SCHEMBL2492354

SCHEMBL2492354

O/N=C/c1ccc(-c2ccccc2)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.54
ALDH1A1 P00352 4/20 0.52
L3MBTL1 Q9Y468 3/20 0.52
KDM4E B2RXH2 2/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
HPGD P15428 1/20 0.52
GFER P55789 1/20 0.52
MAPT P10636 3/20 0.50
RAB9A P51151 3/20 0.50
LMNA P02545 2/20 0.50
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2C9 P11712 1/20 0.47
ATM Q13315 1/20 0.47
TP53 P04637 1/20 0.47
CA1 P00915 1/20 0.47
MGLL Q99685 1/20 0.47
NPC1 O15118 1/20 0.46
MAPK1 P28482 1/20 0.46
MEN1 O00255 1/20 0.46

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
SCHEMBL4686720 1.00 KMT2A (0.54) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
SCHEMBL2445407 1.00 KMT2A (0.54) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
SCHEMBL29936503 0.92 ASIC1 (0.54) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
SCHEMBL29936120 0.92 ASIC1 (0.54) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
Benzaldehyde Oxime SCHEMBL266504 0.85
Benzaldehyde Oxime SCHEMBL309201 0.85
Benzaldehyde Oxime SCHEMBL220641 0.85
Benzaldehyde Oxime SCHEMBL9761423 0.82 L3MBTL1 (0.57) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
Benzaldehyde Oxime SCHEMBL10645128 0.82 L3MBTL1 (0.57) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2
Benzaldehyde Oxime SCHEMBL4607427 0.82 L3MBTL1 (0.57) KMT2AALDH1A1L3MBTL1KDM4ESMN1; SMN2

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
CN-107488090-B Efficient catalytic asymmetric preparation method of N-cyclopropyl nitrone compound 东北师范大学 2020-06-02 CN claimed
WO-1998005630-A1 PROCESS FOR THE PREPARATION OF ORGANIC NITRILES ALLIEDSIGNAL INC. (US) 1998-02-12 WO claimed
US-12570675-B2 Boronic acid compounds LG CHEM, LTD. (KR) 2026-03-10 US disclosed
US-20240101579-A1 BORONIC ACID COMPOUNDS LG CHEM, LTD. (KR) 2024-03-28 US disclosed
EP-4242213-A1 BORONIC ACID COMPOUND Lg Chem, Ltd. (KR) 2023-09-13 EP disclosed
CN-116568310-A Boric acid compounds 株式会社LG化学 2023-08-08 CN disclosed
WO-2022123530-A1 BORONIC ACID COMPOUND 주식회사 엘지화학 2022-06-16 WO disclosed
CN-107488090-B Efficient catalytic asymmetric preparation method of N-cyclopropyl nitrone compound 东北师范大学 2020-06-02 CN disclosed
US-20190135765-A1 NOVEL PYRIMIDINE-4-CARBOXYLIC ACID DERIVATIVE HAVING ANTICANCER ACTIVITY INDUSTRY-UNIVERSITY COOPERATION FOUNDATION HANYANG UNIVERSITY (KR) 2019-05-09 US disclosed
US-20190135765-A1 NOVEL PYRIMIDINE-4-CARBOXYLIC ACID DERIVATIVE HAVING ANTICANCER ACTIVITY INDUSTRY-UNIVERSITY COOPERATION FOUNDATION HANYANG UNIVERSITY (KR) 2019-05-09 US disclosed
WO-2018170167-A1 FARNESOID X RECEPTOR AGONISTS AND USES THEREOF METACRINE, INC. (US) 2018-09-20 WO disclosed
US-5972959-A Oxime derivatives, their preparation and their therapeutic use SANKYO COMPANY, LIMITED (JP) 1999-10-26 US disclosed
EP-0708098-B1 Oxime derivatives, their preparation and their therapeutic use SANKYO CO (JP) 1999-03-03 EP disclosed
US-5780490-A A O-(2,4-OXA(OR THIA)ZOLIDINYL)PHENYLOXY(OR THIO OR AMINO) ALKYLOXIME; ALDOSE REDUCTASE INHIBITORS; ANTIDIABETIC AND -HYPOGLYCEMIC AGENTS; LIVER, SKIN AND UROGENITAL DISORDERS SANKYO COMPANY, LIMITED (JP) 1998-07-14 US disclosed
WO-1998005630-A1 PROCESS FOR THE PREPARATION OF ORGANIC NITRILES ALLIEDSIGNAL INC. (US) 1998-02-12 WO disclosed
US-5703096-A ANTIDIABETIC AGENTS; ALDOSE REDUCTASE INHIBITOR SANKYO COMPANY, LIMITED (JP) 1997-12-30 US disclosed
CN-1143639-A Oxime derivatives, their preparation and their therapeutic use SANKYO CO (JP) 1997-02-26 CN disclosed
EP-0708098-A1 Oxime derivatives, their preparation and their therapeutic use SANKYO COMPANY LIMITED (JP) 1996-04-24 EP disclosed
EP-0559888-A1 THERMOSETTING POLYESTER PLASTIC COMPOSITIONS CONTAINING BLOCKED POLYISOCYANATE AND ISOCYANATE-REACTIVE MATERIAL UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1993-09-15 EP disclosed
WO-1993007216-A1 THERMOSETTING POLYESTER PLASTIC COMPOSITIONS CONTAINING BLOCKED POLYISOCYANATE AND ISOCYANATE-REACTIVE MATERIAL UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1993-04-15 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 (3 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-12570675-B2 Boronic acid compounds PSMB6, PSMB3, PSMB2 KMT2A 2072/4885ALDH1A1 3621/4885L3MBTL1 393/4885
US-20240101579-A1 BORONIC ACID COMPOUNDS PSMB11, PSMB1, BACH1 KMT2A 1197/4885ALDH1A1 2005/4885L3MBTL1 599/4885
US-20190135765-A1 NOVEL PYRIMIDINE-4-CARBOXYLIC ACID DERIVATIVE HAVING ANTICANCER ACTIVITY DPYD, TYMS, TYMP KMT2A 2256/4885ALDH1A1 153/4885L3MBTL1 2361/4885

“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.