SCHEMBL7960923

SCHEMBL7960923

B.CCCCSCCCC

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.43
LMNA P02545 2/20 0.43
CES1 P23141 5/20 0.42
CES2 O00748 3/20 0.40
THRB P10828 2/20 0.40
MAPT P10636 2/20 0.40
GMNN O75496 1/20 0.40
TP53 P04637 1/20 0.40
POLB P06746 1/20 0.40
CYP2C9 P11712 1/20 0.40
BLM P54132 1/20 0.40
HSD17B10 Q99714 1/20 0.40
NOS3 P29474 1/20 0.39
NOS1 P29475 1/20 0.39
NOS2 P35228 1/20 0.39
CA2 P00918 1/20 0.39
GBA1 P04062 1/20 0.36
ATM Q13315 1/20 0.36
FAAH O00519 4/20 0.34
PLA2G6 O60733 1/20 0.34

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
SCHEMBL21882 0.96
SCHEMBL6689804 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL1406213 0.92 CES2 (0.46) TSHRLMNACES1CES2THRB
SCHEMBL11525884 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL4849581 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL11531992 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
Iodide SCHEMBL7869089 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL11527395 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL747847 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB
SCHEMBL10591515 0.92 TSHR (0.43) TSHRLMNACES1CES2THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-100374411-C Process for preparing racemic or optically active 4- (hydroxymethyl) -2-cyclopentene derivatives LONZA CO LTD (CH) 2008-03-12 CN disclosed
CN-1302116-C Process for preparing enantiomers of (1R, 4S) -or (1S, 4R) -1-amino-4- (hydroxymethyl) -2-cyclopentene derivatives LONZE AG (CH) 2007-02-28 CN disclosed
CN-1827591-A Process for preparing racemic or optically active 4- (hydroxymethyl) -2-cyclopentene derivatives LONZA AG (CH) 2006-09-06 CN disclosed
CN-1515673-A Process for preparing enantiomers of (1R, 4S) -or (1S, 4R) -1-amino-4- (hydroxymethyl) -2-cyclopentene derivatives ��¡���ӹɷ����޹�˾ 2004-07-28 CN disclosed
CN-1115343-C Process for the preparation of (1S,4R) -or (1R,4S) -4- (2-amino-6-chloro-9H-purin-9-yl) -2-cyclopentene-1-methanol or salts thereof LONZA AG (CH) 2003-07-23 CN disclosed
US-6262295-B1 REACTING CYCLOPENTENE-4-CARBOXYLIC ACID WITH AN ACYL HALIDE LONZA A.G. (CH) 2001-07-17 US disclosed
US-6252112-B1 MIBCROBIAL HYDROLYSIS OF THE TITLE COMPOUND DERIVATIVE USING ENZYME HAVING N-ACETYLAMINO-ALCOHOL HYDROLASE OR PENICILLIN G ACYLASE ACTIVITY WITH SUBSEQUENT ACYLATION LONZA A.G., (CH) 2001-06-26 US disclosed
US-6156893-A Process for the preparation of (1S,4R)- or (1R,4S)- 4-(2-amino-6-chloro-9H-purin-9-yl)-2-cyclopentene-1-methanol LONZA A.G. (CH) 2000-12-05 US disclosed
US-6137007-A CHEMICAL INTERMEDIATES FOR NUCLEOSIDE, 4-2-(AMINO-6-CHLORO-9H-PURIN-9-YL)-2-CYCLOPENTENE-1-METHANOL, WHICH IS AN INTERMEDIATE FOR 6-(CYCLOPROPYLAMINO)-DERIVATIVE LONZA AG (CH) 2000-10-24 US disclosed
CN-1201794-A Process for the preparation of (1S,4R) -or (1R,4S) -4- (2-amino-6-chloro-9H-purin-9-yl) -2-cyclopentene-1-methanol or salts thereof LONZA AG (CH) 1998-12-16 CN disclosed