SCHEMBL8077362

SCHEMBL8077362

[NH]C(=O)c1ccc[nH]c1=O

nearest known ligand 0.67

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 1/20 0.67
DAO P14920 1/20 0.50
TYK2 P29597 1/20 0.46
AURKA O14965 1/20 0.45
AURKB Q96GD4 1/20 0.45
INCENP Q9NQS7 1/20 0.45
RAB9A P51151 2/20 0.44
MAPT P10636 2/20 0.44
KDM4E B2RXH2 2/20 0.44
GAA P10253 2/20 0.44
TSHR P16473 1/20 0.43
NPC1 O15118 1/20 0.42
SMYD3 Q9H7B4 1/20 0.41
MCL1 Q07820 1/20 0.41
MAPK1 P28482 1/20 0.40
ALDH1A1 P00352 1/20 0.38
RECQL P46063 1/20 0.38

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
SCHEMBL425117 0.82 NAPRT (0.72) NAPRTDAOTYK2AURKAAURKB
SCHEMBL8193694 0.82 NAPRT (0.72) NAPRTDAOTYK2AURKAAURKB
SCHEMBL440492 0.80 NAPRT (1.00) NAPRTDAOTYK2AURKAAURKB
SCHEMBL82637 0.78 NAPRT (0.67) NAPRTDAOTYK2AURKAAURKB
Hydrochloric Acid SCHEMBL17597625 0.78 NAPRT (0.96) NAPRTDAOTYK2AURKAAURKB
SCHEMBL3182033 0.78 NAPRT (0.67) NAPRTDAOTYK2AURKAAURKB
Hydrochloric Acid SCHEMBL14741024 0.78 NAPRT (0.96) NAPRTDAOTYK2AURKAAURKB
SCHEMBL2281551 0.78 NAPRT (0.67) NAPRTDAOTYK2AURKAAURKB
SCHEMBL30750784 0.78 NAPRT (0.67) NAPRTDAOTYK2AURKAAURKB
SCHEMBL5943030 0.77 NAPRT (0.59) NAPRTDAOTYK2AURKAAURKB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0511002-A2 C-3 phosphine oxide substituted carbacephalosporins ELI LILLY AND COMPANY (US) 1992-10-28 EP claimed
EP-0494733-A1 Trifluoromethyl 1-carba(1-dethia)cephems ELI LILLY AND COMPANY (US) 1992-07-15 EP claimed
US-5099015-A Antibiotics formed by bromination of trifluoromethanesulfonyl containing cephalosporins ELI LILLY AND COMPANY (US) 1992-03-24 US claimed
US-5084447-A Antibiotics as bactericides ELI LILLY AND COMPANY (US) 1992-01-28 US claimed
EP-0565351-B1 Process for preparing 7-substituted-amino-3-hydroxy-3-cephem-4-protected carboxy-sulfoxide esters LILLY CO ELI (US) 2000-08-23 EP disclosed
EP-0494118-B1 Process for 3-exomethylenecepham sulfoxide esters LILLY CO ELI (US) 1997-04-09 EP disclosed
US-5512454-A Enzymatic acylation of 3-hydroxymethyl cephalosporins BRISTOL-MYERS SQUIBB COMPANY (US) 1996-04-30 US disclosed
US-5453502-A 1,3,4 substituted and bicyclic derivatives of 2-azetidinones and processes for preparation thereof ELI LILLY AND COMPANY (US) 1995-09-26 US disclosed
EP-0672656-A1 1,3,4 substituted and bicyclic derivatives of 2-azetidinones and processes for preparation thereof ELI LILLY AND COMPANY (US) 1995-09-20 EP disclosed
EP-0667396-A1 Enzymatic acylation of 3-hydroxymethyl cephalosporins BRISTOL-MYERS SQUIBB COMPANY (US) 1995-08-16 EP disclosed
US-5350845-A Process for preparing 7-substituted-amino-3-hydroxy-3-cephem-4-protected carboxy-sulfoxide esters ELI LILLY AND COMPANY (US) 1994-09-27 US disclosed
EP-0565351-A2 Process for preparing 7-substituted-amino-3-hydroxy-3-cephem-4-protected carboxy-sulfoxide esters ELI LILLY AND COMPANY (US) 1993-10-13 EP disclosed
US-5221739-A Acetylation of 3-hydroxymethyl cephalosporins ELI LILLY AND COMPANY (US) 1993-06-22 US disclosed
EP-0511002-A2 C-3 phosphine oxide substituted carbacephalosporins ELI LILLY AND COMPANY (US) 1992-10-28 EP disclosed
EP-0494733-A1 Trifluoromethyl 1-carba(1-dethia)cephems ELI LILLY AND COMPANY (US) 1992-07-15 EP disclosed
EP-0494118-A1 Process for 3-exomethylenecepham sulfoxide esters ELI LILLY AND COMPANY (US) 1992-07-08 EP disclosed
US-5126446-A Cyclization of 3-methyl-2-(4-chlorosulfinyl-2-oxo-3-amino-1-azetidinyl)-3-butenoic acid esters using lewis acid friedel-crafts catalyst, nitro compound, anhydrous conditions ELI LILLY AND COMPANY (US) 1992-06-30 US disclosed
US-5099015-A Antibiotics formed by bromination of trifluoromethanesulfonyl containing cephalosporins ELI LILLY AND COMPANY (US) 1992-03-24 US disclosed
US-5084447-A Antibiotics as bactericides ELI LILLY AND COMPANY (US) 1992-01-28 US disclosed