBL14581370 0.87 CA12 (0.68) CA12CA9ALOX15HSD17B10CYP1A2
SCHEMBL45104 0.79 HTR5A (0.53) CA12CA9ALOX15HSD17B10GAA
SCHEMBL89023 0.77 ALOX15 (0.56) CA12CA9ALOX15HSD17B10CYP1A2
SCHEMBL23615628 0.75 CA12 (0.70) CA12CA9PARP1PDPK1PARP10
SCHEMBL518841 0.75 CA12 (0.44) CA12CA9ALOX15HSD17B10CYP1A2
SCHEMBL29546699 0.75 CA12 (0.44) CA12CA9ALOX15HSD17B10CYP1A2
SCHEMBL2062062 0.75 NPC1 (0.52) CA12CA9ALOX15HSD17B10PNMT
SCHEMBL820510 0.74 PARP11 (0.59) CA12CA9CYP1A2PNMTCD44
SCHEMBL6629246 0.74 CA12 (0.47) CA12CA9ALOX15HSD17B10CYP1A2
SCHEMBL8558277 0.72 ALOX15 (0.50) CA12CA9ALOX15HSD17B10PNMT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-121752551-A Process for the preparation of 1, 5-dihydro-2, 4-benzodiazepine-3-one derivatives and intermediates thereof and process for the preparation thereof 江苏恩华药业股份有限公司 2026-03-27 CN disclosed
EP-4700019-A1 CRYSTAL FORM OF 1,5-DIHYDRO-2,4-BENZODIAZEPINE-3-ONE DERIVATIVE CITRATE, PREPARATION METHOD, AND USE THEREOF Jiangsu NHWA Pharmaceutical Co., Ltd (CN) 2026-02-25 EP disclosed
CN-121039114-A Crystal forms of 1, 5-dihydro-2, 4-benzodiazepine-3-one derivative citrate, preparation method and application thereof 江苏恩华药业股份有限公司 2025-11-28 CN disclosed
EP-4144725-B1 1,5-DIHYDRO-2,4-BENZODIAZEPINE-3-ONE DERIVATIVE AND APPLICATION THEREOF JIANGSU NHWA PHARMACEUTICAL CO LTD (CN) 2025-11-26 EP disclosed
EP-4144725-C0 1,5-DIHYDRO-2,4-BENZODIAZEPINE-3-ONE DERIVATIVE AND APPLICATION THEREOF JIANGSU NHWA PHARMACEUTICAL CO LTD (CN) 2025-11-26 EP disclosed
CN-116444484-B Salts of 1, 5-dihydro-2, 4-benzodiazepine-3-one derivatives and uses thereof 江苏恩华药业股份有限公司 2025-07-15 CN disclosed
WO-2025044768-A1 PREPARATION METHOD FOR 1,5-DIHYDRO-2,4-BENZODIAZEPINE-3-ONE DERIVATIVE, INTERMEDIATE THEREFOR, AND PREPARATION METHOD FOR INTERMEDIATE 江苏恩华药业股份有限公司 2025-03-06 WO disclosed
WO-2024217521-A1 CRYSTAL FORM OF 1,5-DIHYDRO-2,4-BENZODIAZEPINE-3-ONE DERIVATIVE CITRATE, PREPARATION METHOD, AND USE THEREOF 江苏恩华药业股份有限公司 2024-10-24 WO disclosed
CN-115667236-B 1, 5-Dihydro-2, 4-benzodiazepine-3-one derivative and application thereof 江苏恩华药业股份有限公司 2024-04-26 CN disclosed
CN-115667236-B 1, 5-Dihydro-2, 4-benzodiazepine-3-one derivative and application thereof 江苏恩华药业股份有限公司 2024-04-26 CN disclosed
US-9346795-B2 Substituted sulfonamides useful as antiapoptotic Bcl inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2016-05-24 US disclosed
US-9346795-B2 Substituted sulfonamides useful as antiapoptotic Bcl inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2016-05-24 US disclosed
US-9346795-B2 Substituted sulfonamides useful as antiapoptotic Bcl inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2016-05-24 US disclosed
EP-2714681-B1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2015-06-24 EP disclosed
EP-2714681-B1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2015-06-24 EP disclosed
US-20140135318-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-15 US disclosed
US-20140135318-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-15 US disclosed
US-20140135318-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-15 US disclosed
WO-2012162365-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2012-11-29 WO disclosed
WO-2012162365-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2012-11-29 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 (1 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-20140135318-A1 SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS BCL2, BAX, BCL2A1 CA12 2654/4885CA9 2692/4885ALOX15 3561/4885

“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.