SCHEMBL7167696

SCHEMBL7167696

COc1ccc(C2NC(=O)NC2=O)cc1

nearest known ligand 0.69

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.67
MAPT P10636 2/20 0.67
LMNA P02545 1/20 0.63
KDM4E B2RXH2 3/20 0.61
TP53 P04637 1/20 0.61
TDP1 Q9NUW8 1/20 0.61
GAA P10253 3/20 0.55
HPGD P15428 1/20 0.53
CASP1 P29466 1/20 0.53
MPI P34949 1/20 0.53
HSD17B10 Q99714 1/20 0.53
DDB1 Q16531 1/20 0.51
CRBN Q96SW2 1/20 0.51
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
RXFP1 Q9HBX9 1/20 0.47

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
SCHEMBL10536959 0.85 KDM4E (0.56) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL13527924 0.84 TDP1 (0.80) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL14467187 0.82 ALDH1A1 (0.76) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL31312297 0.82 ALDH1A1 (0.76) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL11652811 0.82 ALDH1A1 (0.50) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL17570757 0.81 MAPT (0.61) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL11153022 0.81 ALDH1A1 (0.61) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL11647775 0.80 DDB1 (0.56) ALDH1A1MAPTLMNAGAADDB1
SCHEMBL9690927 0.79 TDP1 (0.67) ALDH1A1MAPTLMNAKDM4ETP53
SCHEMBL14466166 0.79 TDP1 (0.67) ALDH1A1MAPTLMNAKDM4ETP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6566105-B1 Generation of preferential amino acids in sample; obtain racemic mixture of hydantoin, incubate with genetically engineered microorganism, recover amino acids ENIRICERCHE S.P.A. (IT) 2003-05-20 US claimed
EP-0775748-B1 Preparation of D-alpha-amino acids, using bacteria transformed with the carbamoylase-hydantoinase operon ENITECNOLOGIE SPA (IT) 2002-11-20 EP claimed
US-5834258-A STEREOSELECTIVE CONVERSION OF RACEMIC MIXTURES OF 5-SUBSTITUTED HYDANTOINS WITH ENZYME ENIRICERCHE S.P.A. (IT) 1998-11-10 US claimed
EP-0677585-B1 Process for the production of D-alpha-amino acids ENIRICERCHE SPA (IT) 1997-07-23 EP claimed
EP-0775748-A2 Preparation of D-alpha-amino acids, using bacteria transformed with the carbamoylase-hydantoinase operon ENIRICERCHE S.p.A. (IT) 1997-05-28 EP claimed
EP-0677585-A1 Process for the production of D-alpha-amino acids ENIRICERCHE S.p.A. (IT) 1995-10-18 EP claimed
US-4094741-A CULTURES, ASYMMETRIC HYDROLYSIS KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JA) 1978-06-13 US claimed
US-20240390488-A1 METHODS OF TREATING CANCER USING PD-1 AXIS BINDING ANTAGONISTS AND MEK INHIBITORS GENENTECH, INC. (US) 2024-11-28 US disclosed
US-6566105-B1 Generation of preferential amino acids in sample; obtain racemic mixture of hydantoin, incubate with genetically engineered microorganism, recover amino acids ENIRICERCHE S.P.A. (IT) 2003-05-20 US disclosed
EP-0775748-B1 Preparation of D-alpha-amino acids, using bacteria transformed with the carbamoylase-hydantoinase operon ENITECNOLOGIE SPA (IT) 2002-11-20 EP disclosed
US-5877002-A ENZYME FROM AGROBACTERIUM RADIOBACTER WITH AMINO ACID SUBSTITUTIONS, FOR EFFICIENT PRODUCTION OF D-ALPHA AMINO ACIDS USED IN CHEMICAL INTERMEDIATES FOR SWEETNERS, INSECTICIDES, CEPHALOSPORINS, PENICILLINS ENIRICERCHE S.P.A. (IT) 1999-03-02 US disclosed
US-5877003-A NUCLEOTIDE SEQUENCE FOR ENZYME USED TO EFFICIENTY PRODUCE D-ALPHA AMINO ACIDS; USED AS CHEMICAL INTERMEDIATES FOR SWEETENERS, INSECTICIDES AND SEMI-SYNTHETIC PENICILLINS AND CEPHALOSPORINS ENIRICERCHE S.P.A (IT) 1999-03-02 US disclosed
US-5869298-A Stable mutants of D-N-α-carbamoylase and process for preparing D-α-amino acids ENIRICERCHE S.P.A. (IT) 1999-02-09 US disclosed
EP-0677585-A1 Process for the production of D-alpha-amino acids ENIRICERCHE S.p.A. (IT) 1995-10-18 EP disclosed
EP-0647630-A1 Process for producing 5-arylhydantoins SHOWA DENKO KABUSHIKI KAISHA (JP) 1995-04-12 EP disclosed
WO-1988005653-A1 TOPICAL COMPOSITION FOR STIMULATING HAIR GROWTH WITH STABLE FREE RADICALS PROCTOR PETER H (US) 1988-08-11 WO disclosed
US-4418146-A CBS 303.80 OR CBS 363.50 THERMOPHILIC, NON-SPORULATING STRAINS BASF AKTIENGESELLSCHAFT (DE) 1983-11-29 US disclosed
US-4281009-A SEDATIVES, ANALGESICS, ANTIULCER AGENTS, A HYPNOTIC AND ANTIHYPERTENSIVE AGENTS NIPPON ZOKI PHARMACEUTICAL CO., LTD. (JP) 1981-07-28 US disclosed
US-4094741-A CULTURES, ASYMMETRIC HYDROLYSIS KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JA) 1978-06-13 US disclosed
US-4065353-A Method for the preparation of D-carbamyl aminoacids and the corresponding D-aminoacids SNAMPROGETTI, S.P.A. (IT) 1977-12-27 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-20240390488-A1 METHODS OF TREATING CANCER USING PD-1 AXIS BINDING ANTAGONISTS AND MEK INHIBITORS CD274, PDCD1, PDCD1LG2 ALDH1A1 2289/4885MAPT 3861/4885LMNA 4140/4885

“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.