U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H8O4
Molecular Weight 216.1895
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHOXSALEN

SMILES

COC1=C2OC(=O)C=CC2=CC3=C1OC=C3

InChI

InChIKey=QXKHYNVANLEOEG-UHFFFAOYSA-N
InChI=1S/C12H8O4/c1-14-12-10-8(4-5-15-10)6-7-2-3-9(13)16-11(7)12/h2-6H,1H3

HIDE SMILES / InChI

Molecular Formula C12H8O4
Molecular Weight 216.1895
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: http://www.drugbank.ca/drugs/DB00553 https://en.wikipedia.org/wiki/Methoxsalen

Methoxsalen — also called xanthotoxin, marketed under the trade names Oxsoralen, Deltasoralen, Meladinine — is a drug used to treat psoriasis, eczema, vitiligo, and some cutaneous lymphomas in conjunction with exposing the skin to UVA light from lamps or sunlight. Methoxsalen modifies the way skin cells receive the UVA radiation, allegedly clearing up the disease. The dosage comes in 10 mg tablets, which are taken in the amount of 30 mg 75 minutes before a PUVA (psoralen + UVA) light treatment. Chemically, methoxsalen belongs to a class of organic natural molecules known as furanocoumarins. They consist of coumarin annulated with furan. It can also be injected and used topically. The exact mechanism of action of methoxsalen with the epidermal melanocytes and keratinocytes is not known. The best known biochemical reaction of methoxsalen is with DNA. Methoxsalen, upon photoactivation, conjugates and forms covalent bonds with DNA which leads to the formation of both monofunctional (addition to a single strand of DNA) and bifunctional adducts (crosslinking of psoralen to both strands of DNA) Reactions with proteins have also been described. Methoxsalen acts as a photosensitizer. Administration of the drug and subsequent exposure to UVA can lead to cell injury. Orally administered methoxsalen reaches the skin via the blood and UVA penetrates well into the skin. If sufficient cell injury occurs in the skin, an inflammatory reaction occurs. The most obvious manifestation of this reaction is delayed erythema, which may not begin for several hours and peaks at 48–72 hours. The inflammation is followed, over several days to weeks, by repair which is manifested by increased melanization of the epidermis and thickening of the stratum corneum. The mechanisms of therapy are not known. In the treatment of vitiligo, it has been suggested that melanocytes in the hair follicle are stimulated to move up the follicle and to repopulate the epidermis. In the treatment of psoriasis, the mechanism is most often assumed to be DNA photodamage and resulting decrease in cell proliferation but other vascular, leukocyte, or cell regulatory mechanisms may also be playing some role. Psoriasis is a hyperproliferative disorder and other agents known to be therapeutic for psoriasis are known to inhibit DNA synthesis. The most commonly reported side effect of methoxsalen alone is nausea, which occurs with approximately 10% of all patients. This effect may be minimized or avoided by instructing the patient to take methoxsalen with milk or food, or to divide the dose into two portions, taken approximately one-half hour apart. Other effects include nervousness, insomnia, and psychological depression.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
8-MOP

Approved Use

when the diagnosis has been supported by biopsy. Photochemotherapy is intended to be administered only in conjunction with a schedule of controlled doses of long wave ultraviolet radiation.

Launch Date

1954
Primary
8-MOP

Approved Use

Photochemotherapy (methoxsalen with long wave ultraviolet radiation) is indicated for the repigmentation of idiopathic vitiligo

Launch Date

1954
Palliative
8-MOP

Approved Use

in the palliative treatment of the skin manifestations of cutaneous T-cell lymphoma (CTCL) in persons who have not been responsive to other forms of treatment. While this dosage form of methoxsalen has been approved for use in combination with photopheresis, Oxsoralen Ultra Capsules have not been approved for that use.

Launch Date

1954
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
127.63 ng/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
125.16 ng/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
155 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN serum
Homo sapiens
population: UNHEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
129 ng/mL
0.6 mg/kg single, oral
dose: 0.6 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
335.48 ng × h/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
321.25 ng × h/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
420 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN serum
Homo sapiens
population: UNHEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
521 ng × h/mL
0.6 mg/kg single, oral
dose: 0.6 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
61 min
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN serum
Homo sapiens
population: UNHEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
2.38 h
0.6 mg/kg single, oral
dose: 0.6 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXSALEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
0.6 mg/kg 4 times / week multiple, oral
Recommended
Dose: 0.6 mg/kg, 4 times / week
Route: oral
Route: multiple
Dose: 0.6 mg/kg, 4 times / week
Sources:
unhealthy, 49.7
Health Status: unhealthy
Age Group: 49.7
Sex: M+F
Sources:
70 mg 4 times / week multiple, oral
Recommended
Dose: 70 mg, 4 times / week
Route: oral
Route: multiple
Dose: 70 mg, 4 times / week
Sources:
unhealthy
Disc. AE: Cataract...
AEs leading to
discontinuation/dose reduction:
Cataract
Sources:
AEs

AEs

AESignificanceDosePopulation
Cataract Disc. AE
70 mg 4 times / week multiple, oral
Recommended
Dose: 70 mg, 4 times / week
Route: oral
Route: multiple
Dose: 70 mg, 4 times / week
Sources:
unhealthy
OverviewDrug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no
yes [IC50 2 uM]
yes [Ki 0.11 uM]
yes [Ki 0.2 uM]
yes [Ki 0.8 uM]
yes [Ki 20 uM]
yes [Ki 20 uM]
yes [Ki 25 uM]
yes [Ki 3 uM]
yes [Ki 35 uM]
yes [Ki 75 uM]
yes
yes
yes
Drug as victim

Drug as victim

Tox targets
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
In vivo effect of 5- and 8-methoxypsoralens and cimetidine on R,S-warfarin metabolism in rat.
2002-10-02
DNA cross-link-dependent RAD50/MRE11/NBS1 subnuclear assembly requires the Fanconi anemia C protein.
2002-10-01
Phytochemical and pharmacological studies on Sideritis taurica Stephan ex Wild.
2002-10
Tea: not immoral, illegal, or fattening, but is it innocuous?
2002-09-14
Epoxidation of some natural furocoumarins and furochromones using gamma-ray.
2002-08-29
Oral administration of 5-methoxypsoralen affects the distribution and metabolism of 2-aminofluorene in Sprague-Dawley rats.
2002-08-17
Changes in skin physiology during bath PUVA therapy.
2002-07
Can a mixed damage interfere with DNA-protein cross-links repair?
2002-06-18
A melanocyte-keratinocyte coculture model to assess regulators of pigmentation in vitro.
2002-06-15
Extracorporeal photochemotherapy: a new therapeutic approach for allograft rejection.
2002-06
T cell clonality and the effect of photopheresis in systemic sclerosis and graft versus host disease.
2002-06
Transimmunization and the evolution of extracorporeal photochemotherapy.
2002-06
Severe influenzalike symptoms associated with methoxsalen photochemotherapy.
2002-06
Synthesis, photobiological activity and photoreactivity of methyl-thieno-8-azacoumarins, novel bioisosters of psoralen.
2002-05-06
3-Alkyl- and 3-aryl-7H-furo[3,2-g]-1-benzopyran-7-ones: synthesis, photoreactivity, and fluorescence properties.
2002-05
Differential effect of 8-methoxypsoralen, 4,6,4'-trimethylangelicin, and chlorpromazine on cell death and TNF-alpha production.
2002-05
Werner syndrome diploid fibroblasts are sensitive to 4-nitroquinoline-N-oxide and 8-methoxypsoralen: implications for the disease phenotype.
2002-05
p53 and Fas ligand are required for psoralen and UVA-induced apoptosis in mouse epidermal cells.
2002-05
Studies on mechanism of 8-methoxypsoralen-DNA interaction in the dark.
2002-04-26
Effects of storage conditions on furocoumarin levels in intact, chopped, or homogenized parsnips.
2002-04-24
Amino acids in SRS1 and SRS6 are critical for furanocoumarin metabolism by CYP6B1v1, a cytochrome P450 monooxygenase.
2002-04
Chalcones and other constituents of Dorstenia prorepens and Dorstenia zenkeri.
2002-04
Simultaneous determination of furanocoumarins in infusions and decoctions from "Carapiá" (dorstenia species) by high-performance liquid chromatography.
2002-03-13
Time course of 8-methoxypsoralen concentrations in skin and plasma after topical (bath and cream) and oral administration of 8-methoxypsoralen.
2002-03
Decreased survival of UV-irradiated Staphylococcus aureus in the presence of 8-methoxypsoralen in the post-irradiation plating medium.
2002-03
Bullous phytophotodermatitis associated with high natural concentrations of furanocoumarins in limes.
2002-03
Novel angular furo and thieno-quinolinones: synthesis and preliminary photobiological studies.
2002-03
Synthesis and biological evaluation of a new furo[2,3-h]quinolin-2(1H)-one.
2002-02-28
[Acute generalized exanthematous pustulosis due to meladinine with positive patch tests].
2002-02
Mitochondrial alterations in fanconi anemia fibroblasts following ultraviolet A or psoralen photoactivation.
2002-02
Effects of the isoflavone 4',5,7-trihydroxyisoflavone (genistein) on psoralen plus ultraviolet A radiation (PUVA)-induced photodamage.
2002-02
Cell-impermeant pyridinium derivatives of psoralens as inhibitors of keratinocyte growth.
2002-01-01
Evaluation of synergism in the feeding deterrence of some furanocoumarins on Spodoptera littoralis.
2002-01
Extracorporeal photopheresis in cutaneous T-cell lymphoma and graft-versus-host disease induces both immediate and progressive apoptotic processes.
2002-01
Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.
2002-01
Photoclastogenicity-an improved protocol, its validation, and investigation of the photogenotoxicity of DMBA.
2002
Can the immersion time of PUVA bath therapy be shortened?
2002
Characteristics of photopheresis treatments for the management of rejection in heart and lung transplant recipients.
2002
S. cerevisiae has three pathways for DNA interstrand crosslink repair.
2001-12-19
Developmental variation in cytochrome P450 expression in Papilio polyxenes in response to xanthotoxin, a hostplant allelochemical.
2001-12
Photosensitization and mutation induced in Escherichia coli and Saccharomyces cerevisiae strains by dorstenin, a psoralen analog isolated from Dorstenia bahiensis.
2001-12
Systemic allergic contact dermatitis to 8-methoxypsoralen (8-MOP).
2001-12
Induction of apoptosis, depletion of glutathione, and DNA damage by extracorporeal photochemotherapy and psoralen with exposure to UV light in vitro.
2001-11-29
PUVA downregulates whn expression in primary mouse keratinocytes.
2001-11-01
Anaphylaxis to 5-methoxypsoralen during photochemotherapy.
2001-11
Acitretin therapy for palmoplantar pustulosis combined with UVA and topical 8-MOP.
2001-08
Localized vitiligo successfully treated with cream-psoralen + ultraviolet A.
2001-07
What's new in the treatment of vitiligo.
2001-07
Assessment of the phototoxic potential of compounds and finished topical products using a human reconstructed epidermis.
2001
Serum folate levels after UVA exposure: a two-group parallel randomised controlled trial.
2001
Patents

Sample Use Guides

VITILIGO THERAPY : Two capsules (10 mg each) in one dose taken with milk or in food two to four hours before ultraviolet light exposure. PSORIASIS THERAPY: The methoxsalen capsules should be taken 2 hours before UVA exposure with some food or milk
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: 8-Methoxypsoralen was assessed for its effects on in vitro lymphocyte proliferation in the absence of ultraviolet radiation. 8-Methoxypsoralen inhibited both the phytohemagglutinin and concanavalin A-induced proliferation of normal human peripheral blood lymphocytes in a time and dose-dependent manner.
8-Methoxypsoralen inhibited both the phytohemagglutinin and concanavalin A-induced proliferation of normal human peripheral blood lymphocytes in a time and dose-dependent manner.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:45:47 GMT 2025
Edited
by admin
on Mon Mar 31 17:45:47 GMT 2025
Record UNII
U4VJ29L7BQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHOXSALEN
HSDB   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
Common Name English
8-MOP
Preferred Name English
VITPSO
Common Name English
METHOXSALEN [HSDB]
Common Name English
NSC-45923
Code English
XANTHOTOXIN
Common Name English
METHOXSALEN [USP MONOGRAPH]
Common Name English
SM-88 COMPONENT METHOXSALEN
Code English
8-METHOXYPSORALEN
Common Name English
OXYPSORALEN
Common Name English
METHOXSALEN [USP-RS]
Common Name English
METHOXSALEN [ORANGE BOOK]
Common Name English
METHOXSALEN [JAN]
Common Name English
Methoxsalen [WHO-DD]
Common Name English
9-Methoxy-7H-furo[3,2-g][1]benzopyran-7-one
Systematic Name English
METHOXSALEN [MART.]
Common Name English
UVADEX
Brand Name English
7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 9-METHOXY-
Systematic Name English
OXSORALEN
Brand Name English
METHOXSALEN [VANDF]
Common Name English
PUVALEN
Common Name English
METHOXSALEN [IARC]
Common Name English
8-METHOXSALEN
Common Name English
METHOXSALEN [MI]
Common Name English
METOXALEN
Common Name English
Classification Tree Code System Code
NDF-RT N0000010217
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
WHO-ATC D05AD02
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
WHO-ATC D05BA02
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NDF-RT N0000007909
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
EU-Orphan Drug EU/3/06/374
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
WHO-VATC QD05AD02
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
FDA ORPHAN DRUG 80594
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NCI_THESAURUS C1420
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NDF-RT N0000007909
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
FDA ORPHAN DRUG 117298
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NDF-RT N0000009801
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NCI_THESAURUS C25760
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
WHO-VATC QD05BA02
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NDF-RT N0000175879
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
NDF-RT N0000007909
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
FDA ORPHAN DRUG 74293
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
LIVERTOX 620
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NDF-RT N0000175984
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
Code System Code Type Description
DRUG CENTRAL
30
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
MERCK INDEX
m7329
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY Merck Index
CAS
298-81-7
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
HSDB
2505
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
MESH
D008730
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PRIMARY
RS_ITEM_NUM
1417001
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PRIMARY
SMS_ID
100000092592
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
RXCUI
6854
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY RxNorm
WIKIPEDIA
METHOXSALEN
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
FDA UNII
U4VJ29L7BQ
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
DRUG BANK
DB00553
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
PUBCHEM
4114
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
CHEBI
18358
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-066-9
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
NSC
45923
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
NCI_THESAURUS
C643
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
DAILYMED
U4VJ29L7BQ
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
ChEMBL
CHEMBL416
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
EPA CompTox
DTXSID8020830
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
LACTMED
Methoxsalen
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
EVMPD
SUB14541MIG
Created by admin on Mon Mar 31 17:45:47 GMT 2025 , Edited by admin on Mon Mar 31 17:45:47 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
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PARENT -> CONSTITUENT ALWAYS PRESENT
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IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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IMPURITY -> PARENT
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ACTIVE MOIETY