Troxacitabine

Troxacitabine

SCHEMBL1844439

Nc1ccn([C@H]2CO[C@@H](CO)O2)c(=O)n1

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

POLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PRIM1PRIM2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLA1 known ✓ P09884 1/20 0.37
LMNA P02545 3/20 0.60
PDE3A Q14432 3/20 0.60
ALB P02768 3/20 0.60
CACNA1F O60840 2/20 0.60
MAPT P10636 2/20 0.60
CACNA1D Q01668 2/20 0.60
CACNA1S Q13698 2/20 0.60
CACNA1C Q13936 2/20 0.60
THRB P10828 1/20 0.53
MTOR P42345 1/20 0.53
MDM2 Q00987 1/20 0.53
NCOA1 Q15788 1/20 0.53
NCOA3 Q9Y6Q9 1/20 0.53
PDE4D Q08499 1/20 0.50
SLC29A1 Q99808 1/20 0.50
POLG P54098 2/20 0.43
POLB P06746 1/20 0.43
FGFR1 P11362 1/20 0.41
NT5E P21589 1/20 0.39

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
Troxacitabine SCHEMBL1026150 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL18548 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL1026148 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL1653267 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL6424800 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL30317744 1.00 LMNA (0.60) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL22285889 0.99 LMNA (0.59) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL17542009 0.95 LMNA (0.56) LMNAPDE3AALBCACNA1FMAPT
Troxacitabine SCHEMBL7560355 0.89 POLG (0.59) LMNAPDE3AALBCACNA1FMAPT
SCHEMBL31347648 0.88 LMNA (0.59) LMNAPDE3AALBCACNA1FMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070259832-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2007-11-08 US claimed
EP-1485395-A2 NUCLEOTIDE MIMICS AND THEIR PRODRUGS Biota, Inc. (US) 2004-12-15 EP claimed
WO-2003072757-A9 NUCLEOTIDE MIMICS AND THEIR PRODRUGS BIOTA INC (US) 2004-10-21 WO claimed
US-20040059104-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2004-03-25 US claimed
WO-2003072757-A2 NUCLEOTIDE MIMICS AND THEIR PRODRUGS BIOTA, INC. (US) 2003-09-04 WO claimed
WO-2025072236-A1 PUBLISHING DEVICE PUBLIC INFORMATION IN A WIRELESS BLOCKCHAIN SYSTEM INTERDIGITAL PATENT HOLDINGS, INC. (US) 2025-04-03 WO disclosed
CN-118295995-B Multi-source geological data standardization processing method and system 江西省地质博物馆 2024-08-13 CN disclosed
CN-118295995-A Multi-source geological data standardization processing method and system 江西省地质博物馆 2024-07-05 CN disclosed
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-01-02 US disclosed
CN-116842032-A Commodity vector retrieval method and system based on contrast learning and commodity entity 北京永辉科技有限公司 2023-10-03 CN disclosed
EP-2322518-B1 Method of manufacture of 1,3-dioxolane and 1,3-oxathiolane nucleosides GILEAD SCIENCES INC (US) 2015-02-25 EP disclosed
EP-2509990-A1 NOVEL PHOSPH(ON)ATE- AND SULF(ON)ATE-BASED PHOSPHATE MODIFIED NUCLEOSIDES USEFUL AS SUBSTRATES FOR POLYMERASES AND AS ANTIVIRAL AGENTS Katholieke Universiteit Leuven, K.U. Leuven R&D (BE) 2012-10-17 EP disclosed
US-20030144532-A1 Method of manufacture of 1,3-oxathiolane nucleosides GILEAD SCIENCES, INC. 2003-07-31 US disclosed
US-6576776-B1 Method of manufacture of 1,3-oxathiolane nucleosides TRIANGLE PHARMACEUTICALS, INC. 2003-06-10 US disclosed
US-6566365-B1 Administering a therapeutically effective amount of nucleoside analog compound for therapy of Flaviviridea viral infection in a host BIOCHEM PHARMA INC. (CA) 2003-05-20 US disclosed
US-6518425-B1 A process for producing a 1,3-oxathiolane nucleoside comprising reacting a 5-halo-2-protected-oxymethyl-1,3-oxathiolane with a silylated purine or pyrimidine without the addition of a Lewis acid or an additional base to the reaction EMORY UNIVERSITY 2003-02-11 US disclosed
US-6350753-B1 2-ACETOXYMETHYL-4-(THYMIN-1'-YL)-1,3,-DIOXOLANE; 2-BENZOYLOXYMETHYL-4-(CYTOSIN-1'-YL)-1,3-DIOXOLANE; ANTIVIRAL AGENTS, PARTICULARY FOR THE TREATMENT OF THE HIV INFECTIONS IN MAMMALS, ESPECIALLY HUMANS BIOCHEM PHARMA INC. (CA) 2002-02-26 US disclosed
EP-1104415-A1 METHOD OF MANUFACTURE OF 1,3-OXATHIOLANE NUCLEOSIDES Triangle Pharmaceuticals Inc. (US) 2001-06-06 EP disclosed
US-6215004-B1 CYCLIZATION OF MERCAPTOACETIC ACID WITH ACETAL IN SOLVENT; SULFIDING EMORY UNIVERSITY 2001-04-10 US disclosed
WO-2000009494-A1 METHOD OF MANUFACTURE OF 1,3-OXATHIOLANE NUCLEOSIDES TRIANGLE PHARMACEUTICALS, INC. (US) 2000-02-24 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 (4 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-20070259832-A1 Nucleotide mimics and their prodrugs NUDT14, ENTPD5, MTAP POLA1 909/4885LMNA 3677/4885PDE3A 765/4885
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules PIK3CA, CHAMP1, TYMP POLA1 198/4885LMNA 1794/4885PDE3A 2076/4885
US-20030144532-A1 Method of manufacture of 1,3-oxathiolane nucleosides NUDT1, PNP, TYMP POLA1 116/4885LMNA 989/4885PDE3A 637/4885
US-20040059104-A1 Nucleotide mimics and their prodrugs NUDT14, ENTPD5, MTAP POLA1 909/4885LMNA 3677/4885PDE3A 765/4885

“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.