SCHEMBL10372389

SCHEMBL10372389

CCCCCC1=Nc2cnccc2Nc2ccccc21

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.40
▸ TDP1 Q9NUW8 1/20 0.40
▸ GAA P10253 1/20 0.36
▸ MAPT P10636 1/20 0.36
▸ IDO1 P14902 1/20 0.36
▸ PDE5A O76074 1/20 0.35
▸ DRD2 P14416 2/20 0.33
▸ DRD4 P21917 1/20 0.33
▸ CDK2 P24941 3/20 0.33
▸ CCNT1 O60563 1/20 0.33
▸ CCNT2 O60583 1/20 0.33
▸ CCNB2 O95067 1/20 0.33
▸ CDK1 P06493 1/20 0.33
▸ CCNB1 P14635 1/20 0.33
▸ CCNA2 P20248 1/20 0.33
▸ CDK9 P50750 1/20 0.33
▸ CCNA1 P78396 1/20 0.33
▸ CDK5 Q00535 1/20 0.33
▸ CDK5R1 Q15078 1/20 0.33
▸ CCNB3 Q8WWL7 1/20 0.33

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
SCHEMBL10373566 0.78 CYP1A2 (0.40) DRD2DRD4
SCHEMBL10373749 0.73 GAA (0.52) L3MBTL1GAAMAPTIDO1CDK2
SCHEMBL2506350 0.73 MAPT (0.42) L3MBTL1TDP1GAAMAPTIDO1
Hydrochloric Acid SCHEMBL11063449 0.69 TDP1 (0.43) L3MBTL1TDP1PPARA
Hydrochloric Acid SCHEMBL11069551 0.69 TDP1 (0.43) L3MBTL1TDP1PPARA
Hydrochloric Acid SCHEMBL11063453 0.69 TDP1 (0.43) L3MBTL1TDP1PPARA
SCHEMBL2364518 0.68 GABRA1 (0.54) CCNB2CDK1CCNB1CCNB3CCKAR
SCHEMBL6157468 0.66 MEN1 (0.45) GAAMAPTCCNB2CDK1CCNB1
SCHEMBL6159010 0.66 MEN1 (0.45) GAAMAPTCCNB2CDK1CCNB1
SCHEMBL7572055 0.65 GPR3 (0.35) L3MBTL1TDP1GPR3LIPG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0076017-B1 PHENYL SUBSTITUTED PYRIDO(1,4)BENZODIAZEPINES AND INTERMEDIATES THEREFOR A.H. ROBINS COMPANY, INCORPORATED (US) 1990-08-16 — — EP claimed
EP-0076017-A2 Phenyl substituted pyrido(1,4)benzodiazepines and intermediates therefor A.H. ROBINS COMPANY, INCORPORATED (US) 1983-04-06 — — EP claimed
EP-0076017-B1 PHENYL SUBSTITUTED PYRIDO(1,4)BENZODIAZEPINES AND INTERMEDIATES THEREFOR A.H. ROBINS COMPANY, INCORPORATED (US) 1990-08-16 — — EP disclosed
EP-0107261-B1 (2-((NITROPYRIDINYL)AMINO)PHENYL)ARYLMETHANONES AND SALTS, THEIR USE IN MEDICINE, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR USE IN THE PREPARATION OF (2-((AMINOPYRIDINYL)AMINO)PHENYL)ARYLMETHANONES AND PYRIDO(1,4)BENZODIAZEPINES A.H. ROBINS COMPANY, INCORPORATED (US) 1988-09-21 — — EP disclosed
US-4698430-A ANTIDEPRESSANT A. H. ROBINS COMPANY, INC. (US) 1987-10-06 — — US disclosed
US-4668675-A ANTIDEPRESSANTS A. H. ROBINS COMPANY, INCORPORATED (US) 1987-05-26 — — US disclosed
US-4628100-A ANTIDEPRESSANTS A. H. ROBINS COMPANY, INCORPORATED (US) 1986-12-09 — — US disclosed
US-4560510-A CONDENSATION OF AN AMINOCHLOROPYRIDINE WITH A ARYL(AMINOPHENYL)METHANONE WITH A BASE) A. H. ROBINS COMPANY, INCORPORATED (US) 1985-12-24 — — US disclosed
US-4558132-A ANTIDEPRESSANTS A. H. ROBINS COMPANY, INCORPORATED (US) 1985-12-10 — — US disclosed
US-4556667-A (2-((AMINOPYRIDINYL)AMINO)PHENYL)ARYLMETHANONE INTERMEDIATES A. H. ROBINS COMPANY, INCORPORATED (US) 1985-12-03 — — US disclosed
EP-0157656-A2 Process and intermediates for the preparation of aryl substituded pyrido [1,4] benzodiazepines A.H. ROBINS COMPANY, INCORPORATED (US) 1985-10-09 — — EP disclosed
US-4518603-A ANTIDEPRESSANTS A. H. ROBINS COMPANY, INC. (US) 1985-05-21 — — US disclosed
US-4495183-A ANTIULCER AGENTS- GASTROLINTESTINAL DISORDERS A. H. ROBINS COMPANY, INCORPORATED (US) 1985-01-22 — — US disclosed
US-4480100-A CHEMICAL INTERMEDIATES FOR ANTIDEPRESSANTS A. H. ROBINS COMPANY, INC. (US) 1984-10-30 — — US disclosed
US-4447361-A ANTIDEPRESSANT A. H. ROBINS COMPANY, INC. (US) 1984-05-08 — — US disclosed
EP-0107261-A2 (2-((Nitropyridinyl)amino)phenyl)arylmethanones and salts, their use in medicine, pharmaceutical compositions containing them and their use in the preparation of (2-((aminopyridinyl)amino)phenyl)arylmethanones and pyrido(1,4)benzodiazepines A.H. ROBINS COMPANY, INCORPORATED (US) 1984-05-02 — — EP disclosed
EP-0099614-A2 Nitro, amino and aroylamino-N-phenylpyridinamines and their use in a process for preparing pyrido(1,4)benzodiazapines A.H. ROBINS COMPANY, INCORPORATED (US) 1984-02-01 — — EP disclosed
EP-0076017-A2 Phenyl substituted pyrido(1,4)benzodiazepines and intermediates therefor A.H. ROBINS COMPANY, INCORPORATED (US) 1983-04-06 — — EP disclosed
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