Doxribtimine

Doxribtimine

SCHEMBL542736

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

nearest known ligand 0.77

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 11)

geneUniProtsupporting neighboursconfidence
▸ TK1 P04183 4/20 0.73
▸ LMNA P02545 3/20 0.73
▸ SMN1; SMN2 Q16637 2/20 0.73
▸ TK2 O00142 1/20 0.71
▸ ALOX12 P18054 1/20 0.69
▸ ADRA1A P35348 1/20 0.69
▸ ALB P02768 1/20 0.67
▸ PKM P14618 1/20 0.67
▸ BLM P54132 1/20 0.67
▸ PMP22 Q01453 1/20 0.67
▸ TSHR P16473 1/20 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
Doxribtimine SCHEMBL778861 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL4201980 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL16189745 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL12286396 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL2922181 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL7882259 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL3437225 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL23486 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL21078835 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL3437224 1.00 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115181147-B Preparation method of C4 '-trifluoromethylthio modified nucleoside and C4' -trifluoromethylthio modified nucleic acid 南开大学 2024-04-02 — — CN claimed
CN-115181147-A Preparation method of C4 '-trifluoromethylthio modified nucleoside and C4' -trifluoromethylthio modified nucleic acid 南开大学 2022-10-14 — — CN claimed
US-8110676-B2 Prodrugs activated by RNA-dependent DNA-polymerases PROTERA S.R.L. (IT) 2012-02-07 — — US claimed
EP-4688781-A1 METHODS AND REAGENTS FOR SYNTHESIZING HALOALDEHYDES, AND USES THEREOF Simon Fraser University (CA) 2026-02-11 — — EP disclosed
WO-2024201390-A1 METHODS AND REAGENTS FOR SYNTHESIZING HALOALDEHYDES, AND USES THEREOF SIMON FRASER UNIVERSITY (CA) 2024-10-03 — — WO disclosed
WO-2024201393-A1 METHODS FOR THE SYNTHESIS OF NUCLEOSIDE ANALOGUES AND NUCLEOSIDES ANALOGUES DERIVED THEREFROM SIMON FRASER UNIVERSITY (CA) 2024-10-03 — — WO disclosed
CN-115181147-B Preparation method of C4 '-trifluoromethylthio modified nucleoside and C4' -trifluoromethylthio modified nucleic acid 南开大学 2024-04-02 — — CN disclosed
US-20230159922-A1 MODIFIED OLIGOMERIC COMPOUNDS AND USES THEREOF IONIS PHARMACEUTICALS, INC. (US) 2023-05-25 — — US disclosed
US-20230159922-A1 MODIFIED OLIGOMERIC COMPOUNDS AND USES THEREOF IONIS PHARMACEUTICALS, INC. (US) 2023-05-25 — — US disclosed
US-20230129710-A1 Methods and Reagents for Synthesizing Nucleosides and Analogues Thereof SIMON FRASER UNIVERSITY (CA) 2023-04-27 — — US disclosed
CN-115667280-A Method and reagent for synthesizing nucleoside and analogue thereof 西蒙弗雷泽大学 2023-01-31 — — CN disclosed
CN-115181147-A Preparation method of C4 '-trifluoromethylthio modified nucleoside and C4' -trifluoromethylthio modified nucleic acid 南开大学 2022-10-14 — — CN disclosed
WO-2021030763-A1 MODIFIED OLIGOMERIC COMPOUNDS AND USES THEREOF IONIS PHARMACEUTICALS, INC. (US) 2021-02-18 — — WO disclosed
US-5449664-A Nucleosides SYNTEX (U.S.A.) INC. (US) 1995-09-12 — — US disclosed
US-5192749-A Viricide, AIDS SYNTEX (U.S.A.) INC. (US) 1993-03-09 — — US disclosed
EP-0457326-A1 Antiviral agents SYNTEX (U.S.A.) INC. (US) 1991-11-21 — — EP disclosed
EP-0013625-B1 SOLUBILIZED THYMIDINE COMPOSITION AND METHOD OF PRODUCING SAME Marcus, Israel (IL) 1982-11-17 — — EP disclosed
US-3975374-A Process for preparing 2-thiouracil nucleosides THE UPJOHN COMPANY (US) 1976-08-17 — — 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 (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-20230129710-A1 Methods and Reagents for Synthesizing Nucleosides and Analogues Thereof NUDT1, ADAR, APRT TK1 199/4885LMNA 1420/4885SMN1; SMN2 1952/4885

“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.

Send feedback