SCHEMBL5531053

SCHEMBL5531053

CC1(C)OCCCn2c1nc(C(=O)NCc1ccc(F)cc1N1CCOC1=O)c(O)c2=O

nearest known ligand 0.41

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CYP2C9 P11712 1/20 0.41
KCNH2 Q12809 1/20 0.39
CALCA P06881 4/20 0.33
TTK P33981 1/20 0.32
KCNE1 P15382 1/20 0.32
CCR1 P32246 1/20 0.32
KCNQ1 P51787 1/20 0.32
KCNK3 O14649 1/20 0.31
MAPT P10636 1/20 0.31
ELOVL6 Q9H5J4 1/20 0.30
ALDH1A1 P00352 1/20 0.30
TSHR P16473 1/20 0.30
HSD17B10 Q99714 1/20 0.30
P2RX7 Q99572 2/20 0.30

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
SCHEMBL4043576 0.95 CYP2C9 (0.37) CYP2C9KCNH2CALCATTKKCNE1
SCHEMBL13917649 0.90 CYP2C9 (0.41) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL4830763 0.86 CYP2C9 (0.36) CYP2C9KCNH2CALCATTKKCNK3
SCHEMBL5011962 0.85 CYP2C9 (0.38) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL4036665 0.85 CYP2C9 (0.38) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL5013025 0.85 CYP2C9 (0.43) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL5015397 0.85 CYP2C9 (0.40) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL5536690 0.85 CYP2C9 (0.40) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL5620231 0.85 CYP2C9 (0.40) CYP2C9KCNH2CALCAKCNE1CCR1
SCHEMBL5013855 0.85 CYP2C9 (0.41) CYP2C9KCNH2CALCAKCNE1CCR1

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
WO-2007064316-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-06-07 WO claimed
US-7157447-B2 Bicyclic heterocycles as HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-01-02 US claimed
US-20060199956-A1 Bicyclic heterocycles as HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2006-09-07 US claimed
US-7491819-B1 N-[4-Fluorophenyl)methyl]-4,6,7,9-tetrahydro-3-hydroxy-9,9-dimethyl-4-oxo-pyrimido[2,1-c][1,4]oxazine-2-carboxamide as an HIV integrase inhibitor BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-17 US disclosed
US-7491819-B1 N-[4-Fluorophenyl)methyl]-4,6,7,9-tetrahydro-3-hydroxy-9,9-dimethyl-4-oxo-pyrimido[2,1-c][1,4]oxazine-2-carboxamide as an HIV integrase inhibitor BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-17 US disclosed
WO-2007064316-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-06-07 WO disclosed
US-7157447-B2 Bicyclic heterocycles as HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-01-02 US disclosed
US-7157447-B2 Bicyclic heterocycles as HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-01-02 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-20060199956-A1 Bicyclic heterocycles as HIV integrase inhibitors CCNI, TYMP, IMPDH1 CYP2C9 301/4885KCNH2 2366/4885CALCA 2267/4885

“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.