SCHEMBL10155063

SCHEMBL10155063

c1cncc(-c2cccc3c4c([nH]c23)CCCNC4)c1

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 2/20 0.45
PARP1 P09874 2/20 0.41
CYP11B1 P15538 1/20 0.40
CYP11B2 P19099 1/20 0.40
NISCH Q9Y2I1 1/20 0.40
NPY5R Q15761 1/20 0.40
ALDH1A1 P00352 1/20 0.38
GAA P10253 1/20 0.38
APOBEC3G Q9HC16 1/20 0.38
PARP14 Q460N5 1/20 0.38
CDK4 P11802 1/20 0.38
CCND1 P24385 1/20 0.38
GFER P55789 1/20 0.37
PKN2 Q16513 1/20 0.37
PARP10 Q53GL7 1/20 0.37
PARP11 Q9NR21 1/20 0.37

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
SCHEMBL10154867 0.78 CDC7 (0.48) PARP1CYP11B1CYP11B2NPY5RCDK4
SCHEMBL10155122 0.76 SIRT2 (0.57) TAAR1CYP11B1CYP11B2
SCHEMBL620103 0.73 ACHE (0.48)
SCHEMBL1011319 0.69 PRCP (0.51) PARP1CYP11B1CYP11B2PARP10PARP11
SCHEMBL1992941 0.68 HPGDS (0.45) PARP1CYP11B1CYP11B2NPY5RCDK4
SCHEMBL148203 0.68 TDO2 (0.65) CYP11B1CYP11B2ALDH1A1PARP14
SCHEMBL29572015 0.68 TDO2 (0.65) CYP11B1CYP11B2ALDH1A1PARP14
Hydrochloric Acid SCHEMBL32663525 0.68 SIRT2 (0.65) TAAR1CYP11B1CYP11B2
SCHEMBL26259989 0.67 CYP2A6 (0.64) CYP11B1CYP11B2ALDH1A1
SCHEMBL20112107 0.67 CYP11B1 (0.46) PARP1CYP11B1CYP11B2NISCHALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120040965-A1 SUBSTITUTED AZEPINO[4,3-B]INDOLES, PHARMACOLOGICAL COMPOSITION AND A METHOD FOR THE PRODUCTION AND USE THEREOF BORISOVICH FROLOV YEVGENIY (RU) 2012-02-16 US disclosed
US-20110046368-A1 LIGANDS OF 5-HT6 RECEPTORS, A PHARMACEUTICAL COMPOSITION, METHOD FOR THE PRODUCTION AND USE THEREOF IVASHCHENKO ANDREY ALEXANDROVICH 2011-02-24 US disclosed
EP-2184064-A2 LIGANDS OF 5-HT6 RECEPTORS, A PHARMACEUTICAL COMPOSITION, METHOD FOR THE PRODUCTION AND USE THEREOF Alla Chem, LLC. (US) 2010-05-12 EP disclosed
EP-2062895-A1 SUBSTITUTED AZEPINO[4,3-B]INDOLES, PHARMACOLOGICAL COMPOSITION AND A METHOD FOR THE PRODUCTION AND USE THEREOF Alla Chem, LLC. (US) 2009-05-27 EP disclosed
WO-2008060190-A2 LIGANDS OF 5-HT6 RECEPTORS, A PHARMACEUTICAL COMPOSITION, METHOD FOR THE PRODUCTION AND USE THEREOF ALLA CHEM, LLC (US) 2008-05-22 WO disclosed
WO-2008024029-A1 SUBSTITUTED AZEPINO[4,3-B]INDOLES, PHARMACOLOGICAL COMPOSITION AND A METHOD FOR THE PRODUCTION AND USE THEREOF ALLA CHEM, LLC (US) 2008-02-28 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 (2 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-20120040965-A1 SUBSTITUTED AZEPINO[4,3-B]INDOLES, PHARMACOLOGICAL COMPOSITION AND A METHOD FOR THE PRODUCTION AND USE THEREOF ABCG2, HTR3C, AADAC TAAR1 774/4885PARP1 2055/4885CYP11B1 127/4885
US-20110046368-A1 LIGANDS OF 5-HT6 RECEPTORS, A PHARMACEUTICAL COMPOSITION, METHOD FOR THE PRODUCTION AND USE THEREOF HTR6, HTR1A, HTR3B TAAR1 98/4885PARP1 3486/4885CYP11B1 1208/4885

“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.