SCHEMBL7899207

SCHEMBL7899207

NC(=S)c1ccccc1-c1ccc(CO)cc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCAT2 O15382 1/20 0.44
TSHR P16473 1/20 0.41
PDK2 Q15119 1/20 0.41
PARP1 P09874 1/20 0.38
PRSS1 P07477 1/20 0.38
PRSS2 P07478 1/20 0.38
PRSS3 P35030 1/20 0.38
LTB4R2 Q9NPC1 5/20 0.38
LTA4H P09960 1/20 0.37
MKNK1 Q9BUB5 1/20 0.37
MKNK2 Q9HBH9 1/20 0.37
CHRNB2 P17787 1/20 0.37
CHRNB4 P30926 1/20 0.37
CHRNA3 P32297 1/20 0.37
CHRNA4 P43681 1/20 0.37
MAOB P27338 2/20 0.36
BAZ2B Q9UIF8 1/20 0.36
BAZ2A Q9UIF9 1/20 0.36
NOS3 P29474 1/20 0.35
NOS1 P29475 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
SCHEMBL7897892 0.87 TAAR1 (0.48) BCAT2LTB4R2LTA4HMAOB
SCHEMBL7899173 0.86 TDP1 (0.45) BCAT2LTB4R2MAOB
SCHEMBL7889274 0.86 BCAT2 (0.42) BCAT2LTB4R2CHRNB2CHRNB4CHRNA3
SCHEMBL7897093 0.86 BCAT2 (0.42) BCAT2TSHRLTB4R2CHRNB2CHRNB4
SCHEMBL7896340 0.86 SMN1; SMN2 (0.52) BCAT2LTB4R2
SCHEMBL7900715 0.84 MAOB (0.56) BCAT2MAOBNOS3NOS1
SCHEMBL7889284 0.83 TDP1 (0.42) BCAT2LTB4R2MAOB
SCHEMBL7889269 0.83 PPARG (0.44) LTB4R2
SCHEMBL7899237 0.83 LPAR1 (0.42) BCAT2LTB4R2LTA4HMAOB
SCHEMBL709834 0.82 BCAT2 (0.63) BCAT2TSHRPARP1CHRNB2CHRNB4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6277998-B1 REACTING 2-CYANO-4-OXO-4H-BENZOPYRAN COMPOUND WITH HYDROGEN SULFIDE AND THEN REACTING PROUDCT WITH ALKYL HALIDE; REACTING THE PRODUCT WITH HYDRAZINE OR ITS SALT AND THEN WITH NITROUS ACID COMPOUND TO OBTAIN TETRAZOLE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-08-21 US disclosed
US-6191289-B1 REACTING A 4-OXO-4H-BENZOPYRAN GROUP SUBSTITUTED WITH AMIDE OR A PHENYL GROUP IN ITS 2 POSITION IS REACTED WITH ANHYDROUS HYDRAZINE OR SALT IN PRESENCE OF CATALYST FOLLOWED BY REACTING WITH NITROUS ACID OR SALT TO FORM TETRAZOLE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-02-20 US disclosed
US-5874593-A SULFUR CONTAINING AMIDE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1999-02-23 US disclosed
EP-0711762-A1 PROCESS FOR PRODUCING TETRAZOLE COMPOUND AND INTERMEDIATE THEREFOR SUMITOMO CHEMICAL COMPANY LIMITED (JP) 1996-05-15 EP disclosed