SCHEMBL13243791

SCHEMBL13243791

Cn1c(C2CCOCC2)nc(C(=O)NCc2ccc(F)cc2N2CCCCS2(=O)=O)c(O)c1=O

nearest known ligand 0.46

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CALCA P06881 13/20 0.46
CYP2C9 P11712 1/20 0.41
KCNH2 Q12809 1/20 0.38
P2RX7 Q99572 3/20 0.36
AADAT Q8N5Z0 1/20 0.35
KCNE1 P15382 1/20 0.34
CCR1 P32246 1/20 0.34
KCNQ1 P51787 1/20 0.34

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
SCHEMBL13243788 0.96 CALCA (0.45) CALCACYP2C9KCNH2P2RX7KCNE1
SCHEMBL2967365 0.94 CALCA (0.41) CALCACYP2C9KCNH2P2RX7AADAT
SCHEMBL2957301 0.90 CALCA (0.40) CALCACYP2C9KCNH2P2RX7
SCHEMBL13243792 0.89 CALCA (0.44) CALCACYP2C9KCNH2AADAT
SCHEMBL13243787 0.85 CALCA (0.43) CALCACYP2C9KCNH2AADAT
SCHEMBL2962478 0.84 CALCA (0.39) CALCACYP2C9AADAT
SCHEMBL2965986 0.81 CYP2C9 (0.38) CYP2C9KCNH2P2RX7AADATKCNE1
SCHEMBL2967109 0.81 CYP2C9 (0.37) CYP2C9KCNH2P2RX7AADATKCNE1
SCHEMBL2957321 0.81 KCNE1 (0.38) CYP2C9KCNH2P2RX7AADATKCNE1
SCHEMBL5015342 0.80 CALCA (0.47) CALCACYP2C9KCNH2P2RX7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7763630-B2 pyrimidinone compounds such as N-(4-Fluorobenzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide, used for treating human immunodeficiency virus (HIV) and acquired immune deficiency syndrome (AIDS) BRISTOL-MYERS SQUIBB COMPANY (US) 2010-07-27 US disclosed
US-7763630-B2 pyrimidinone compounds such as N-(4-Fluorobenzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide, used for treating human immunodeficiency virus (HIV) and acquired immune deficiency syndrome (AIDS) BRISTOL-MYERS SQUIBB COMPANY (US) 2010-07-27 US disclosed
WO-2008154246-A1 HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2008-12-18 WO disclosed
US-20080306051-A1 HIV Integrase Inhibitors BRISTOL-MYERS SQUIBB COMPANY 2008-12-11 US disclosed
US-20080306051-A1 HIV Integrase Inhibitors BRISTOL-MYERS SQUIBB COMPANY 2008-12-11 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-20080306051-A1 HIV Integrase Inhibitors TYMP, IMPDH1, UNG CALCA 2954/4885CYP2C9 655/4885KCNH2 3016/4885

“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.