SCHEMBL6474512

SCHEMBL6474512

[c]1cc(-c2cccnc2)on1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 13/20 0.50
CYP3A4 P08684 6/20 0.50
ALDH1A1 P00352 3/20 0.50
CYP1A2 P05177 1/20 0.50
CYP2C19 P33261 6/20 0.44
CYP2D6 P10635 5/20 0.44
CYP2C9 P11712 5/20 0.44
CYP2E1 P05181 4/20 0.44
CYP2B6 P20813 4/20 0.44
KDM4E B2RXH2 2/20 0.44
TP53 P04637 2/20 0.44
HPGD P15428 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
HSD17B10 Q99714 2/20 0.44
LMNA P02545 1/20 0.44
MAPT P10636 1/20 0.44
ALOX15 P16050 1/20 0.44
HTT P42858 1/20 0.44
CHRNB2 P17787 1/20 0.43
CHRNA5 P30532 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
SCHEMBL2462291 0.72 CYP2A6 (0.52) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL2725990 0.71 PTK2 (0.61) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL5162459 0.71 CYP2A6 (0.56) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL21295701 0.70 CYP2A6 (0.50) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL120088 0.70 CYP2A6 (1.00) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL30473120 0.70 CYP2A6 (1.00) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL29419014 0.70 CYP2A6 (1.00) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
SCHEMBL2492199 0.69 TDO2 (0.42) TP53SMN1; SMN2TDO2NPC1RAB9A
SCHEMBL4569991 0.68 CYP2A6 (0.52) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19
Hydrochloric Acid SCHEMBL4831090 0.67 CYP2A6 (0.94) CYP2A6CYP3A4ALDH1A1CYP1A2CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6900209-B2 Nitrogen substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives for enhancing cognition MERCK SHARP & DOHME LTD. 2005-05-31 US disclosed
US-20040043982-A1 Nitrogen substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives for enhancing cognition MERCK SHARP & DOHME LTD. (GB) 2004-03-04 US disclosed
US-6613766-B1 Compounds such as 3-(5-methylisoxazol-3-yl)-5-(2-pyridyl-methyloxy)-1,2,3a,4,6 -pentaazacyclopenta(a)naphthalene, having high receptivity for the inhibitory neurotransmitter, gamma-aminobutyric acid (GABA); learning enhancement MERCK SHARP & DOHME LTD. 2003-09-02 US disclosed
EP-0986562-B1 SUBSTITUTED 1,2,4-TRIAZOLO 3,4-A]PHTHALAZINE DERIVATIVES AS GABA ALPHA 5 LIGANDS MERCK SHARP & DOHME (GB) 2002-08-07 EP disclosed
US-6310203-B1 Precursor compounds to substituted 1,2,4-triazolo[3,4,-a]phathalazine GABA alpha 5 ligands MERCK SHARPE & DOHME LIMITED (GB) 2001-10-30 US disclosed
EP-1129090-A1 PENTAAZA-CYCLOPENTA A]NAPHTHALENE DERIVATIVES AS LIGANDS FOR GABA A? $g(a)5 RECEPTORS MERCK SHARP & DOHME LTD. (GB) 2001-09-05 EP disclosed
US-6200975-B1 FOR COGNITION ENHANCEMENT THERAPY MERCK SHARP & DOHME LIMITED (GB) 2001-03-13 US disclosed
WO-2000029412-A1 PENTAAZA-CYCLOPENTA[A]NAPHTHALENE DERIVATIVES AS LIGANDS FOR GABAA α5 RECEPTORS MERCK SHARP & DOHME LIMITED (GB) 2000-05-25 WO disclosed
EP-0986562-A1 SUBSTITUTED 1,2,4-TRIAZOLO 3,4-A]PHTHALAZINE DERIVATIVES AS GABA ALPHA 5 LIGANDS MERCK SHARP & DOHME LTD. (GB) 2000-03-22 EP disclosed
WO-1998050385-A1 SUBSTITUTED 1,2,4-TRIAZOLO[3,4-a]PHTHALAZINE DERIVATIVES AS GABA ALPHA 5 LIGANDS MERCK SHARP & DOHME LIMITED (GB) 1998-11-12 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040043982-A1 Nitrogen substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives for enhancing cognition PSEN1, BDNF, H1-5 CYP2A6 2808/4885CYP3A4 2494/4885ALDH1A1 2928/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.