Deoxyuridine

Deoxyuridine

SCHEMBL16633412

O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)OP(=O)(O)O.O=c1ccn(C2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]1.O=c1ccn(C2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]1

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ADRA1A known ✓ P35348 1/20 0.50
DUT P33316 4/20 0.68
P2RY2 P41231 4/20 0.53
P2RY6 Q15077 3/20 0.53
LMNA P02545 2/20 0.53
SMN1; SMN2 Q16637 2/20 0.53
TK1 P04183 2/20 0.53
SLC28A1 O00337 1/20 0.51
SLC28A2 O43868 1/20 0.51
SLC29A1 Q99808 1/20 0.51
SLC28A3 Q9HAS3 1/20 0.51
P2RY4 P51582 2/20 0.51
ALOX12 P18054 1/20 0.50
TK2 O00142 1/20 0.49
TYMS P04818 1/20 0.48

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
Deoxyuridine SCHEMBL156693 0.99 DUT (0.70) DUTP2RY2P2RY6LMNASMN1; SMN2
Deoxyuridine SCHEMBL1501332 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL157130 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL20585969 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL27615744 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL3709892 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL15199 0.95 DUT (0.64) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL6066345 0.94 DUT (0.67) DUTP2RY2P2RY6LMNASMN1; SMN2
Deoxyuridine SCHEMBL3961108 0.94 DUT (0.63) DUTLMNASMN1; SMN2TK1SLC28A1
Deoxyuridine SCHEMBL20585970 0.94 DUT (0.66) DUTP2RY2P2RY6P2RY4

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
WO-2016168735-A1 NUCLEOSIDE SUPPLEMENTATION TO PROMOTE CELLULAR FUNCTION, GENETIC STABILITY AND AUGMENT TRANSGENIC EXPRESSION THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2016-10-20 WO disclosed
EP-3058061-A1 NUCLEOSIDE SUPPLEMENTATION TO PROMOTE CELLULAR FUNCTION, GENETIC STABILITY AND REGENERATIVE APPLICATIONS The Regents of the University of California (US) 2016-08-24 EP disclosed
WO-2015057997-A1 NUCLEOSIDE SUPPLEMENTATION TO PROMOTE CELLULAR FUNCTION, GENETIC STABILITY AND REGENERATIVE APPLICATIONS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2015-04-23 WO disclosed
US-20150105343-A1 NUCLEOSIDE SUPPLEMENTATION TO PROMOTE CELLULAR FUNCTION, GENETIC STABILITY AND REGENERATIVE APPLICATIONS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2015-04-16 US disclosed