SCHEMBL787583

SCHEMBL787583

N=C(N)NC(=O)[C]=O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL7697745 0.76
Biguanide SCHEMBL17701180 0.69 LDHA (0.35)
Biguanide SCHEMBL4198353 0.69 ACHE (0.40)
SCHEMBL3080488 0.69 LMNA (0.33)
SCHEMBL9809865 0.69 LMNA (0.33)
SCHEMBL146394 0.69
Biguanide SCHEMBL18255803 0.67 MAPK1 (0.31)
Biguanide SCHEMBL8039 0.67
Biguanide SCHEMBL8973572 0.67 ACHE (0.38)
Bromide SCHEMBL10501190 0.67

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9040553-B2 Phenoxyisobutyric acid compounds and method of synthesis Cell Viable Corporation (US) 2015-05-26 US disclosed
US-20140371316-A1 DERIVATIVES OF PHENOXYISOBUTYRIC ACID FABRICANT JILL S (US) 2014-12-18 US disclosed
US-20140350045-A1 PHENOXYISOBUTYRIC ACID COMPOUNDS AND METHOD OF SYNTHESIS LALEZARI IRAJ (US) 2014-11-27 US disclosed
EP-2616430-A2 NOVEL PHENOXYISOBUTYRIC ACID COMPOUNDS AND METHODS FOR SYNTHESIS Cell Viable Corporation (US) 2013-07-24 EP disclosed
US-20120232120-A1 AMINO ACID AMIDES OF PHENOXYBUTYRIC ACID DERIVATIVES LALEZARI IRAJ (US) 2012-09-13 US disclosed
WO-2012050623-A2 NOVEL PHENOXYISOBUTYRIC ACID COMPOUNDS AND METHODS FOR SYNTHESIS Cell Viable Corporation (US) 2012-04-19 WO disclosed
US-20120071502-A1 Novel phenoxyisobutyric acid compounds and methods for synthesis Cell Viable Corporation (US) 2012-03-22 US disclosed
US-8034966-B1 Phenoxyisobutyric acid compounds and methods for synthesis Cell Viable Corporation (US) 2011-10-11 US disclosed
EP-1594492-B1 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGES) HOPE CITY (US) 2008-11-26 EP disclosed
EP-1370256-B1 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGES) HOPE CITY (US) 2007-05-02 EP disclosed
US-7030133-B2 Inhibitors of formation of advanced glycation endproducts (AGEs) CITY OF HOPE (US) 2006-04-18 US disclosed
US-20030220362-A1 Novel inhibitors of formation of advanced glycation endproducts (AGEs) CITY OF HOPE 2003-11-27 US disclosed
US-6605642-B2 Administering specified compounds which are derivatives of phenoxyisobutyric acids and of benzoic acid including aryl and heterocyclic ureido derivatives and aryl and heterocyclic carboxamido derivatives; treating aging, arthritis, diabetes CITY OF HOPE 2003-08-12 US disclosed
US-20020013256-A1 Novel inhibitors of formation of advanced glycation endproducts (AGES) PROSCIENCE CORPORATION, INCORPORATED IN THE STATE OF NEW YORK 2002-01-31 US disclosed
US-4977189-A Anxiolytic agents, cognition activators AMERICAN CYANAMID COMPANY (US) 1990-12-11 US disclosed
US-4977189-A Anxiolytic agents, cognition activators AMERICAN CYANAMID COMPANY (US) 1990-12-11 US disclosed
US-4977189-A Anxiolytic agents, cognition activators AMERICAN CYANAMID COMPANY (US) 1990-12-11 US disclosed