SCHEMBL8045983

SCHEMBL8045983

CCN(CC)C(=O)c1ccccc1SC1=C(C(=O)OCc2ccc([N+](=O)[O-])cc2)N2C(=O)C(C(C)O[Si](C)(C)C)[C@@H]2C1C

nearest known ligand 0.36

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.36
RAB9A P51151 2/20 0.36
PLCG1 P19174 1/20 0.36
ELANE P08246 7/20 0.34
AR P10275 1/20 0.32
POLB P06746 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HTT P42858 1/20 0.32
HTR2A P28223 1/20 0.31
PAX8 Q06710 1/20 0.31

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
SCHEMBL8040733 0.91 ELANE (0.40) L3MBTL1RAB9APLCG1ELANEHTT
SCHEMBL8046094 0.87 LMNA (0.45) L3MBTL1RAB9APLCG1ARSMN1; SMN2
SCHEMBL8039578 0.85 L3MBTL1 (0.36) L3MBTL1RAB9APLCG1ELANEAR
SCHEMBL8038835 0.85 L3MBTL1 (0.36) L3MBTL1RAB9APLCG1ELANESMN1; SMN2
SCHEMBL8695468 0.83 ESR1 (0.33)
SCHEMBL8039549 0.83 ESR1 (0.33)
SCHEMBL10862718 0.80 PLCG1 (0.40) L3MBTL1RAB9APLCG1ELANEPOLB
SCHEMBL10865984 0.80 PLCG1 (0.40) L3MBTL1RAB9APLCG1ELANEPOLB
SCHEMBL10862713 0.80 PLCG1 (0.40) L3MBTL1RAB9APLCG1ELANEPOLB
SCHEMBL9026674 0.78 PLCG1 (0.40) L3MBTL1RAB9APLCG1ELANEPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5614624-A THIO SUBSTITUTED, ANTIBIOTICS, CHEMICAL INTERMEDIATES SANKYO COMPANY, LIMITED (JP) 1997-03-25 US claimed
EP-0587436-A1 Process for preparing carbapenem and penem compounds and new compounds involved in that process SANKYO COMPANY LIMITED (JP) 1994-03-16 EP claimed
EP-0587436-B1 Process for preparing carbapenem and penem compounds and new compounds involved in that process SANKYO CO (JP) 2000-05-10 EP disclosed
US-5719275-A REACTING SILYL ENOL ETHER WITH AZETIDINONE DERIVATIVE TO FORM INTERMEDIATE FOR PENICILLIN-TYPE ANTIBIOTIC SANKYO COMPANY, LIMITED (JP) 1998-02-17 US disclosed
US-5681951-A REACTING PENICILLIN DERIVATIVE HAVING SULFINYL OR SULFONYL GROUP IN 2 POSITION WITH SUBSTITUTED MERCAPTAN IN PRESENCE OF SALT OF GROUP IIA OR IIIA ELEMENT SANKYO COMPANY, LIMITED (JP) 1997-10-28 US disclosed
US-5614624-A THIO SUBSTITUTED, ANTIBIOTICS, CHEMICAL INTERMEDIATES SANKYO COMPANY, LIMITED (JP) 1997-03-25 US disclosed
US-5541317-A PENICILLIN DERIVATIVES, CYCLIZATION OF ESTERS OR THIOESTERS SANKYO COMPANY, LIMITED (JP) 1996-07-30 US disclosed
EP-0587436-A1 Process for preparing carbapenem and penem compounds and new compounds involved in that process SANKYO COMPANY LIMITED (JP) 1994-03-16 EP disclosed