SCHEMBL7769020

SCHEMBL7769020

C=CCOC(=O)[C@H](CCCCS(C)(=O)=O)NC(=O)OC(C)(C)C

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.49
CTSK P43235 10/20 0.40
CTSS P25774 3/20 0.39
HDAC4 P56524 4/20 0.37
HDAC1 Q13547 4/20 0.37
HDAC6 Q9UBN7 2/20 0.37
CYP1A2 P05177 1/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
HTT P42858 1/20 0.37
ALDH1A1 P00352 1/20 0.36
TSHR P16473 1/20 0.36
HDAC3 O15379 1/20 0.35
HDAC7 Q8WUI4 1/20 0.35
HDAC2 Q92769 1/20 0.35
HDAC10 Q969S8 1/20 0.35
HDAC11 Q96DB2 1/20 0.35
HDAC8 Q9BY41 1/20 0.35
HDAC9 Q9UKV0 1/20 0.35
HDAC5 Q9UQL6 1/20 0.35

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
SCHEMBL7769022 1.00 SMN1; SMN2 (0.49) SMN1; SMN2CTSKCTSSHDAC4HDAC1
SCHEMBL7695305 0.85 SMN1; SMN2 (0.53) SMN1; SMN2CTSKCTSSHDAC4HDAC1
SCHEMBL7690020 0.84 SMN1; SMN2 (0.52) SMN1; SMN2CTSKCTSSHDAC4HDAC1
SCHEMBL7765475 0.84 SMN1; SMN2 (0.52) SMN1; SMN2CTSKCTSSHDAC4HDAC1
SCHEMBL27429588 0.82 SMN1; SMN2 (0.50) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9
SCHEMBL6722516 0.81 SMN1; SMN2 (0.56) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9
SCHEMBL6722519 0.81 SMN1; SMN2 (0.56) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9
SCHEMBL6719127 0.81 SMN1; SMN2 (0.56) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9
SCHEMBL27429586 0.80 SMN1; SMN2 (0.55) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9
SCHEMBL4427686 0.80 SMN1; SMN2 (0.55) SMN1; SMN2CTSKCTSSCYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1105415-A1 CHEMICAL SYNTHESIS OF EXOCHELINS Keystone Biomedical, Inc. (US) 2001-06-13 EP disclosed
WO-2000009548-A1 CHEMICAL SYNTHESIS OF EXOCHELINS KEYSTONE BIOMEDICAL, INC. (US) 2000-02-24 WO disclosed
US-5952492-A REACTING A MIXTURE OF DIACID WITH DIMETHYL PIMELATE, HYDROCHLORIC ACID, METHANOL, DIBUTYL ETHER TO FORM INTERMEDIATE, ADDING O-BENZYL HYDROXYLAMINE HYDROCHLORIDE AND TRIETHYLAMINE, ADDITING DI-TERT-BUTYL DICARBONATE KEYSTONE BIOMEDICAL, INC. (US) 1999-09-14 US disclosed