Guanosine

Guanosine

SCHEMBL31361372

Nc1nc2c(ncn2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1.O=P(O)(O)O.O=P(O)(O)O

nearest known ligand 0.72

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Guanosine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
NT5E P21589 2/20 0.72
HPGD P15428 1/20 0.70
TGM2 P21980 1/20 0.66
HINT1 P49773 4/20 0.64
PNP P00491 1/20 0.61
PAX8 Q06710 1/20 0.61
KRAS P01116 4/20 0.60
GSK3A P49840 2/20 0.60
RPS6KA3 P51812 2/20 0.60
MAPK14 Q16539 2/20 0.60
FUT5 Q11128 1/20 0.59
LMNA P02545 1/20 0.58
HIF1A Q16665 1/20 0.58

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
Guanosine SCHEMBL94793 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL1304255 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL376138 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL2589323 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL44407 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL8719176 0.99 NT5E (0.70) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL29220760 0.97 NT5E (0.68) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL5356557 0.97 NT5E (0.70) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL9238739 0.96 NT5E (0.69) NT5EHPGDTGM2HINT1PNP
Guanosine SCHEMBL1444901 0.96 NT5E (0.69) NT5EHPGDTGM2HINT1PNP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12251383-B2 Methods and compositions for KRAS inhibitors UNIV TEXAS (US) 2025-03-18 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-12251383-B2 Methods and compositions for KRAS inhibitors KRAS, NRAS, DHODH NT5E 1758/4885HPGD 282/4885TGM2 3442/4885

“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.