Doxribtimine

Doxribtimine

SCHEMBL2985309

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

nearest known ligand 0.69

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 7)

geneUniProtsupporting neighboursconfidence
TK1 P04183 3/20 0.65
LMNA P02545 2/20 0.65
SMN1; SMN2 Q16637 2/20 0.65
TK2 O00142 1/20 0.63
ALOX12 P18054 1/20 0.61
ADRA1A P35348 1/20 0.61
RNASE1 P07998 1/20 0.60

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 SCHEMBL20214217 0.94 TK1 (0.69) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL8023808 0.94 TK1 (0.72) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL993448 0.93 TK1 (0.67) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL14596596 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL767986 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL2722555 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL10382149 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL12296879 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL21078835 0.93 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL13497202 0.93 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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7777023-B2 Method for the chemical synthesis of oligonucleotides SIRNA THERAPEUTICS, INC. (US) 2010-08-17 US claimed
US-6995259-B1 Method for the chemical synthesis of oligonucleotides SIRNA THERAPEUTICS, INC. (US) 2006-02-07 US claimed
EP-1401852-B1 METHODS FOR PREPARING OLIGONUCLEOTIDES HAVING CHIRAL PHOSPHOROTHIOATE LINKAGES ISIS PHARMACEUTICALS INC (US) 2013-09-11 EP disclosed
EP-1401852-A4 METHODS FOR PREPARING OLIGONUCLEOTIDES HAVING CHIRAL PHOSPHOROTHIOATE LINKAGES ISIS PHARMACEUTICALS INC (US) 2006-08-09 EP disclosed
US-20060041115-A1 Methods for preparing oligonucleotides having chiral phosphorothioate linkages ISIS PHARMACEUTICALS, INC. 2006-02-23 US disclosed
EP-1401852-A2 METHODS FOR PREPARING OLIGONUCLEOTIDES HAVING CHIRAL PHOSPHOROTHIOATE LINKAGES ISIS Pharmaceuticals, Inc. (US) 2004-03-31 EP disclosed
US-20030069410-A1 Methods for preparing oligonucleotides having chiral phosphorothioate linkages ISIS PHARMACEUTICALS, INC. 2003-04-10 US disclosed
WO-2002102815-A2 METHODS FOR PREPARING OLIGONUCLEOTIDES HAVING CHIRAL PHOSPHOROTHIOATE LINKAGES ISIS PHARMACEUTICALS, INC. (US) 2002-12-27 WO disclosed
WO-1994001446-A2 DERIVATIZED ORGANIC SOLID SUPPORT FOR NUCLEIC ACID SYNTHESIS BECKMAN INSTRUMENTS, INC. (US) 1994-01-20 WO disclosed
US-4812512-A SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES ROUSSEL UCLAF (FR) 1989-03-14 US disclosed
US-4780504-A POLYLACTAMS LINKED TO SILICA MICROPELLETS ROUSSEL UCLAF (FR) 1988-10-25 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 (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-20060041115-A1 Methods for preparing oligonucleotides having chiral phosphorothioate linkages RNGTT, NUDT1, NSUN2 TK1 151/4885LMNA 612/4885SMN1; SMN2 863/4885
US-20030069410-A1 Methods for preparing oligonucleotides having chiral phosphorothioate linkages RNGTT, TYMP, POLN TK1 97/4885LMNA 650/4885SMN1; SMN2 315/4885

“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.