Doxribtimine

Doxribtimine

SCHEMBL787593

Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O.O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

P

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SLC28A1 O00337 1/20 0.65
SLC28A2 O43868 1/20 0.65
SLC29A1 Q99808 1/20 0.65
SLC28A3 Q9HAS3 1/20 0.65
TK1 P04183 3/20 0.55
LMNA P02545 2/20 0.55
SMN1; SMN2 Q16637 2/20 0.55
TK2 O00142 1/20 0.54
ALOX12 P18054 1/20 0.52
ADRA1A P35348 1/20 0.52

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 SCHEMBL27538938 0.93 SLC28A1 (0.56) SLC28A1SLC28A2SLC29A1SLC28A3TK1
Doxribtimine SCHEMBL860032 0.91 TK1 (0.62) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL325199 0.91 TK1 (0.62) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL29124320 0.91 P2RY2 (0.60) SLC28A1SLC28A2SLC29A1SLC28A3TK1
Doxribtimine SCHEMBL28320997 0.90 TK1 (0.61) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL27210303 0.90 SLC28A1 (0.51) SLC28A1SLC28A2SLC29A1SLC28A3TK1
Uridine SCHEMBL28025505 0.89 SLC28A1 (0.78) SLC28A1SLC28A2SLC29A1SLC28A3TK2
Uridine SCHEMBL9075559 0.89 SLC28A1 (0.78) SLC28A1SLC28A2SLC29A1SLC28A3TK2
Uridine SCHEMBL2563446 0.89 SLC28A1 (0.78) SLC28A1SLC28A2SLC29A1SLC28A3TK1
Idoxuridine SCHEMBL10383338 0.89 TK1 (0.72) SLC28A1SLC28A2SLC29A1SLC28A3TK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190003966-A1 Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy SENA RESEARCH, INCORPORATED (US) 2019-01-03 US claimed
US-20130183765-A1 Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy Sena Research Incorporated (US) 2013-07-18 US claimed
WO-2012037158-A2 ULTRAVIOLET AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHODS FOR THE EVALUATION OF SUNSCREEN EFFICACY SENA RESEARCH, INCORPORATED (US) 2012-03-22 WO claimed
CN-117016549-B Application of nucleoside compound and composition thereof in promoting plant growth 山东蓬勃生物科技有限公司 2024-02-27 CN disclosed
US-20230405003-A1 APPLICATION OF THYMIDINE DERIVATIVE IN PREPARATION OF DRUGS ONQUALITY PHARMACEUTICALS CHINA LTD. (CN) 2023-12-21 US disclosed
CN-117016549-A Application of nucleoside compound and composition thereof in promoting plant growth 山东蓬勃生物科技有限公司 2023-11-10 CN disclosed
EP-4238571-A1 APPLICATION OF THYMIDINE DERIVATIVE IN PREPARATION OF DRUGS OnQuality Pharmaceuticals China Ltd. (CN) 2023-09-06 EP disclosed
CN-116367842-A Application of thymidine derivative in preparing medicine 上海岸阔医药科技有限公司 2023-06-30 CN disclosed
US-20190003966-A1 Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy SENA RESEARCH, INCORPORATED (US) 2019-01-03 US disclosed
US-10073033-B2 Ultraviolet and high-performance liquid chromatography methods for the evaluation of sunscreen efficacy SENA RESEARCH, INC. (US) 2018-09-11 US disclosed
US-20180119217-A1 MODIFIED NUCLEOTIDES AND USES THEREOF Life Technologies Corporation (US) 2018-05-03 US disclosed
WO-2016153999-A1 MODIFIED NUCLEOTIDES AND USES THEREOF Life Technologies Corporation (US) 2016-09-29 WO disclosed
CN-103232511-B Light-cleavable group protected deoxyuridine triphosphate derivatives and a synthesis method and applications thereof. UNIV BEIJING 2015-06-17 CN disclosed
CN-103232511-A Light-cleavable group protected deoxyuridine triphosphate derivatives and a synthesis method and applications thereof. UNIV BEIJING 2013-08-07 CN disclosed
US-20130183765-A1 Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy Sena Research Incorporated (US) 2013-07-18 US disclosed
WO-2012037158-A2 ULTRAVIOLET AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHODS FOR THE EVALUATION OF SUNSCREEN EFFICACY SENA RESEARCH, INCORPORATED (US) 2012-03-22 WO disclosed
CN-100546589-C The preparation of caterpillar fungus cephalosporin powder anti-arrhythmia effective part and pharmaceutical preparation thereof ZHEJIANG MODERN CHINESE MEDICI (CN) 2009-10-07 CN disclosed
CN-1899319-A Preparation of caterpillar fungus cephalosporin powder anti-arrhythmia effective part and its medicinal preparation ZHEJIANG MODERN CHINESE MEDICI (CN) 2007-01-24 CN disclosed
CN-1603248-A Biological denitrification method for ammonium-nitrogen containing waste water and microbes thereof INST OF SOIL SCIENCE CHINESE A (CN) 2005-04-06 CN disclosed
CN-1076356-C protein having thrombopoietin activity KIRIN BREWERY (JP) 2001-12-19 CN 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-20230405003-A1 APPLICATION OF THYMIDINE DERIVATIVE IN PREPARATION OF DRUGS TYMP, DCTD, TYMS SLC28A1 52/4885SLC28A2 50/4885SLC29A1 22/4885

“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.