Uridine

Uridine

SCHEMBL329746

O=c1ccn([C@@H]2O[C@@H](CO)[C@H](O)[C@@H]2O)c(=O)[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ SLC28A1 O00337 1/20 1.00
▸ SLC28A2 O43868 1/20 1.00
▸ SLC29A1 Q99808 1/20 1.00
▸ SLC28A3 Q9HAS3 1/20 1.00
▸ P2RY2 P41231 11/20 0.69
▸ P2RY6 Q15077 8/20 0.65
▸ P2RY4 P51582 4/20 0.63
▸ P2RY14 Q15391 7/20 0.63

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
Uridine SCHEMBL14853938 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL2056533 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL10815678 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL2056827 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL9060684 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL375985 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Arauridine SCHEMBL359587 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL7752140 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL20987631 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL1804774 1.00 SLC28A1 (1.00) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2

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 88 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0788506-A2 L-RIBOFURANOSYL NUCLEOSIDES GENENCOR INTERNATIONAL, INC. (US) 1997-08-13 — — EP claimed
US-5559101-A ANTITUMOR, ANTICARCINOGENIC, HIV GENENCOR INTERNATIONAL, INC. (US) 1996-09-24 — — US claimed
US-10882903-B2 Methods and compositions for treating an alphavirus infection ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2021-01-05 — — US disclosed
US-10869873-B2 Methods and compositions for treating viral diseases THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2020-12-22 — — US disclosed
EP-2787999-B1 METHODS AND COMPOSITIONS FOR TREATING VIRAL DISEASES UNIV LELAND STANFORD JUNIOR (US) 2019-01-23 — — EP disclosed
US-20180134778-A1 METHODS AND COMPOSITIONS FOR TREATING AN ALPHAVIRUS INFECTION ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2018-05-17 — — US disclosed
US-20180000926-A1 METHODS OF INDUCING AN IMMUNE RESPONSE TO HEPATITIS C VIRUS AGRAWAL, BABITA (CA) 2018-01-04 — — US disclosed
US-20170000802-A1 Methods and Compositions for Treating Viral Diseases THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2017-01-05 — — US disclosed
CN-103145715-B Huge ring carboxylic acid and acyl sulfonamides as HCV replication inhibitors F·霍夫曼-罗须公司 2016-08-03 — — CN disclosed
US-9364484-B2 Methods and compositions for treating viral diseases THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2016-06-14 — — US disclosed
EP-3025727-A1 METHODS OF TREATING LIVER DISEASE The J. David Gladstone Institutes (US) 2016-06-01 — — EP disclosed
CN-1889970-A Macrocyclic carboxylic acids and acylsulfonamides as inhibitors of HCV replication INTERMUNE INC (US) 2007-01-03 — — CN disclosed
US-20060269517-A1 Use of alpha-glucosidase inhibitors to treat alphavirus infections INTERMUNE, INC. 2006-11-30 — — US disclosed
US-20060204473-A1 Synthetic hyperglycosylated, and hyperglycosylated protease-resistant polypeptide variants, oral formulations and methods of using the same ALIOS BIOPHARMA, INC. 2006-09-14 — — US disclosed
US-20060182716-A1 Synthetic hyperglycosylated, protease-resistant polypeptide variants, oral formulations and methods of using the same ALIOS BIOPHARMA, INC. 2006-08-17 — — US disclosed
US-20050267018-A1 Macrocyclic compounds as inhibitors of viral replication HOFFMANN-LA ROCHE INC. 2005-12-01 — — US disclosed
WO-2005095403-A2 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION INTERMUNE, INC. (US) 2005-10-13 — — WO disclosed
WO-2003039523-A2 OLIGONUCLEOTIDES MODIFIED WITH NOVEL α-L-RNA ANALOGUES EXIQON A/S (DK) 2003-05-15 — — WO disclosed
EP-0788506-A2 L-RIBOFURANOSYL NUCLEOSIDES GENENCOR INTERNATIONAL, INC. (US) 1997-08-13 — — EP disclosed
US-5559101-A ANTITUMOR, ANTICARCINOGENIC, HIV GENENCOR INTERNATIONAL, INC. (US) 1996-09-24 — — 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 (5 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-20060182716-A1 Synthetic hyperglycosylated, protease-resistant polypeptide variants, oral formulations and methods of using the same IFNAR1, IDE, CTSC SLC28A1 2154/4885SLC28A2 2642/4885SLC29A1 2625/4885
US-20060269517-A1 Use of alpha-glucosidase inhibitors to treat alphavirus infections GBA3, GAA, GANAB SLC28A1 697/4885SLC28A2 964/4885SLC29A1 1794/4885
US-20050267018-A1 Macrocyclic compounds as inhibitors of viral replication EIF2AK2, HAVCR2, ZC3HAV1 SLC28A1 2104/4885SLC28A2 2897/4885SLC29A1 1180/4885
US-20060204473-A1 Synthetic hyperglycosylated, and hyperglycosylated protease-resistant polypeptide variants, oral formulations and methods of using the same IFNAR1, EPOR, HBB SLC28A1 1018/4885SLC28A2 1518/4885SLC29A1 629/4885
US-20180000926-A1 METHODS OF INDUCING AN IMMUNE RESPONSE TO HEPATITIS C VIRUS HAVCR2, CD74, IFNG SLC28A1 2560/4885SLC28A2 2476/4885SLC29A1 4047/4885

“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.

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