SCHEMBL5665238

SCHEMBL5665238

C[C@H]1C[C@@]1(Cn1cnc2c(N)ncnc21)OCP(=O)(O)O

nearest known ligand 0.56

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
FGFR1 P11362 2/20 0.56
SLC22A6 Q4U2R8 1/20 0.56
CYP3A4 P08684 4/20 0.56
ENPP1 P22413 1/20 0.47
ADORA2A P29274 4/20 0.45
ADORA1 P30542 4/20 0.45
PI4KA P42356 1/20 0.45
PI4K2B Q8TCG2 1/20 0.45
PI4K2A Q9BTU6 1/20 0.45
PI4KB Q9UBF8 1/20 0.45
METTL3 Q86U44 1/20 0.44
METTL14 Q9HCE5 1/20 0.44
P2RY1 P47900 1/20 0.43
ADORA2B P29275 1/20 0.43
CYP2D6 P10635 3/20 0.43
AHCY P23526 1/20 0.43

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
SCHEMBL3293448 1.00 FGFR1 (0.56) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL6054011 0.89 FGFR1 (0.53) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL5662571 0.89 FGFR1 (0.53) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL6053615 0.87 FGFR1 (0.52) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL6053630 0.87 FGFR1 (0.52) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL3294539 0.86 CDK1 (0.46) FGFR1SLC22A6CYP3A4ENPP1AHCY
SCHEMBL13328630 0.86 CYP3A4 (0.48) FGFR1SLC22A6CYP3A4ADORA2AADORA1
SCHEMBL4279921 0.84 CYP3A4 (0.47) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL4279920 0.84 ADORA2A (0.48) FGFR1SLC22A6CYP3A4ENPP1ADORA2A
SCHEMBL2904496 0.82 FGFR1 (0.61) FGFR1SLC22A6CYP3A4ENPP1ADORA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1546164-A4 (+)-TRANS-ISOMERS OF (1-PHOSPHONOMETHOXY-2-ALKYLCYCLOPROPYL) METHYL NUCLEOSIDE DERIVATIVES, PROCESS FOR THE PREPARATION OF STEREOISOMERS THEREOF, AND USE OF ANTIVIRAL AGENTS THEREOF LG LIFE SCIENCES LTD (KR) 2006-06-07 EP disclosed
US-20060111324-A1 (+)-Ttrans-isomers of (1-phosphonomethoxy-2-alkylcyclopropyl)methyl nucleoside derivatives, process for the preparation of stereoisomers thereof, and use of antiviral agents thereof LG LIFE SCIENCES (KR) 2006-05-25 US disclosed
EP-1546164-A1 (+)-TRANS-ISOMERS OF (1-PHOSPHONOMETHOXY-2-ALKYLCYCLOPROPYL) METHYL NUCLEOSIDE DERIVATIVES, PROCESS FOR THE PREPARATION OF STEREOISOMERS THEREOF, AND USE OF ANTIVIRAL AGENTS THEREOF LG Life Sciences Ltd. (KR) 2005-06-29 EP disclosed
WO-2004029064-A1 (+)-TRANS-ISOMERS OF (1-PHOSPHONOMETHOXY-2-ALKYLCYCLOPROPYL) METHYL NUCLEOSIDE DERIVATIVES, PROCESS FOR THE PREPARATION OF STEREOISOMERS THEREOF, AND USE OF ANTIVIRAL AGENTS THEREOF LG LIFE SCIENCES LTD. (KR) 2004-04-08 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 (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-20060111324-A1 (+)-Ttrans-isomers of (1-phosphonomethoxy-2-alkylcyclopropyl)methyl nucleoside derivatives, process for the preparation of stereoisomers thereof, and use of antiviral agents thereof TTR, HAVCR2, PNP FGFR1 2540/4885SLC22A6 1606/4885CYP3A4 580/4885

“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.