SCHEMBL9401920

SCHEMBL9401920

CC(CN1C(=O)c2cccc3cccc(c23)C1=O)NCCNC(C)CN1C(=O)c2cccc3cccc(c23)C1=O.CS(=O)(=O)O

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
HEXA P06865 4/20 0.50
HEXB P07686 4/20 0.50
OGA O60502 1/20 0.50
CYP1B1 Q16678 1/20 0.50
SIRT1 Q96EB6 3/20 0.48
KDM4E B2RXH2 3/20 0.47
ALDH1A1 P00352 2/20 0.47
MEN1 O00255 1/20 0.47
CYP1A2 P05177 1/20 0.47
MAPT P10636 1/20 0.47
AKR1B1 P15121 1/20 0.47
HPGD P15428 1/20 0.47
ALOX15 P16050 1/20 0.47
KMT2A Q03164 1/20 0.47
HSD17B10 Q99714 1/20 0.47
LPAR2 Q9HBW0 1/20 0.44
POLB P06746 1/20 0.44
RXFP1 Q9HBX9 1/20 0.44
NPSR1 Q6W5P4 1/20 0.43

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
SCHEMBL9401924 1.00 HEXA (0.50) HEXAHEXBOGACYP1B1SIRT1
SCHEMBL9401951 0.85 FTO (0.61) CYP1B1KDM4EALDH1A1MEN1MAPT
SCHEMBL9138317 0.85 FTO (0.61) CYP1B1KDM4EALDH1A1MEN1MAPT
SCHEMBL9137157 0.85 FTO (0.61) CYP1B1KDM4EALDH1A1MEN1MAPT
SCHEMBL12660267 0.79 HEXA (0.52) HEXAHEXBOGACYP1B1SIRT1
SCHEMBL9134914 0.77 FTO (0.67) HEXAHEXBOGACYP1B1KDM4E
SCHEMBL9136054 0.77 FTO (0.67) HEXAHEXBOGACYP1B1KDM4E
SCHEMBL9134908 0.77 FTO (0.67) HEXAHEXBOGACYP1B1KDM4E
SCHEMBL12672654 0.77 HEXA (0.56) HEXAHEXBOGACYP1B1SIRT1
SCHEMBL9137315 0.77 FTO (0.67) HEXAHEXBOGACYP1B1KDM4E

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-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
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