Doxribtimine

Doxribtimine

SCHEMBL4958975

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

nearest known ligand 0.68

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 0.65
LMNA P02545 3/20 0.65
SMN1; SMN2 Q16637 1/20 0.65
POLB P06746 1/20 0.64
TK2 O00142 1/20 0.63
TSHR P16473 2/20 0.62
ALB P02768 1/20 0.62
PKM P14618 1/20 0.62
BLM P54132 1/20 0.62
PMP22 Q01453 1/20 0.62
CYP2D6 P10635 1/20 0.62

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 SCHEMBL8217370 1.00 TK1 (0.65) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL8070613 1.00 TK1 (0.65) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL176363 0.95 TK1 (0.67) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL21682515 0.95 TK1 (0.67) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL8075845 0.95 TK1 (0.67) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL77830 0.95 TK1 (0.67) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL887722 0.95 TK1 (0.67) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL9386574 0.94 TK1 (0.66) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL5692278 0.94 TK1 (0.66) TK1LMNASMN1; SMN2POLBTK2
Doxribtimine SCHEMBL7576317 0.94 TK1 (0.66) TK1LMNASMN1; SMN2POLBTK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7223538-B2 Post-synthesis labeling of nucleic acids, assays using nucleic acids that are labeled post-synthetically, single nucleotide polymorphism detection, and associated compounds and microarrays GE HEALTHCARE BIO-SCIENCES AB (SE) 2007-05-29 US claimed
CN-1620515-A Post-synthesis labeling of nucleic acids and uses thereof AMERSHAM BIOSCIENCES AB (SE) 2005-05-25 CN claimed
EP-1461455-A2 POST-SYNTHESIS LABELING OF NUCLEIC ACIDS AND USES THEREOF Amersham Biosciences AB (SE) 2004-09-29 EP claimed
WO-2003052115-A2 POST-SYNTHESIS LABELING OF NUCLEIC ACIDS AND USES THEREOF AMERSHAM BIOSCIENCES AB (SE) 2003-06-26 WO claimed
US-20030119005-A1 Post-synthesis labeling of nucleic acids, assays using nucleic acids that are labeled post-synthetically, single nucleotide polymorphism detection, and associated compounds and microarrays MOTOROLA, INC. 2003-06-26 US claimed
WO-2025068557-A1 ANTISENSE OLIGONUCLEOTIDES FOR THE TREATMENT OF CANAVAN DISEASE CONTERA PHARMA A/S (DK) 2025-04-03 WO disclosed
US-20230340008-A1 BRIDGED NUCLEOSIDE AND NUCLEOTIDE USING SAME JAPAN AS REPRESENTED BY DIRECTOR GENERAL OF NATIONAL INSTITUTE OF HEALTH SCIENCES (JP) 2023-10-26 US disclosed
EP-4108670-A1 BRIDGED NUCLEOSIDE AND NUCLEOTIDE USING SAME OSAKA UNIVERSITY (JP) 2022-12-28 EP disclosed
CN-115151555-A Bridged nucleoside and nucleotide using the same 国立大学法人大阪大学 2022-10-04 CN disclosed
US-20220127300-A1 5'-MODIFIED NUCLEOSIDE AND NUCLEOTIDE USING SAME OSAKA UNIVERSITY (JP) 2022-04-28 US disclosed
EP-3925965-A1 5'-MODIFIED NUCLEOSIDE AND NUCLEOTIDE USING SAME Osaka University (JP) 2021-12-22 EP disclosed
EP-3919501-A1 5'-MODIFIED NUCLEOSIDE AND NUCLEOTIDE USING SAME Osaka University (JP) 2021-12-08 EP disclosed
US-6051699-A Process for the synthesis of oligomeric compounds ISIS PHARMACEUTICALS, INC. (US) 2000-04-18 US disclosed
US-5859232-A Process for the synthesis of oligomeric phosphite, phosphodiester, phosphorothioate and phosphorodithioate compounds ISIS PHARMACEUTICALS, INC. (US) 1999-01-12 US disclosed
EP-0886638-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 1998-12-30 EP disclosed
EP-0870194-A1 CAPILLARY ELECTROPHORETIC SEPARATION METHOD USING A FILLABLE POLYMER SOLUTION AS SEPARATING AGENT Novartis AG (CH) 1998-10-14 EP disclosed
US-5705621-A Oligomeric phosphite, phosphodiester, Phosphorothioate and phosphorodithioate compounds and intermediates for preparing same ISIS PHARMACEUTICALS, INC. (US) 1998-01-06 US disclosed
WO-1997038134-A1 METHOD FOR DETECTING A TARGET COMPOUND USING A NUCLEIC ACID LIGAND NEXSTAR PHARMACEUTICALS, INC. (US) 1997-10-16 WO disclosed
WO-1997024610-A1 CAPILLARY ELECTROPHORETIC SEPARATION METHOD USING A FILLABLE POLYMER SOLUTION AS SEPARATING AGENT NOVARTIS AG (CH) 1997-07-10 WO disclosed
WO-1997019092-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 1997-05-29 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 (2 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-20230340008-A1 BRIDGED NUCLEOSIDE AND NUCLEOTIDE USING SAME SLC29A1, SLC29A2, PNP TK1 53/4885LMNA 1741/4885SMN1; SMN2 699/4885
US-20220127300-A1 5'-MODIFIED NUCLEOSIDE AND NUCLEOTIDE USING SAME NT5C3B, DUT, RNGTT TK1 99/4885LMNA 1449/4885SMN1; SMN2 860/4885

“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.