SCHEMBL17359519

SCHEMBL17359519

C#C[C@@]1(n2cnc3c(=O)[nH]c(N)nc32)O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O

nearest known ligand 0.51

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
POLG P54098 2/20 0.51
TGM2 P21980 1/20 0.51
PNP P00491 1/20 0.49
KRAS P01116 2/20 0.48
FUT5 Q11128 1/20 0.48
POLB P06746 3/20 0.48
P2RY6 Q15077 2/20 0.47
P2RY2 P41231 1/20 0.47
P2RY4 P51582 1/20 0.47
NT5E P21589 1/20 0.46
POLA1 P09884 1/20 0.44
P2RX3 P56373 4/20 0.44
DCPS Q96C86 1/20 0.42
P2RX1 P51575 3/20 0.41
P2RX2 Q9UBL9 1/20 0.41
P2RX4 Q99571 2/20 0.41
ENPP1 P22413 1/20 0.41
P2RY1 P47900 1/20 0.41
P2RY11 Q96G91 1/20 0.41

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
SCHEMBL16647568 0.94 TGM2 (0.49) POLGTGM2PNPKRASFUT5
SCHEMBL16368348 0.94 TGM2 (0.49) POLGTGM2PNPKRASFUT5
SCHEMBL17357557 0.90 IMPDH2 (0.42) POLGTGM2PNPKRASFUT5
SCHEMBL4410921 0.87 TGM2 (0.55) POLGTGM2PNPKRASFUT5
SCHEMBL4076696 0.86 POLG (0.53) POLGTGM2PNPKRASFUT5
SCHEMBL4381958 0.86 POLG (0.53) POLGTGM2PNPKRASFUT5
SCHEMBL309062 0.85 TGM2 (0.53) POLGTGM2PNPKRASFUT5
SCHEMBL401417 0.85 TGM2 (0.53) POLGTGM2PNPKRASFUT5
SCHEMBL30301189 0.85 TGM2 (0.53) POLGTGM2PNPKRASFUT5
SCHEMBL8435629 0.85 POLG (0.51) POLGTGM2PNPKRASFUT5

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
CN-119431453-A Phosphorus (V) based reagent, method for the production thereof, and use thereof for producing stereoregular organic phosphorus (V) compounds 百时美施贵宝公司 2025-02-14 CN disclosed
US-10307439-B2 Substituted nucleosides, nucleotides and analogs thereof ALIOS BIOPHARMA, INC. (US) 2019-06-04 US disclosed
US-20170143749-A1 SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF Janssen Biopharma, Inc. 2017-05-25 US disclosed
US-20170143749-A1 SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF Janssen Biopharma, Inc. 2017-05-25 US disclosed
US-20150366888-A1 SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF Janssen Pharmaceuticals, Inc. 2015-12-24 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 (3 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-10307439-B2 Substituted nucleosides, nucleotides and analogs thereof PNP, NT5C3B, TYMP POLG 956/4885TGM2 938/4885PNP 1/4885
US-20150366888-A1 SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF PNP, NT5C3B, TYMP POLG 956/4885TGM2 938/4885PNP 1/4885
US-20170143749-A1 SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF PNP, NT5C3B, TYMP POLG 956/4885TGM2 938/4885PNP 1/4885

“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.