Zalcitabine

Zalcitabine

SCHEMBL285163

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

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

The experimentally established mechanism targets of Zalcitabine. 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
ABL1 P00519 1/20 0.57
RIN1 Q13671 1/20 0.57
LMNA P02545 4/20 0.57
PDE3A Q14432 3/20 0.57
ALB P02768 3/20 0.57
CACNA1F O60840 2/20 0.57
MAPT P10636 2/20 0.57
CACNA1D Q01668 2/20 0.57
CACNA1S Q13698 2/20 0.57
CACNA1C Q13936 2/20 0.57
POLG P54098 2/20 0.53
THRB P10828 1/20 0.50
MTOR P42345 1/20 0.50
MDM2 Q00987 1/20 0.50
NCOA1 Q15788 1/20 0.50
NCOA3 Q9Y6Q9 1/20 0.50
POLB P06746 1/20 0.48
PDE4D Q08499 1/20 0.47
SLC29A1 Q99808 1/20 0.47
ALDH1A1 P00352 1/20 0.44

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
Zalcitabine SCHEMBL211115 1.00 ABL1 (0.57) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL6913582 0.95 ABL1 (0.55) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL12149465 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL598496 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL3715526 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL21100417 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL3235525 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL3598 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL8094882 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB
Zalcitabine SCHEMBL9194365 0.95 LMNA (0.62) ABL1RIN1LMNAPDE3AALB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014031954-A1 HOMOPOLYMER MEDIATED NUCLEIC ACID AMPLIFICATION TUFTS UNIVERSITY (US) 2014-02-27 WO claimed
EP-2428201-A1 Oral administration of nucleoside monophosphates Merck Serono S.A. (CH) 2012-03-14 EP claimed
US-6498036-B1 Methods of targeting a chromosomal gene sequence in a eukaryotic cell TRUSTEES OF AMHERST COLLEGE 2002-12-24 US claimed
EP-2614156-B1 CONTROL OF DNA MOVEMENT IN A NANOPORE AT ONE NUCLEOTIDE PRECISION BY A PROCESSIVE ENZYME UNIV CALIFORNIA (US) 2018-08-01 EP disclosed
US-9914950-B2 Homopolymer mediated nucleic acid amplification TUFTS UNIVERSITY (US) 2018-03-13 US disclosed
US-20150203887-A1 HOMOPOLYMER MEDIATED NUCLEIC ACID AMPLIFICATION TUFTS UNIVERSITY (US) 2015-07-23 US disclosed
WO-2014031954-A1 HOMOPOLYMER MEDIATED NUCLEIC ACID AMPLIFICATION TUFTS UNIVERSITY (US) 2014-02-27 WO disclosed
EP-2614156-A2 CONTROL OF DNA MOVEMENT IN A NANOPORE AT ONE NUCLEOTIDE PRECISION BY A PROCESSIVE ENZYME The Regents of the University of California (US) 2013-07-17 EP disclosed
WO-2012033524-A2 CONTROL OF DNA MOVEMENT IN A NANOPORE AT ONE NUCLEOTIDE PRECISION BY A PROCESSIVE ENZYME THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-03-15 WO disclosed
EP-2428201-A1 Oral administration of nucleoside monophosphates Merck Serono S.A. (CH) 2012-03-14 EP disclosed
EP-1240355-B1 REMOVAL OF DYE-LABELED DIDEOXY TERMINATORS FROM DNA SEQUENCING REACTIONS CAMBREX BIO SCIENCE ROCKLAND I (US) 2008-08-27 EP disclosed
WO-1995029702-A1 TEXAPHYRIN SOLID-SUPPORTS AND DEVICES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1995-11-09 WO disclosed
WO-1994009003-A1 SAPPHYRIN DERIVATIVES, CONJUGATES AND POLYMERS THEREOF AND EXPANDED PORPHYRIN CHROMATOGRAPHIC SUPPORTS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1994-04-28 WO disclosed
US-5223263-A Viricide complex; aids therapy VICAL, INC. (US) 1993-06-29 US disclosed
WO-1992022306-A1 TRANSFORMED ERYTHROCYTES, PROCESS FOR PREPARING THE SAME, AND THEIR USE IN PHARMACEUTICAL COMPOSITIONS COMMUNAUTE ECONOMIQUE EUROPEENNE (CEE) (LU) 1992-12-23 WO disclosed
EP-0517986-A1 Transformed erythrocytes, process for preparing the same, and their use in pharmaceutical compositions COMMUNAUTE ECONOMIQUE EUROPEENNE (CEE) (LU) 1992-12-16 EP disclosed
WO-1990000555-A1 LIPID DERIVATIVES OF ANTIVIRAL NUCLEOSIDES, LIPOSOMAL INCORPORATION AND METHOD OF USE VICAL, INC. (US) 1990-01-25 WO disclosed
EP-0350287-A2 Lipid derivatives of antiviral nucleosides, liposomal incorporation and method of use NeXstar Pharmaceuticals, Inc. (US) 1990-01-10 EP disclosed
WO-1988007854-A1 NEW ANTI-RETROVIRAL AGENTS AND DELIVERY SYSTEM UNITED STATES OF AMERICA, REPRESENTED BY THE UNITE (US) 1988-10-20 WO disclosed
EP-0286418-A1 Anti-retroviral agents and delivery systems for the same THE UNITED STATES OF AMERICA as represented by the Secretary United States Department of Commerce (US) 1988-10-12 EP disclosed