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cladribine

Structure via PubChem · Public domain (PubChem)

EntityQ414030· pop 21· linked from 522 articles

cladribine

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Also known as (2R,3S,5R)-5-(6-amino-2-Chloropurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol, Cladribina, 2-chloro-6-amino-9-(2-Deoxy-beta-D-erythro-pentofuranosyl)purine, Cladribinum, 2-Chlorodeoxyadenosine, 2-CdA, 2-chloro-Deoxyadenosine, 2-Chloro-2'-deoxy-beta-adenosine

Cladribine, sold under the brand name Leustatin, among others, is a medication used to treat hairy cell leukemia (formally named leukemic reticuloendotheliosis) and B-cell chronic lymphocytic leukemia. Cladribine, sold under the brand name Mavenclad, is used for the treatment of adults with highly active forms of relapsing-remitting multiple sclerosis.

Key facts

Drug.Watchedfields
changed
Drug.verifiedrevid
460040776
Drug.IUPAC_name
5-(6-Amino-2-chloro-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol
Drug.image
Cladribine.svg
Drug.image_class
skin-invert-image
Drug.width
200
Drug.tradename
Leustatin, Litak, Mavenclad, others
Drug.synonyms
2-Chlorodeoxyadenosine; 2-Chloro-2'-deoxyadenosine; 2-CdA
Drug.MedlinePlus
a693015
Drug.DailyMedID
Cladribine
Drug.pregnancy_AU
D
Drug.routes_of_administration
Intravenous, subcutaneous (liquid), by mouth (tablet)
Drug.ATC_prefix
L01
Drug.ATC_suffix
BB04
Drug.ATC_supplemental
(parenteral) (oral for multiple sclerosis)
Drug.legal_AU
S4
Drug.legal_CA
Rx-only
Drug.legal_UK
POM

via Wikipedia infobox

Chemical data

Formula
C10H12ClN5O3
Molecular weight
285.69 g/mol
IUPAC name
(2R,3S,5R)-5-(6-amino-2-chloropurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol
SMILES
C1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=C(N=C32)Cl)N)CO)O
InChIKey
PTOAARAWEBMLNO-KVQBGUIXSA-N
XLogP
0.8
Polar surface area
119 Ų
H-bond donors
3
H-bond acceptors
7
Formal charge
0

via PubChem

Research

2,934 papers

via PubMed

Wikidata facts

Mass
285.062867
Show 6 more facts
chemical formula
C₁₀H₁₂ClN₅O₃
NCI Thesaurus ID
C1336
isomeric SMILES
NC1=NC(Cl)=NC2=C1N=CN2[C@H]3C[C@H](O)[C@@H](CO)O3
canonical SMILES
C1C(C(OC1N2C=NC3=C2N=C(N=C3N)Cl)CO)O
Commons category
Cladribine
defined daily dose
0.34
Sources (10)

via Wikidata · CC0

~16 min read

Article

11 sections
Contents
  • Medical uses
  • Multiple sclerosis
  • Side effects
  • In hairy cell leukemia
  • In multiple sclerosis
  • Mechanism of action
  • History
  • Hairy cell leukemia
  • Multiple sclerosis
  • Research
  • References

Cladribine, sold under the brand name Leustatin, among others, is a medication used to treat hairy cell leukemia (formally named leukemic reticuloendotheliosis) and B-cell chronic lymphocytic leukemia. Cladribine, sold under the brand name Mavenclad, is used for the treatment of adults with highly active forms of relapsing-remitting multiple sclerosis.

Cladribine is a purine analogue that selectively targets and suppresses lymphocytes implicated in the underlying pathogenesis of multiple sclerosis and B-cell leukaemia. Chemically, it mimics the nucleoside deoxyadenosine. However, unlike deoxyadenosine, it is relatively resistant to breakdown by the enzyme adenosine deaminase, which causes it to accumulate in targeted cells and interfere with the cell's ability to process DNA. Cladribine is taken up by cells via transporter proteins. Once inside a cell, cladribine undergoes phosphorylation by the enzyme deoxycytidine kinase (DCK) to produce mononucleotide 2-chlorodeoxyadenosine 5'monophosphate (2-CdAMP), which is subsequently phosphorylated to the triphosphorylated active compound 2-chlorodeoxyadenosine 5'triphosphate (2-CdATP). Activated cladribine is incorporated into cellular DNA, which triggers apoptosis. Accumulation of cladribine into cells is dependent on the ratio of DCK and 5'-nucleotidase (5'-NT), which breaks down and inactivates the compound. This ratio differs between cell types, with high levels in T and B lymphocytes, resulting in selective targeting of these cells. In contrast, DCK:5'NT is relatively low in other cell types, thus sparing numerous non-haematological cells.

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