Doxribtimine

Doxribtimine

SCHEMBL860032

Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O.O=c1ccn([C@H]2C[C@H](O)[C@@H](CO)O2)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
TK1 P04183 4/20 0.62
LMNA P02545 3/20 0.62
SMN1; SMN2 Q16637 2/20 0.62
TK2 O00142 1/20 0.61
ALOX12 P18054 1/20 0.59
ADRA1A P35348 1/20 0.59
ALB P02768 1/20 0.58
PKM P14618 1/20 0.58
BLM P54132 1/20 0.58
PMP22 Q01453 1/20 0.58

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 SCHEMBL787593 0.91 SLC28A1 (0.65) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL12718344 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL2722555 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL13497202 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL767986 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL10382149 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL14596596 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL12296879 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL21078835 0.91 TK1 (0.73) TK1LMNASMN1; SMN2TK2ALOX12
Doxribtimine SCHEMBL3437224 0.91 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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113755416-B Recombinant microorganism having novel synthetic pathway for producing beta-thymidine and method for producing beta-thymidine 苏州华赛生物工程技术有限公司 2023-08-15 CN disclosed
CN-113755416-A Recombinant microorganism with novel synthetic pathway for producing beta-thymidine and method for producing beta-thymidine 苏州华赛生物工程技术有限公司 2021-12-07 CN disclosed
CN-101838696-B For the pearl of high-throughput nucleic acid analysis F. HOFFMANN-LA ROCHE AG (CH) 2015-11-25 CN disclosed
CN-101845494-B Miniaturized, high-throughput nucleic acid analysis F. HOFFMANN-LA ROCHE AG (CH) 2015-11-25 CN disclosed
CN-101418340-B Diagnostic test for susceptibility to b-raf kinase inhibitors HOFFMANN LA ROCHE 2014-05-07 CN disclosed
EP-2434421-A2 Compositions and methods for modeling saccharomyces cerevisiae metabolism The Regents of The University of California (US) 2012-03-28 EP disclosed
CN-101845494-A Miniaturized, high-throughput nucleic acid analysis HOFFMANN LA ROCHE 2010-09-29 CN disclosed
CN-101838696-A The pearl that is used for high-throughput nucleic acid analysis HOFFMANN LA ROCHE 2010-09-22 CN disclosed
CN-101418340-A The diagnostic detection of B-RAF kinase inhibitor susceptibility HOFFMANN LA ROCHE (CH) 2009-04-29 CN disclosed
CN-100385009-C Method of preparing a guanosine-group compound and an intermediate thereof YUKI GOSEI YAKUHIN KOGYO KK (JP) 2008-04-30 CN disclosed
CN-100350052-C Method of preparing a guanosine-group compound and an intermediate thereof YUKI GOSEI YAKUHIN KOGYO KK (JP) 2007-11-21 CN disclosed
CN-1821420-A Method of preparing a guanosine-group compound and an intermediate thereof YUKI GOSEI YAKUHIN KOGYO KK (JP) 2006-08-23 CN disclosed
CN-1818074-A Method of preparing a guanosine-group compound and an intermediate thereof YUKI GOSEI YAKUHIN KOGYO KK (JP) 2006-08-16 CN disclosed
CN-1818073-A Method of preparing a guanosine-group compound and an intermediate thereof YUKI GOSEI YAKUHIN KOGYO KK (JP) 2006-08-16 CN disclosed
CN-1243833-C Process for preparing guanosine-group compounds and intermediates thereof ORGANIC SYNTHETIC PHARMACEUTIC (JP) 2006-03-01 CN disclosed
CN-1320706-A Process for preparing guanosine-group compounds and intermediates thereof ORGANIC SYNTHETIC PHARMACEUTIC (JP) 2001-11-07 CN disclosed