SCHEMBL5265771

SCHEMBL5265771

COC(=O)CCOS(C)(=O)=O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.52
CA12 O43570 5/20 0.48
CA14 Q9ULX7 5/20 0.48
LMNA P02545 4/20 0.48
ALDH1A1 P00352 3/20 0.48
USP2 O75604 2/20 0.48
KDM4E B2RXH2 2/20 0.48
MMP9 P14780 1/20 0.48
ALOX15 P16050 1/20 0.48
KMT2A Q03164 2/20 0.40
MEN1 O00255 1/20 0.40
CA7 P43166 3/20 0.39
CA9 Q16790 3/20 0.39
CA2 P00918 1/20 0.38
HSD17B10 Q99714 2/20 0.38
FNTA P49354 1/20 0.38
FNTB P49356 1/20 0.38
MAPT P10636 1/20 0.38
HTT P42858 1/20 0.38
MGAM O43451 1/20 0.37

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
SCHEMBL12092174 0.88 TSHR (0.44) TSHRCA12CA14LMNAALDH1A1
SCHEMBL1193812 0.84 TSHR (0.58) TSHRCA12CA14LMNAALDH1A1
SCHEMBL11885392 0.84 TSHR (0.58) TSHRCA12CA14LMNAALDH1A1
SCHEMBL14654893 0.82 FNTA (0.53) TSHRCA12CA14LMNAALDH1A1
SCHEMBL13642687 0.81 TSHR (0.41) TSHRCA12CA14LMNAALDH1A1
SCHEMBL27432690 0.80 USP2 (0.46) TSHRLMNAALDH1A1USP2KDM4E
SCHEMBL6910514 0.80 TSHR (0.50) TSHRCA12CA14LMNAALDH1A1
SCHEMBL9657895 0.78 CYP1A2 (0.45) TSHRLMNAALDH1A1USP2KDM4E
SCHEMBL3265255 0.78 TSHR (0.48) TSHRCA12CA14LMNAALDH1A1
SCHEMBL15697255 0.78 TSHR (0.41) TSHRCA12CA14LMNAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1735297-B1 SYNTHESISING METHOD AND BENZOXATHIEPINE INTERMEDIATES PF MEDICAMENT (FR) 2007-10-03 EP claimed
EP-1735297-A1 SYNTHESISING METHOD AND BENZOXATHIEPINE INTERMEDIATES PIERRE FABRE MEDICAMENT (FR) 2006-12-27 EP claimed
WO-2005103027-A1 SYNTHESISING METHOD AND BENZOXATHIEPINE INTERMEDIATES PIERRE FABRE MEDICAMENT (FR) 2005-11-03 WO claimed
WO-2023104165-A1 PYRIDINE[4,3-D]PYRIMIDINE COMPOUND AS TLR7/8 AGONIST 上海维申医药有限公司 2023-06-15 WO disclosed
CN-108707115-A A kind of synthetic method of acrylic acid derivative 成都道合尔医药技术有限公司 2018-10-26 CN disclosed
CN-1800140-A Method for preparing enantiomer enriched 2-fluorim carboxylic ester LANXESS DEUTSCHLAND GMBH (DE) 2006-07-12 CN disclosed
EP-1254109-B1 CATIONIC DYEABILITY MODIFIER FOR USE WITH POLYESTER AND POLYAMIDE INVISTA TECH SARL (US) 2005-11-02 EP disclosed
EP-1155616-B1 Process for the preparation of (N-phenylacetyl-N-2,6-xylil)methyl alaninate ISAGRO SPA (IT) 2003-01-29 EP disclosed
EP-1254109-A1 CATIONIC DYEABILITY MODIFIER FOR USE WITH POLYESTER AND POLYAMIDE E. I. du Pont de Nemours and Company (US) 2002-11-06 EP disclosed
EP-0946093-B1 FUNGICIDAL COMPOSITIONS BASED ON (N-PHENYLACETYL-N-2,6-XYLYL)METHYL ALANINATE ISAGRO SPA (IT) 2002-08-28 EP disclosed
EP-1155616-A1 Process for the preparation of (N-phenylacetyl-N-2,6-xylil)methyl alaninate ISAGRO S.p.A. (IT) 2001-11-21 EP disclosed
US-6312805-B1 (ALKALI METAL SULFOETHYL)ALKYLENEDIOIC ACID AND ESTERS; COPOLYMERIZATION WITH POLYESTER OR POLYAMIDE MONOMERS E.I. DU PONT DE NEMOURS AND COMPANY 2001-11-06 US disclosed
WO-2001058863-A1 CATIONIC DYEABILITY MODIFIER FOR USE WITH POLYESTER AND POLYAMIDE E. I. DU PONT DE NEMOURS AND COMPANY (US) 2001-08-16 WO disclosed
US-6228885-B1 Fungicidal compositions based on (N-phenylacetyl-N-2,6-XYLYL)methyl alaninate ISAGRO S.P.A. (IT) 2001-05-08 US disclosed
EP-0946093-A2 FUNGICIDAL COMPOSITIONS BASED ON (N-PHENYLACETYL-N-2,6-XYLYL)METHYL ALANINATE ISAGRO S.p.A. (IT) 1999-10-06 EP disclosed
WO-1998026654-A2 FUNGICIDAL COMPOSITIONS BASED ON (N-PHENYLACETYL-N-2,6-XYLYL)METHYL ALANINATE ISAGRO S.P.A. (IT) 1998-06-25 WO disclosed