SCHEMBL774049

SCHEMBL774049

CC1CC(=O)N(c2ccccc2)C1=O

nearest known ligand 0.62

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.58
KDM4E B2RXH2 2/20 0.57
LMNA P02545 1/20 0.57
MT-CO2 P00403 6/20 0.55
ALOX5 P09917 6/20 0.55
MAPT P10636 3/20 0.54
GAA P10253 2/20 0.54
GFER P55789 2/20 0.54
TDP1 Q9NUW8 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54
POLB P06746 2/20 0.50

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
SCHEMBL3485977 1.00 ALDH1A1 (0.58) ALDH1A1KDM4ELMNAMT-CO2ALOX5
SCHEMBL28243691 1.00 ALDH1A1 (0.58) ALDH1A1KDM4ELMNAMT-CO2ALOX5
SCHEMBL16566170 0.90 ALDH1A1 (0.50) ALDH1A1KDM4ELMNAMAPTGAA
SCHEMBL822035 0.87 ALDH1A1 (0.49) ALDH1A1MAPTGAAGFERSMN1; SMN2
SCHEMBL13057572 0.84 GAA (0.52) ALDH1A1KDM4ELMNAMT-CO2ALOX5
SCHEMBL14821834 0.83 ALDH1A1 (0.61) ALDH1A1KDM4ELMNAMAPTGAA
SCHEMBL16566172 0.82 ALDH1A1 (0.44) ALDH1A1KDM4ELMNAMAPTGAA
SCHEMBL20375597 0.82 MAPT (0.42) ALDH1A1LMNAMAPTTDP1SMN1; SMN2
SCHEMBL16450893 0.81 HSP90AA1 (0.59) ALDH1A1LMNAMAPTGAASMN1; SMN2
SCHEMBL13057567 0.81 ALDH1A1 (0.51) ALDH1A1MT-CO2ALOX5MAPTGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0871439-A4 SUBSTITUTED (ARYL, HETEROARYL, ARYLMETHYL OR HETEROARYLMETHYL) HYDROXAMIC ACID COMPOUNDS RHONE POULENC RORER PHARMA (US) 1999-07-21 EP claimed
EP-0871439-A1 SUBSTITUTED (ARYL, HETEROARYL, ARYLMETHYL OR HETEROARYLMETHYL) HYDROXAMIC ACID COMPOUNDS RHONE-POULENC RORER PHARMACEUTICALS, INC. (US) 1998-10-21 EP claimed
WO-1997024117-A1 SUBSTITUTED (ARYL, HETEROARYL, ARYLMETHYL OR HETEROARYLMETHYL) HYDROXAMIC ACID COMPOUNDS RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1997-07-10 WO claimed
US-20240032209-A1 MALEIMIDE RESIN COMPOSITION, PREPREG, RESIN FILM, LAMINATED BOARD, PRINTED WIRING BOARD, AND SEMICONDUCTOR PACKAGE RESONAC CORPORATION (JP) 2024-01-25 US disclosed
US-20240032209-A1 MALEIMIDE RESIN COMPOSITION, PREPREG, RESIN FILM, LAMINATED BOARD, PRINTED WIRING BOARD, AND SEMICONDUCTOR PACKAGE RESONAC CORPORATION (JP) 2024-01-25 US disclosed
CN-107922347-B Novel imide derivatives and their use as pharmaceuticals 田边三菱制药株式会社 2022-06-28 CN disclosed
EP-2558127-B1 TARGETED PYRROLOBENZODIAZEPINE CONJUGATES SEAGEN INC (US) 2022-01-19 EP disclosed
WO-2020245283-A1 PYRROLOBENZODIAZEPINE-ANTIBODY CONJUGATES ADC THERAPEUTICS SA (CH) 2020-12-10 WO disclosed
CN-108587927-B (S)-selectivity organism catalyst 中山大学 2019-08-09 CN disclosed
CN-108587927-A (S)-selectivity organism catalyst 中山大学 2018-09-28 CN disclosed
EP-3309162-A1 TARGETED CONJUGATES OF PYRROLOBENZODIAZEPINES Seattle Genetics, Inc. (US) 2018-04-18 EP disclosed
EP-1959019-A1 Method for enzymatic reduction of alkene derivates BASF SE (DE) 2008-08-20 EP disclosed
WO-2008058951-A1 PROCESS FOR ENZYMATIC REDUCTION OF ALKENE DERIVATIVES BASF SE (DE) 2008-05-22 WO disclosed
WO-2008058951-A1 PROCESS FOR ENZYMATIC REDUCTION OF ALKENE DERIVATIVES BASF SE (DE) 2008-05-22 WO disclosed
US-20070173636-A1 Method for preparing polyfunctionalized peptides and/or proteins via native chemical ligation NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2007-07-26 US disclosed
US-7232805-B2 Cobalamin conjugates for anti-tumor therapy INFLABLOC PHARMACEUTICALS, INC. (US) 2007-06-19 US disclosed
US-7160856-B2 α-O-linked glycoconjugates, methods of preparation and uses thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2007-01-09 US disclosed
US-4847285-A 1-substituted phenyl-3-substituted methyl-pyrrolidine-2,5-diones and plant fungicide compositions containing same THE DOW CHEMICAL COMPANY (US) 1989-07-11 US disclosed
EP-0173284-A1 Substituted 1-phenyl-3-methyl-pyrrolidindiones, their manufacture and use as fungicides THE DOW CHEMICAL COMPANY (US) 1986-03-05 EP disclosed
US-4204970-A Lubricant compositions containing alkylated aromatic amino acid antioxidants STANDARD OIL COMPANY (INDIANA) (US) 1980-05-27 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 (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-20070173636-A1 Method for preparing polyfunctionalized peptides and/or proteins via native chemical ligation TXNL1, NGLY1, RXFP1 ALDH1A1 3808/4885KDM4E 2759/4885LMNA 2223/4885

“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.