Dithranol 2% cream
Anthralin (1,8‐dihydroxy‐9anthrone, dithranol) is an older anti-psoriatic agent that was first synthesized as a derivative of chrysarobin, obtained from the araroba tree in Brazil over 100 years ago.
Safety information for pregnancy and breastfeeding
Pregnancy
Always consult your doctor or midwife before taking any medicine during pregnancy or while breastfeeding. Source: DrugBank (CC BY-NC 4.0).
Official documents, adverse reaction reporting, and safety monitoring
Report a side effect
Submit a Yellow Card report to the MHRA
Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
View Drug Analysis Profile
Suspected adverse reactions reported for Dithranol
Browse all iDAP reports
Interactive Drug Analysis Profiles for all medicines
Report a side effect
Submit a Yellow Card report to the MHRA
Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
View EudraVigilance report
Suspected adverse reactions reported for Dithranol
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(4)
Grenz rays therapy for inflammatory skin conditions (HTG151)
Deucravacitinib for treating moderate to severe plaque psoriasis (TA907)
Psoriasis: assessment and management (CG153)
Baricitinib for treating severe alopecia areata (TA926)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 3 · Randomised trials: 3 · 1975–2026
Showing the 50 most relevant studies, sorted by most relevant.
R. Agarwal, O. Katare, Suresh P. Vyas
International journal of pharmaceutics, 2001
- Drug Delivery Systems
- Administration, Topical
- Anthralin
P. V. D. van de Kerkhof, P. V. D. van der valk, O. Swinkels, et al.
British Journal of Dermatology, 2006
- Anthralin
- Calcitriol
- Day Care, Medical
Lajos Kemény, Thomas Ruzicka, Otto Braun‐Falco
Skin Pharmacology, 2009
- Anthralin
- Psoriasis
Sandy McBride, Patricia Walker, Nick J. Reynolds
British Journal of Dermatology, 2003
- Administration, Topical
- Ambulatory Care
- Anthralin
Dino Vella Briffa, S. Rogers, Malcolm W. Greaves, et al.
Clinical and Experimental Dermatology, 1978
- Photochemotherapy
- Anthracenes
- Anthralin
K. Storbeck, Erhard Hölzle, Nanna Schürer, et al.
Journal of the American Academy of Dermatology, 1993
- Anthralin
- Combined Modality Therapy
- Psoriasis
J. Berth‐Jones, A.C. Chu, W. ALAN DODD, et al.
British Journal of Dermatology, 1992
- Anthralin
- Calcitriol
- Calcium
Pushpendra Kumar Tripathi, Bapi Gorain, Hira Choudhury, et al.
Heliyon, 2019
Priyadarshini Sathe, Raju Saka, Nagavendra Kommineni, et al.
Drug Development and Industrial Pharmacy, 2019
- Imiquimod
- Administration, Cutaneous
- Anthralin
Virendra Sehgal, Prashant Verma, Ananta Khurana
International Journal of Dermatology, 2014
- Anthralin
- Skin Diseases
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
Not available
Mechanism
Anthralin inhibits the proliferation of keratinocytes (epidermal skin cells), pr…
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
[L1932]…
Metabolism
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
This specific property of the molecule inspired workers to study details of its pharmacology. It is important to consider that the drug is relatively innocuous, yet effective, and systemic side effects have not been observed with this anthralin, in contrast to a wide variety of systemic and topical therapies for psoriasis [L1935].
Anthralin is also known as dithranol. It is a main active ingredient in topical skin formulations for the treatment of psoriasis. Various formulations of the drug are available, including solutions, foams, and shampoos [L1979]. The chemical structure of anthralin allows for dual solubility, permitting the compound to be absorbed well through the epidermis [A27276].
Anthralin has also been studied in the treatment of warts, showing promising results [A32307]. Salicylic acid is frequently added to anthralin to augment the stability of anthralin and to increase its penetration and efficacy [L1979].
[L1933]
It is also used topically in the management of psoriasis, dermatoses, and alopecia areata. Anthralin is also used in biomedical research due to its effect on EGFR autophosphorylation .
[L1936]
[L1933]
The most common side effects of anthralin are skin irritation and staining of nearby skin, nails, clothing, and other objects that come in contact with the treated patient. The incidence of irritation of psoriatic/surrounding healthy skin is higher in patients who leave anthralin on the skin without rinsing than in those who use short-contact therapy of 2 hours or less, followed by rinsing .
[L1939]
If the psoriatic plaques are well circumscribed, the surrounding normal skin may be protected by the use of a coating agent such as zinc oxide ointment. Anthralin should be applied cautiously to the face and intertriginous areas due to the risk of severe skin irritation .
[L1979]
There is no current evidence of any long-term anthralin toxicity related either to skin exposure or to systemic issues .
[L1939]
Some long-term studies in mice have demonstrated anthralin to be tumorigenic in mouse skin.
This carcinogenic potential has not been thoroughly evaluated. Tumorigenic and carcinogenic effects of anthralin have not been observed in humans at this time .
[L1932]
Anthralin is classified as FDA pregnancy risk category C drug .
[L1979]
It is not known if anthralin can cause fetal harm when administered during gestation. Because of the lack of evidential human data, anthralin should be used during pregnancy only when clearly required .
[L1933]
Anthralin is believed to normalize the rate of epidermal cell proliferation and keratinization by reducing the mitotic activity of the epidermal hyperplasia in psoriasis [L1979].
Anti-proliferative and anti-inflammatory effects of anthralin have been demonstrated on both psoriatic and healthy skin. The anti-proliferative effects of anthralin are thought to be due to a combination of inhibition of DNA synthesis and its strong reducing properties. The effectiveness of anthralin as an anti-psoriatic agent is partly owed to its ability to promote lipid peroxidation and reduce the concentration of endothelial adhesion molecules, which are found to be elevated in psoriatic patients [L1933], [L1979].
Recent studies suggest that its ability to prevent T-lymphocyte activation and normalize keratinocyte differentiation may occur by a direct effect on mitochondria [A32313].
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L1932]
[L1932], [L1933]
Anthralin does not inhibit hepatic microsomal enzyme activity .
[L1933]
Proteins and enzymes this drug interacts with in the body
PMID:1380918
Associated with keratinocyte activation, proliferation and keratinization .
PMID:12598329
Required for maintenance of corneocytes and keratin filaments in suprabasal keratinocytes in the epidermis of the ear, potentially via moderation of expression and localization of keratins and their partner proteins (By similarity). Plays a role in the establishment of the epidermal barrier on plantar skin (By similarity)
May also participate in ApoER2-specific reelin signaling. Directly, or indirectly, regulates GLUT2 gene expression and beta-cell function. Appears to have a role in cell signaling in mature and developing nerve terminals.
May function as a regulator of vesicle transport, through interactions with the JNK-signaling components and motor proteins. Functions as an anti-apoptotic protein and whose level seems to influence the beta-cell death or survival response. Acts as a scaffold protein that coordinates with SH3RF1 in organizing different components of the JNK pathway, including RAC1 or RAC2, MAP3K11/MLK3 or MAP3K7/TAK1, MAP2K7/MKK7, MAPK8/JNK1 and/or MAPK9/JNK2 into a functional multiprotein complex to ensure the effective activation of the JNK signaling pathway.
Regulates the activation of MAPK8/JNK1 and differentiation of CD8(+) T-cells
ATC D05AC01
ATC D05AC51
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Show
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Anthralin
Matched from: Dithranol
Additional database identifiers
Drugs Product Database (DPD)
9362
ChemSpider
2117
BindingDB
50041802
ZINC
ZINC000000001322
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6439
GeneCards
KRT2
UniProt Accession
K22E_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6414
GeneCards
KRT12
UniProt Accession
K1C12_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6882
GeneCards
MAPK8IP1
GenBank Gene Database
AF074091
GenBank Protein Database
4426597
UniProt Accession
JIP1_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
Show earlier publications
Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q419397), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.