SCHEMBL751213

SCHEMBL751213

CC(NC(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.77
SMN1; SMN2 Q16637 2/20 0.77
LMNA P02545 2/20 0.77
NPC1 O15118 1/20 0.77
ROCK2 O75116 1/20 0.69
RPS6KA5 O75582 1/20 0.69
MAP4K4 O95819 1/20 0.69
CDK1 P06493 1/20 0.69
CSF1R P07333 1/20 0.69
PRKACA P17612 1/20 0.69
FLT1 P17948 1/20 0.69
RPS6KB1 P23443 1/20 0.69
CDK2 P24941 1/20 0.69
MAPK1 P28482 1/20 0.69
AKT1 P31749 1/20 0.69
FLT4 P35916 1/20 0.69
KDR P35968 1/20 0.69
FLT3 P36888 1/20 0.69
GSK3A P49840 1/20 0.69
GSK3B P49841 1/20 0.69

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
SCHEMBL5968858 1.00 ALDH1A1 (0.77) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL1101522 1.00 ALDH1A1 (0.77) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL28651689 0.89 SMN1; SMN2 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL9318785 0.89 SMN1; SMN2 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL17369057 0.89 ALDH1A1 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL29135907 0.89 SMN1; SMN2 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL3755011 0.89 ALDH1A1 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL3756762 0.89 ALDH1A1 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL2919150 0.89 ALDH1A1 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2
SCHEMBL13947536 0.89 ALDH1A1 (0.73) ALDH1A1SMN1; SMN2LMNANPC1ROCK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190177707-A1 CARBOXYESTERASE POLYPEPTIDES FOR AMIDE COUPLING INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT 2019-06-13 US claimed
EP-3303291-A1 ROR GAMMA (ROR ) MODULATORS Lead Pharma Holding B.V. (NL) 2018-04-11 EP claimed
WO-2016193452-A1 ROR GAMMA (RORγ) MODULATORS LEAD PHARMA CEL MODELS IP B.V. (NL) 2016-12-08 WO claimed
US-9096768-B2 Curable phase change ink compositions XEROX CORPORATION (US) 2015-08-04 US claimed
US-12286653-B2 Carboxyesterase polypeptides for amide coupling CODEXIS, INC. (US) 2025-04-29 US disclosed
CN-119684070-A HFIP power assisting C (sp3) Direct methylation method of-H bond and application thereof 西南大学 2025-03-25 CN disclosed
US-20240353322-A1 COMBINED DETERMINATION OF THE CONCENTRATION AND ENANTIOMERIC COMPOSITION OF CHIRAL COMPOUNDS USING SINGLE CHIROPTICAL ASSAY GEORGETOWN UNIVERSITY 2024-10-24 US disclosed
US-20240261296-A1 THERAPEUTIC MODALITIES FOR INHIBITING PANCREATIC BETA CELL IMPAIRMENT AND TREATING DIABETES Hadasit Medical Research Serices & Development Ltd. (IL) 2024-08-08 US disclosed
EP-4319734-A2 PROSTAGLANDIN RECEPTOR 3 (EP3) ANTAGONISTS FOR USE IN THE TREATMENT OF DIABETES Hadasit Medical Research Services&Development Ltd. (IL) 2024-02-14 EP disclosed
EP-3489215-B1 PROCESS FOR PRODUCING ORGANIC COMPOUND KANEKA CORP (JP) 2023-12-20 EP disclosed
EP-3475308-B1 USE OF 2,4,6-SUBSTITUTED-1,3,5-TRIAZINES AND DERIVATIVE THEREOF AS CONDENSATION, CROSS-LINKING, TANNING, GRAFTING AND CURING AGENTS CROSSING S R L (IT) 2023-01-25 EP disclosed
WO-2022215072-A2 THERAPEUTIC MODALITIES FOR INHIBITING PANCREATIC BETA CELL IMPAIRMENT AND TREATING DIABETES HADASIT MEDICAL RESEARCH SERVICES & DEVELOPMENT LTD. (IL) 2022-10-13 WO disclosed
EP-1049691-A1 SUBSTITUTED 5-(2,2-DIFLUORO-1,3-BENZODIOXOL-5-YL) CYCLOPENTENOPYRIDINE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2000-11-08 EP disclosed
WO-1999037639-A1 SUBSTITUTED 5-(2,2-DIFLUORO-1,3-BENZODIOXOL-5-YL) CYCLOPENTENOPYRIDINE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 1999-07-29 WO disclosed
EP-0270095-B1 PACKING MATERIAL FOR LIQUID CHROMATOGRAPHY Tosoh Corporation (JP) 1991-11-13 EP disclosed
US-4830921-A RESOLUTION OF RACEMIC MIXTURES TOSOH CORPORATION (JP) 1989-05-16 US disclosed
EP-0158526-B1 IMPROVEMENTS IN OR RELATING TO ANTICONVULSANT AGENTS ELI LILLY AND COMPANY (US) 1987-07-08 EP disclosed
EP-0078845-A4 ANTI-CONVULSANT. CLARK CHARLES RANDALL 1983-09-02 EP disclosed
EP-0078845-A1 ANTI-CONVULSANT. CLARK CHARLES RANDALL 1983-05-18 EP disclosed
WO-1982004046-A1 ANTI-CONVULSANT CLARK CHARLES RANDALL 1982-11-25 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-20240261296-A1 THERAPEUTIC MODALITIES FOR INHIBITING PANCREATIC BETA CELL IMPAIRMENT AND TREATING DIABETES IAPP, PTGER3, GPR119 ALDH1A1 2596/4885SMN1; SMN2 1885/4885LMNA 2133/4885

“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.