Benzidine

Benzidine

SCHEMBL3908661

Nc1ccc(-c2ccc(N)cc2)cc1.Nc1ccc(-c2ccc(N)cc2)cc1.Nc1ccc(-c2ccc(N)cc2)cc1.Nc1ccc(-c2ccc(N)cc2)cc1.S.S

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP3A4 P08684 7/20 0.92
▸ ALDH1A1 P00352 7/20 0.92
▸ TDP1 Q9NUW8 5/20 0.92
▸ TP53 P04637 2/20 0.92
▸ HSD17B10 Q99714 4/20 0.69
▸ TAAR1 Q96RJ0 2/20 0.69
▸ MAPT P10636 4/20 0.67
▸ MEN1 O00255 3/20 0.67
▸ KMT2A Q03164 3/20 0.67
▸ KIF11 P52732 1/20 0.55
▸ APP P05067 2/20 0.53
▸ NPC1 O15118 4/20 0.52
▸ RAB9A P51151 4/20 0.52
▸ SMN1; SMN2 Q16637 3/20 0.52
▸ CA14 Q9ULX7 2/20 0.52
▸ KDM4E B2RXH2 2/20 0.52
▸ HPGD P15428 2/20 0.52
▸ CA12 O43570 1/20 0.52
▸ CA1 P00915 1/20 0.52
▸ CA2 P00918 1/20 0.52

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
Benzidine SCHEMBL16009789 1.00 CYP3A4 (0.92) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL10697986 0.96 CYP3A4 (0.85) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL22129123 0.96 CYP3A4 (0.85) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL720393 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
SCHEMBL2024128 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
SCHEMBL28842081 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL29021 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL5140469 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
SCHEMBL258287 0.96 CYP3A4 (1.00) CYP3A4ALDH1A1TDP1TP53HSD17B10
Benzidine SCHEMBL25274606 0.92 CYP3A4 (0.92) CYP3A4ALDH1A1TDP1TP53HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7572828-B2 contacting a nucleocapsid protein of the virus with a antimonyphenyl cpompound containin at least one carboxy, carboxy ester or amide group for inhibiting retroviral replication THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2009-08-11 — — US disclosed
EP-1575549-A4 IDENTIFICATION OF ANTI-HIV COMPOUNDS INHIBITING VIRUS ASSEMBLY AND BINDING OF NUCLEOCAPSID PROTEIN TO NUCLEIC ACID US GOV HEALTH & HUMAN SERV (US) 2008-05-07 — — EP disclosed
US-20060263772-A1 Identification of anti-hiv compounds inhibiting virus assembly and binding of nucleocapsid protein to nucleic acid THE GOVERNMENT OF THE USA AS REPRESENTED BY THE SECRETARY OF THE DEPT. OF HEALTH AND HUMAN SERVICE (US) 2006-11-23 — — US disclosed
EP-1575549-A2 IDENTIFICATION OF ANTI-HIV COMPOUNDS INHIBITING VIRUS ASSEMBLY AND BINDING OF NUCLEOCAPSID PROTEIN TO NUCLEIC ACID The Government of the USA as represented by the Secretary of the Dept. of Health ahd Human services (US) 2005-09-21 — — EP disclosed
WO-2004032869-A2 IDENTIFICATION OF ANTI-HIV COMPOUNDS INHIBITING VIRUS ASSEMBLY AND BINDING OF NUCLEOCAPSID PROTEIN TO NUCLEIC ACID THE GOVERNMENT OF THE USA AS REPRESENTED BY THE SECRETARY OF THE DEPT. OF HEALTH AND HUMAN SERVICES (US) 2004-04-22 — — WO disclosed
WO-2002062333-A9 USE OF 9H-XANTHENES IN A METHOD OF INHIBITING VIRAL REPLICATION TARGETING THE NUCLEOCAPSID PROTEIN US GOV HEALTH & HUMAN SERV (US) 2003-01-30 — — WO disclosed
WO-2002062333-A1 USE OF 9H-XANTHENES IN A METHOD OF INHIBITING VIRAL REPLICATION TARGETING THE NUCLEOCAPSID PROTEIN THE GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2002-08-15 — — WO disclosed
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