Guanosine

Guanosine

SCHEMBL44407

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.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 SCHEMBL31361372 1.00 NT5E (0.72) NT5EHPGDTGM2HINT1PNP
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 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

Appears in 15320 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4747627-A1 METHODS AND SYSTEMS FOR PREDICTIVE CLASSIFICATION BY MASS SPECTROMETRY AND TRAINED LARGE SPECTRAL MODELS Matterworks Inc (US) 2026-05-27 EP claimed
WO-2026098772-A1 SINGLE-POT IN VITRO TRANSCRIPTION OF SYNTHETIC CAPPED MRNA ANEMOCYTE S.R.L. (IT) 2026-05-15 WO claimed
WO-2026099317-A2 SINGLE-POT IN VITRO TRANSCRIPTION OF SYNTHETIC CAPPED MRNA ANEMOCYTE S.R.L. (IT) 2026-05-15 WO claimed
EP-3869192-B1 METHOD FOR QUANTITATIVE DETECTION OF VARIOUS METABOLITES IN BIOLOGICAL SAMPLE HUMAN METABOLOMICS INST INC (CN) 2026-05-13 EP claimed
US-20260117271-A1 SPECTRAL MONITORING OF IN VITRO TRANSCRIPTION SANOFI PASTEUR INC (US) 2026-04-30 US claimed
EP-4722361-A1 VECTOR USED FOR PREPARING CIRCULAR RNA AND METHOD Nanjing GenScript Biotech Co., Ltd. (CN) 2026-04-08 EP claimed
US-20260076917-A1 COMPOSITION AND PROCESS FOR A LIPID NANO-PARTICLE DELIVERY OF OXYGEN AND VITAL METABOLIC COMPOUNDS FOR HEMORRHAGIC SHOCK KALOCYTE INC (US) 2026-03-19 US claimed
US-20260072030-A1 RAS BIOSENSORS UNIV CALIFORNIA (US) 2026-03-12 US claimed
US-20260062439-A1 Enzymatic RNA Capping Method NEW ENGLAND BIOLABS, INC. (US) 2026-03-05 US claimed
US-20260062438-A1 Enzymatic RNA Capping Method NEW ENGLAND BIOLABS, INC. (US) 2026-03-05 US claimed
WO-1991014699-A1 SITE SPECIFIC CLEAVAGE OF SINGLE-STRANDED DNA THE UNIVERSITY OF COLORADO FOUNDATION, INC. (US) 1991-10-03 WO claimed
WO-1990010234-A1 METHOD AND KIT FOR DETERMINING TYROSINE-PHOSPHORYLATING AND DEPHOSPHORYLATING ACTIVITIES EURO-DIAGNOSTICS B.V. (NL) 1990-09-07 WO claimed
US-4826824-A Method of enhancing the taste perception of sweetness of aspartame and derivatives thereof DUKE UNIVERSITY (US) 1989-05-02 US claimed
US-4806415-A COLORIMETRIC ANALYSIS OF GENERATED ENZYME MILES INC. (US) 1989-02-21 US claimed
US-4575498-A 5-AMINO-4-IMIDAZOLE CARBOXAMIDE RIBOSIDE DUKE UNIVERSITY (US) 1986-03-11 US claimed
EP-0073628-B1 LIGHT-SENSITIVE COMPOSITIONS USING RHODOPSIN AND LIGHT-ACTIVATABLE ENZYMES EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1985-02-20 EP claimed
EP-0073628-A1 Light-sensitive compositions using rhodopsin and light-activatable enzymes EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1983-03-09 EP claimed
US-4356256-A Photographic compositions, elements and processes using light-activatable enzymes EASTMAN KODAK CO. (US) 1982-10-26 US claimed
US-4318980-A Heterogenous specific binding assay employing a cycling reactant as label MILES LABORATORIES, INC. (US) 1982-03-09 US claimed
US-4046879-A TOPICAL BOEHRINGER INGELHEIM GMBH (DT) 1977-09-06 US claimed