Bisnafide

Bisnafide

SCHEMBL9136352

CS(=O)(=O)O.C[C@H](CNCCNC[C@@H](C)N1C(=O)c2cccc3cc([N+](=O)[O-])cc(c23)C1=O)N1C(=O)c2cccc3cc([N+](=O)[O-])cc(c23)C1=O

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Bisnafide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MCL1 known ✓ Q07820 1/20 0.44
FTO Q9C0B1 2/20 0.56
NTRK1 P04629 1/20 0.56
NGFR P08138 1/20 0.56
PABPC1 P11940 2/20 0.51
CA12 O43570 3/20 0.50
CA1 P00915 3/20 0.50
CA2 P00918 3/20 0.50
CA9 Q16790 3/20 0.50
MEN1 O00255 6/20 0.49
KMT2A Q03164 6/20 0.49
POLB P06746 5/20 0.48
TDP1 Q9NUW8 1/20 0.48
MAPT P10636 3/20 0.48
KDM4E B2RXH2 2/20 0.48
S1PR1 P21453 1/20 0.48
HTT P42858 1/20 0.48
RAD52 P43351 1/20 0.48
RECQL P46063 1/20 0.48
RAB9A P51151 1/20 0.48

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
Bisnafide SCHEMBL9136711 1.00 FTO (0.56) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL3726 1.00 FTO (0.56) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL9401929 1.00 FTO (0.56) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL9135842 1.00 FTO (0.56) FTONTRK1NGFRPABPC1CA12
SCHEMBL9348432 0.99 FTO (0.55) FTONTRK1NGFRPABPC1CA12
SCHEMBL9352147 0.99 FTO (0.55) FTONTRK1NGFRPABPC1CA12
SCHEMBL9349753 0.99 FTO (0.55) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL9136305 0.95 FTO (0.61) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL9135739 0.95 FTO (0.61) FTONTRK1NGFRPABPC1CA12
Bisnafide SCHEMBL9136683 0.95 FTO (0.61) FTONTRK1NGFRPABPC1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5461176-A Reacting alanine methyl ester with oxalyl chloride, treating with ammonia in methanol, reducing amides with diborane in tetrahydrofuran, neutralizing with sodium ethoxide to yield free amine THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1995-10-24 US disclosed
US-5329048-A Reaction of tert-butyloxycarbonylaniline with 1,1' carbonyl diimidazole then ethylenediamine, then acidification to remove tert-butyloxycarbonyl THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1994-07-12 US disclosed
EP-0577753-A1 BIS-NAPHTHALIMIDES CONTAINING AMINO-ACID DERIVED LINKERS AS ANTICANCER AGENTS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1994-01-12 EP disclosed
US-5206249-A Diastereoisomers; enantiomorphs; antitumor agents DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1993-04-27 US disclosed
WO-1992017453-A1 BIS-NAPHTHALIMIDES CONTAINING AMINO-ACID DERIVED LINKERS AS ANTICANCER AGENTS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1992-10-15 WO disclosed
EP-0506008-A1 Bis-naphthalimides containing amino-acid derived linkers as anticancer agents THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1992-09-30 EP disclosed