SCHEMBL4397014

SCHEMBL4397014

CCCCN1CCn2c1nc(C(=O)NCc1ccc(F)cc1S(=O)(=O)N(C)C)c(OCc1ccccc1)c2=O

nearest known ligand 0.35

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ADORA3 P0DMS8 1/20 0.35
ADORA2B P29275 1/20 0.35
KCNH2 Q12809 1/20 0.33
KDM1A O60341 1/20 0.32
TRPV1 Q8NER1 1/20 0.32
CNR2 P34972 3/20 0.32
CNR1 P21554 2/20 0.32
KDM4E B2RXH2 1/20 0.32
ALDH1A1 P00352 1/20 0.32
SCD O00767 1/20 0.31
HTR7 P34969 1/20 0.31

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
SCHEMBL10077173 0.88 KCNH2 (0.34) KCNH2TRPV1KDM4EALDH1A1SCD
SCHEMBL4390329 0.87 TRPV1 (0.35) KCNH2TRPV1KDM4EALDH1A1
SCHEMBL4390455 0.87 ADORA3 (0.37) ADORA3ADORA2BCNR2CNR1SCD
SCHEMBL4393819 0.86 KCNH2 (0.43) KCNH2ALDH1A1
SCHEMBL4393779 0.85 ADORA3 (0.45) ADORA3ADORA2BCNR2CNR1KDM4E
SCHEMBL4397739 0.83 CNR1 (0.35) ADORA3ADORA2BCNR2CNR1SCD
SCHEMBL4035378 0.81 KCNH2 (0.38) KCNH2KDM4EALDH1A1
SCHEMBL4394467 0.80 ADORA3 (0.41) ADORA3ADORA2BCNR2CNR1KDM4E
SCHEMBL4397731 0.79 KCNH2 (0.43) KCNH2
SCHEMBL4391905 0.78 SCD (0.41) KDM4EALDH1A1SCD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1919921-B1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2012-06-27 EP disclosed
US-7494984-B2 Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-24 US disclosed
US-7494984-B2 Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-24 US disclosed
EP-1919921-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS Bristol-Myers Squibb Company (US) 2008-05-14 EP disclosed
WO-2007027754-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-08 WO disclosed
WO-2007027754-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-08 WO disclosed
US-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2007-03-01 US disclosed
US-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2007-03-01 US 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-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors CCNI, APOBEC3C, CDKN1A ADORA3 1274/4885ADORA2B 2651/4885KCNH2 2989/4885

“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.