SCHEMBL1633629

SCHEMBL1633629

O=C(Cl)Oc1nccs1

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
SCHEMBL27852103 0.83 ALDH1A1 (0.43)
SCHEMBL27478065 0.83 ALDH1A1 (0.43)
SCHEMBL5086027 0.79
SCHEMBL3559527 0.79
SCHEMBL28140898 0.79
SCHEMBL11688470 0.79 PKM (0.38)
SCHEMBL28000724 0.78 HTT (0.45)
SCHEMBL27521615 0.78 ALDH1A1 (0.40)
SCHEMBL7499725 0.78 HTT (0.45)
Hydrochloric Acid SCHEMBL28248957 0.78 ALDH1A1 (0.48)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2286670-A None JP disclosed
JP-4049290-A None JP disclosed
US-7932386-B2 Preparation of 2-amino-thiazole-5-carboxylic-acid derivatives BRISTOL-MYERS SQUIBB COMPANY (US) 2011-04-26 US disclosed
EP-1919885-B1 PREPARATION OF 2-AMINO-THIAZOLE-5-CARBOXYLIC-ACID DERIVATIVES BRISTOL MYERS SQUIBB CO (US) 2010-04-28 EP disclosed
US-20090030203-A1 PREPARATION OF 2-AMINO-THIAZOLE-5-CARBOXYLIC-ACID DERIVATIVES BRISTOL-MYERS SQUIBB COMPANY (US) 2009-01-29 US disclosed
US-7408069-B2 Preparation of 2-amino-thiazole-5-carboxylic-acid derivatives BRISTOL-MYERS SQUIBB COMPANY (US) 2008-08-05 US disclosed
EP-1919885-A1 PREPARATION OF 2-AMINO-THIAZOLE-5-CARBOXYLIC-ACID DERIVATIVES Brystol-Myers Squibb Company (US) 2008-05-14 EP disclosed
WO-2007019210-A1 PREPARATION OF 2-AMINO-THIAZOLE-5-CARBOXYLIC-ACID DERIVATIVES BRISTOL-MYERS SQUIBB COMPANY (US) 2007-02-15 WO disclosed
US-20070037978-A1 Amidating chloro-, methyl-, methoxy, ethyl- or ethoxy-substituted aniline with 2,3-dichloroacryloyl chloride, alkanoate salt and inorganic base to form an N-phenyl-2-chloro-3,3-dimethoxypropionamide (that is also claimed), which is reacted with thiourea to form a N-phenyl-2-aminothiazol-5-ylcarboxamide BRISTOL-MYERS SQUIBB COMPANY (US) 2007-02-15 US disclosed
JP-H0449290-A PRODUCTION OF OPTICALLY ACTIVE AMIDE DERIVATIVE MITSUI TOATSU CHEM INC 1992-02-18 JP disclosed
JP-H02286670-A MINERAL ACID SALTS OF THIAZOLE CARBOXYLIC ACID CHLORIDE AND PRODUCTION THEREOF MITSUI TOATSU CHEM INC 1990-11-26 JP disclosed