SCHEMBL4399776

SCHEMBL4399776

O=C(NCc1ccc(F)cc1-n1cncn1)c1nc2n(c(=O)c1O)CCN2C1CCCCC1

nearest known ligand 0.40

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CYP2C9 P11712 1/20 0.40
KCNH2 Q12809 1/20 0.37
RAB9A P51151 1/20 0.37
ACKR3 P25106 2/20 0.36
SLC22A2 O15244 8/20 0.35
HCRTR1 O43613 1/20 0.34
GPBAR1 Q8TDU6 1/20 0.34
MGLL Q99685 1/20 0.34
THRB P10828 1/20 0.33
P2RX7 Q99572 1/20 0.33
EGFR P00533 1/20 0.32

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
SCHEMBL4397223 0.84 CYP2C9 (0.37) CYP2C9KCNH2
SCHEMBL4393723 0.84 CYP2C9 (0.36) CYP2C9KCNH2SLC22A2HCRTR1P2RX7
SCHEMBL4397400 0.83 MAPK8 (0.36) CYP2C9KCNH2HCRTR1P2RX7
SCHEMBL4398133 0.82 CYP2C9 (0.36) CYP2C9KCNH2P2RX7
SCHEMBL4392728 0.82 CLPP (0.38) CYP2C9KCNH2
SCHEMBL4401303 0.82 CYP2C9 (0.36) CYP2C9KCNH2
SCHEMBL4393775 0.80 CYP2C9 (0.56) CYP2C9KCNH2RAB9ATHRB
SCHEMBL1379630 0.80 CYP2C9 (0.41) CYP2C9KCNH2HCRTR1P2RX7
SCHEMBL4832814 0.80 CYP2C9 (0.37) CYP2C9KCNH2HCRTR1
SCHEMBL4390464 0.79 KCNH2 (0.48) CYP2C9KCNH2RAB9ASLC22A2P2RX7

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
EP-1919921-B1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2012-06-27 EP claimed
US-7494984-B2 Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-24 US claimed
EP-1919921-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS Bristol-Myers Squibb Company (US) 2008-05-14 EP claimed
WO-2007027754-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-08 WO claimed
US-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2007-03-01 US claimed
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
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 CYP2C9 247/4885KCNH2 2989/4885RAB9A 4119/4885

“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.