SCHEMBL7344375

SCHEMBL7344375

O=C(O)COc1cccc2cnccc12

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 5/20 0.67
ALDH1A1 P00352 2/20 0.67
HPGD P15428 2/20 0.67
TDP1 Q9NUW8 1/20 0.67
KCNA3 P22001 1/20 0.59
MAPK1 P28482 1/20 0.51
GPBAR1 Q8TDU6 1/20 0.47
MAPKAPK2 P49137 1/20 0.47
MAPT P10636 1/20 0.46
OGG1 O15527 1/20 0.46
POLB P06746 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
SUCNR1 Q9BXA5 1/20 0.45
GLA P06280 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
CASP1 P29466 1/20 0.44
HSD17B10 Q99714 1/20 0.44
NR2F2 P24468 1/20 0.44
RAB9A P51151 1/20 0.44
NR3C1 P04150 2/20 0.44

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
SCHEMBL13788236 0.87 KCNA3 (0.55) KDM4EALDH1A1HPGDTDP1KCNA3
SCHEMBL7870247 0.84 KCNA3 (0.52) KDM4EALDH1A1HPGDTDP1KCNA3
SCHEMBL3721611 0.83 KCNA3 (0.54) KDM4EALDH1A1HPGDTDP1KCNA3
SCHEMBL6999173 0.82 PDE10A (0.50) KDM4EALDH1A1KCNA3MAPK1GPBAR1
Naphthyloxyacetic Acid SCHEMBL29364154 0.80 KDM4E (1.00) KDM4EALDH1A1HPGDTDP1KCNA3
Naphthyloxyacetic Acid SCHEMBL120838 0.80 KDM4E (1.00) KDM4EALDH1A1HPGDTDP1KCNA3
SCHEMBL8546449 0.80 CASP3 (0.54) KDM4EALDH1A1HPGDTDP1KCNA3
SCHEMBL8546456 0.80 CASP3 (0.54) KDM4EALDH1A1HPGDTDP1KCNA3
Naphthyloxyacetic Acid SCHEMBL8441282 0.79 KDM4E (0.96) KDM4EALDH1A1HPGDTDP1KCNA3
Naphthyloxyacetic Acid SCHEMBL15201763 0.79 KDM4E (0.96) KDM4EALDH1A1HPGDTDP1KCNA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1990005523-A2 PHENANTHROLINEDICARBOXYLATE ESTERS, 4-AMINOQUINOLINE AND ISOQUINOLINE DERIVATIVES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE THE UPJOHN COMPANY (US) 1990-05-31 WO claimed
US-6329502-B1 VIRICIDES AGAINST HUMAN IMMUNODEFICIENCY VIRUS; TREATMENT OF AIDS (ACQUIRED IMMUNE DEFICIENCY SYNDROME) JAPAN ENERGY CORPORATION (JP) 2001-12-11 US disclosed
US-6313094-B1 COMPOSITION FOR INHIBITING HUMAN IMMUNODEFICIENCY VIRUS REPLICATION JAPAN ENERGY CORPORATION (JP) 2001-11-06 US disclosed
US-6291432-B1 (R)-N-(2-METHYLBENZYL)-3-((2S, 3S)-3-(N-(2-CHROMONECARBONYL)-L-ASPARAGINYL)AMINO-2-HYDROXY-4-PHENYLBUTANO YL)-5,5-DIMETHYL-1,3-THIAZOLIDINE-4-CARBOXAMIDE CAN BE GIVEN AS A TYPICAL EXAMPLE OF THIS COMPOUND. JAPAN ENERGY CORPORATION (JP) 2001-09-18 US disclosed
EP-0490667-B1 HIV protease inhibitors JAPAN ENERGY CORP (JP) 1999-06-09 EP disclosed
EP-0900566-A1 NOVEL TRIPEPTIDE COMPOUNDS AND ANTI-AIDS DRUGS JAPAN ENERGY CORPORATION (JP) 1999-03-10 EP disclosed
EP-0574135-B1 Process for producing peptide derivatives and salts thereof JAPAN ENERGY CORP (JP) 1998-11-18 EP disclosed
EP-0812839-A1 Irreversible HIV protease inhibitors, compositions containing same and process for the preparation thereof LG Chemical Limited (KR) 1997-12-17 EP disclosed
EP-0812857-A1 Irreversible HIV protease inhibitors, compositions containing same and process for the preparation thereof LG Chemical Limited (KR) 1997-12-17 EP disclosed
US-5679687-A Irreversible HIV protease inhibitors, compositions containing same and process for the preparation thereof LG CHEMICAL LIMITED (KR) 1997-10-21 US disclosed
US-5670517-A MULTISTAGE SYNTHESIS WITH EPOXIDATION, DECARBONYLATION, COUPLING BY AMIDATION THEN DECARBONYLATION LG CHEMICAL LIMITED (KR) 1997-09-23 US disclosed
US-5644028-A Process for producing peptide derivatives and salts therefor JAPAN ENERGY CORPORATION (JP) 1997-07-01 US disclosed
EP-0574135-A1 Process for producing peptide derivatives and salts thereof JAPAN ENERGY CORPORATION (JP) 1993-12-15 EP disclosed
EP-0490667-A2 HIV protease inhibitors JAPAN ENERGY CORPORATION (JP) 1992-06-17 EP disclosed
WO-1990005523-A2 PHENANTHROLINEDICARBOXYLATE ESTERS, 4-AMINOQUINOLINE AND ISOQUINOLINE DERIVATIVES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE THE UPJOHN COMPANY (US) 1990-05-31 WO disclosed