Uridine

Uridine

SCHEMBL376208

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

nearest known ligand 0.90

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
SLC28A1 O00337 1/20 0.90
SLC28A2 O43868 1/20 0.90
SLC29A1 Q99808 1/20 0.90
SLC28A3 Q9HAS3 1/20 0.90
P2RY2 P41231 11/20 0.74
P2RY6 Q15077 8/20 0.69
P2RY4 P51582 4/20 0.68
P2RY14 Q15391 7/20 0.67

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 SCHEMBL157643 1.00 SLC28A1 (0.90) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL30094506 1.00 SLC28A1 (0.90) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL29801499 1.00 SLC28A1 (0.90) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL28065954 1.00 SLC28A1 (0.90) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL76681 1.00 SLC28A1 (0.90) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL28131489 0.99 SLC28A1 (0.88) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL17074124 0.99 SLC28A1 (0.88) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL2370972 0.99 SLC28A1 (0.88) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL17439380 0.95 SLC28A1 (0.85) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
Uridine SCHEMBL5330850 0.95 SLC28A1 (0.85) 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 48 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111662350-B Preparation method of green intelligent high-purity diquafosol tetrasodium 南京宸翔医药研究有限责任公司 2022-06-07 CN disclosed
WO-2021117837-A1 IONIC-GROUP-CONTAINING MICROBALLOON AND PRODUCTION METHOD THEREFOR 株式会社トクヤマ 2021-06-17 WO disclosed
CN-111662350-A Preparation method of green intelligent high-purity diquafosol tetrasodium 南京宸翔医药研究有限责任公司 2020-09-15 CN disclosed
CN-110981928-A Method for producing uridylic acid disodium by continuous flow reaction device 美亚药业海安有限公司 2020-04-10 CN disclosed
CN-110885812-A Method for preparing uridylic acid by enzyme method 杭州唯泰生物药业有限公司 2020-03-17 CN disclosed
EP-1644394-B1 SYNTHESIS AND COMPOSITIONS OF 2 -TERMINATOR NUCLEOTIDES ROCHE DIAGNOSTICS GMBH (DE) 2018-05-09 EP disclosed
EP-1641943-B1 2'-TERMINATOR NUCLEOTIDE-RELATED METHODS AND SYSTEMS ROCHE DIAGNOSTICS GMBH (DE) 2013-03-20 EP disclosed
US-8163487-B2 2′-terminator nucleotide-related methods and systems ROCHE MOLECULAR SYSTEMS, INC. (US) 2012-04-24 US disclosed
EP-2076606-B1 2'-TERMINATOR RELATED PYROPHOSPHOROLYSIS ACTIVATED POLYMERIZATION ROCHE DIAGNOSTICS GMBH (DE) 2012-01-25 EP disclosed
US-20110201002-A1 2'-Terminator Nucleotide-Related Methods and Systems ROCHE MOLECULAR SYSTEMS, INC. (US) 2011-08-18 US disclosed
US-6765090-B2 DRUGS; STABILITY, SOLUBILITY, NONTOXIC, EASY TO HANDLE INSPIRE PHARMACEUTICALS, INC. 2004-07-20 US disclosed
US-6713458-B1 DRY EYE; RETINAL DETACHMENT INSPIRE PHARMACEUTICALS, INC. 2004-03-30 US disclosed
EP-1012154-B1 SALTS OF DI(URIDINE 5'-TETRAPHOSPHATE), METHOD FOR PREPARATION AND USES THEREOF INSPIRE PHARMACEUTICALS INC (US) 2004-03-17 EP disclosed
US-20040014713-A1 Di(uridine 5')-tetraphosphate and salts thereof MERCK SHARP & DOHME CORP. 2004-01-22 US disclosed
US-6548658-B2 Tetrasodium, ammonium, lithium and potassium salts of P1, P4-di(uridine 5')-tetraphosphate; stable, soluble, nontoxic, of high purity and easy to handle during manufacture INSPIRE PHARMACEUTICALS, INC. 2003-04-15 US disclosed
US-20020086851-A1 Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof MERCK SHARP & DOHME CORP. 2002-07-04 US disclosed
US-6319908-B1 FOR THERAPY CYSTIC FIBROSIS, CHRONIC BRONCHITIS, ASTHMA, BRONCHIECTASIS, POST-OPERATIVE MUCOUS RETENTION, PNEUMONIA, PRIMARY CILIARY DYSKINESIA INSPIRE PHARMACEUTICALS, INC. 2001-11-20 US disclosed
US-20010011079-A1 Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof MERCK SHARP & DOHME CORP. 2001-08-02 US disclosed
EP-1012154-A2 SALTS OF DI(URIDINE 5'-TETRAPHOSPHATE), METHOD FOR PREPARATION AND USES THEREOF Inspire Pharmaceuticals, Inc. (US) 2000-06-28 EP disclosed
WO-1999005155-A2 SALTS OF DI(URIDINE 5'-TETRAPHOSPHATE), METHOD FOR PREPARATION AND USES THEREOF INSPIRE PHARMACEUTICALS, INC. (US) 1999-02-04 WO 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-20020086851-A1 Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof UMPS, NUDT1, ITPA SLC28A1 45/4885SLC28A2 53/4885SLC29A1 34/4885
US-20040014713-A1 Di(uridine 5')-tetraphosphate and salts thereof UMPS, NUDT1, UPP1 SLC28A1 63/4885SLC28A2 110/4885SLC29A1 26/4885
US-20010011079-A1 Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof UMPS, NUDT1, UPP1 SLC28A1 65/4885SLC28A2 111/4885SLC29A1 25/4885

“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.