Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H12N2O2S |
| Molecular Weight | 248.301 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(N)C=C2
InChI
InChIKey=MQJKPEGWNLWLTK-UHFFFAOYSA-N
InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2
| Molecular Formula | C12H12N2O2S |
| Molecular Weight | 248.301 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://escholarship.org/uc/item/30m4b5krCurator's Comment: description was created based on several sources, including http://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021794s000_MicroR.pdf
Sources: http://escholarship.org/uc/item/30m4b5kr
Curator's Comment: description was created based on several sources, including http://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021794s000_MicroR.pdf
Dapsone was synthesized in 1908 by Fromm and Wittmann. The drug was approved by FDA for the treatment of such conditions as acne vulgaris, leprosy and dermatitis herpetiformis, also the drug is used off-label for many skin diseases. Although the exact mechanism of dapsone action is unknown, it is speculated that it acts as both anti-inflammatory and antimicrobial agent. It was demonstrated that dapsone suppresses ROS generation, inhibits neutrophil myeloperoxidase and eosinophil peroxidase and also inhibits bacterial dihydropteroate synthase.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2364668 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24310318 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | ACZONE Approved UseGel is indicated for the topical treatment of acne vulgaris. Launch Date1955 |
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| Curative | DAPSONE Approved UseDermatitis herpetiformis: (D.H.) Leprosy: All forms of leprosy except for cases of proven Dapsone resistance. Launch Date1979 |
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| Curative | DAPSONE Approved UseDermatitis herpetiformis: (D.H.) Leprosy: All forms of leprosy except for cases of proven Dapsone resistance. Launch Date1979 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
19.7 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
110 mg 2 times / day steady-state, topical dose: 110 mg route of administration: Topical experiment type: STEADY-STATE co-administered: |
DAPSONE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1375 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
DAPSONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
415 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
110 mg 2 times / day steady-state, topical dose: 110 mg route of administration: Topical experiment type: STEADY-STATE co-administered: |
DAPSONE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
22783 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
DAPSONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
52641 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
DAPSONE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
221.52 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
110 mg 2 times / day steady-state, topical dose: 110 mg route of administration: Topical experiment type: STEADY-STATE co-administered: |
DAPSONE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
42 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
110 mg 2 times / day steady-state, topical dose: 110 mg route of administration: Topical experiment type: STEADY-STATE co-administered: |
DAPSONE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
20.6 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17655376 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
DAPSONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
10% |
unknown, unknown |
DAPSONE plasma | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
300 mg 1 times / week multiple, oral Highest studied dose Dose: 300 mg, 1 times / week Route: oral Route: multiple Dose: 300 mg, 1 times / week Sources: |
unhealthy, 38 |
Disc. AE: Anemia, Rash... AEs leading to discontinuation/dose reduction: Anemia (11.1%) Sources: Rash (11.1%) Fever (11.1%) |
200 mg 1 times / week multiple, oral MTD Dose: 200 mg, 1 times / week Route: oral Route: multiple Dose: 200 mg, 1 times / week Sources: |
unhealthy, 38 |
Disc. AE: Vomiting, Fever... AEs leading to discontinuation/dose reduction: Vomiting (14.3%) Sources: Fever (14.3%) |
10 g single, oral Overdose |
unhealthy, 45 |
Disc. AE: Cyanosis, Methaemoglobinaemia... AEs leading to discontinuation/dose reduction: Cyanosis (acute) Sources: Methaemoglobinaemia Haemolysis |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Anemia | 11.1% Disc. AE |
300 mg 1 times / week multiple, oral Highest studied dose Dose: 300 mg, 1 times / week Route: oral Route: multiple Dose: 300 mg, 1 times / week Sources: |
unhealthy, 38 |
| Fever | 11.1% Disc. AE |
300 mg 1 times / week multiple, oral Highest studied dose Dose: 300 mg, 1 times / week Route: oral Route: multiple Dose: 300 mg, 1 times / week Sources: |
unhealthy, 38 |
| Rash | 11.1% Disc. AE |
300 mg 1 times / week multiple, oral Highest studied dose Dose: 300 mg, 1 times / week Route: oral Route: multiple Dose: 300 mg, 1 times / week Sources: |
unhealthy, 38 |
| Fever | 14.3% Disc. AE |
200 mg 1 times / week multiple, oral MTD Dose: 200 mg, 1 times / week Route: oral Route: multiple Dose: 200 mg, 1 times / week Sources: |
unhealthy, 38 |
| Vomiting | 14.3% Disc. AE |
200 mg 1 times / week multiple, oral MTD Dose: 200 mg, 1 times / week Route: oral Route: multiple Dose: 200 mg, 1 times / week Sources: |
unhealthy, 38 |
| Haemolysis | Disc. AE | 10 g single, oral Overdose |
unhealthy, 45 |
| Methaemoglobinaemia | Disc. AE | 10 g single, oral Overdose |
unhealthy, 45 |
| Cyanosis | acute Disc. AE |
10 g single, oral Overdose |
unhealthy, 45 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Establishment of knockdown of superoxide dismutase 2 and expression of CYP3A4 cell system to evaluate drug-induced cytotoxicity. | 2009-09 |
|
| Complete atrioventricular block associated with dapsone therapy: a rare complication of dapsone-induced hypersensitivity syndrome. | 2009-08 |
|
| Representation of time-varying stimuli by a network exhibiting oscillations on a faster time scale. | 2009-05 |
|
| Complex phase separation in poly(acrylonitrile-butadiene-styrene)-modified epoxy/4,4'-diaminodiphenyl sulfone blends: generation of new micro- and nanosubstructures. | 2009-04-23 |
|
| Synthesis and characterization of new optically active poly(azo-ester-imide)s via interfacial polycondensation. | 2009-03 |
|
| Dapsone-induced haemolytic anaemia, hepatitis and agranulocytosis in a leprosy patient with normal glucose-6-phosphate-dehydrogenase activity. | 2008-12 |
|
| Antioxidant, antiinflammatory and antiapoptotic effects of dapsone in a model of brain ischemia/reperfusion in rats. | 2008-11-15 |
|
| Dapsone-induced hemolytic anemia in lung allograft recipients. | 2008-11 |
|
| A possible inhibitory action of diaminodiphenyl sulfone on tumour necrosis factor-alpha production from activated mononuclear cells on cutaneous lupus erythematosus. | 2008-11 |
|
| The processing of English regular inflections: Phonological cues to morphological structure. | 2008-10 |
|
| Dapsone induces oxidative stress and impairs antioxidant defenses in rat liver. | 2008-08-01 |
|
| A novel assay system for myeloperoxidase activity in whole saliva. | 2008-05 |
|
| Open-label comparative clinical study of chlorproguanil-dapsone fixed dose combination (Lapdap) alone or with three different doses of artesunate for uncomplicated Plasmodium falciparum malaria. | 2008-03-05 |
|
| [A case of relapsing polychondritis monitored by repeated measurements of flow-volume curve]. | 2008-03 |
|
| Beneficial effects of word final stress in segmenting a new language: evidence from ERPs. | 2008-02-18 |
|
| High risk of severe anaemia after chlorproguanil-dapsone+artesunate antimalarial treatment in patients with G6PD (A-) deficiency. | 2008 |
|
| Anti-inflammatory and immune therapy for Alzheimer's disease: current status and future directions. | 2007-12 |
|
| [Long-term follow-up of ofloxacin-combined therapy for leprosy patients]. | 2007-09 |
|
| Consultative meeting to develop a strategy for treatment of cutaneous leishmaniasis. Institute Pasteur, Paris. 13-15 June, 2006. | 2007-04-24 |
|
| Neuroprotective effect of dapsone in patients with acute ischemic stroke: a pilot study. | 2007-04 |
|
| [Disulone and hepatosiderosis]. | 2006-10-21 |
|
| The sulfone syndrome secondary to dapsone prophylaxis in a patient undergoing unrelated hematopoietic stem cell transplantation. | 2006-09 |
|
| Anterior ischaemic optic neuropathy associated with Dapsone. | 2006-08 |
|
| The Dapsone hypersensitivity syndrome revisited: a potentially fatal multisystem disorder with prominent hepatopulmonary manifestations. | 2006-06-06 |
|
| Acute methemoglobinemia following attempted suicide by Dapson. | 2006-04 |
|
| Guillain-Barré syndrome-like presentation in borderline leprosy with type-2 reaction. | 2006-02-28 |
|
| Role of human cyclooxygenase-2 in the bioactivation of dapsone and sulfamethoxazole. | 2006-01 |
|
| [Refractory cutaneous necrotizing vasculitis. Successful sulfone therapy]. | 2006-01 |
|
| The contribution of prosody to the perception of foreign accent. | 2006 |
|
| Differential antibiotic susceptibilities of starved Mycobacterium tuberculosis isolates. | 2005-11 |
|
| Complications related to dapsone use for Pneumocystis jirovecii pneumonia prophylaxis in solid organ transplant recipients. | 2005-11 |
|
| Childhood bullous pemphigoid successfully treated with diaminodiphenyl sulfone. | 2005-10 |
|
| Robust acoustic object detection. | 2005-10 |
|
| A case of drug-induced hypersensitivity syndrome with multiple organ involvement treated with plasma exchange. | 2005-10 |
|
| Renal hypersensitivity vasculitis associated with dapsone. | 2005-10 |
|
| Protective role of vitamin E on the oxidative stress in Hansen's disease (Leprosy) patients. | 2005-10 |
|
| Dapsone impairs the bile salt-independent fraction of bile flow in rats: Possible involvement of its N-hydroxylated metabolite. | 2005-07-01 |
|
| [Dapsone-induced agranulocytosis. The role of xenobiotic-metabolizing enzymes demonstrated by a case report]. | 2005-07 |
|
| Aplastic anaemia associated with multidrug therapy (dapsone, rifampicin and clofazimine) in a patient with lepromatous leprosy. | 2005-06 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| Dapsone suppresses human neutrophil superoxide production and elastase release in a calcium-dependent manner. | 2005-05 |
|
| Dapsone syndrome with acute renal failure during leprosy treatment: case report. | 2005-02 |
|
| Relationships between nonword repetition accuracy and other measures of linguistic development in children with phonological disorders. | 2005-02 |
|
| Simultaneous determination of beta-blocking agents and diuretics in doping analysis by liquid chromatography/mass spectrometry with scan-to-scan polarity switching. | 2005 |
|
| [Disulone]. | 2004-12 |
|
| Dapsone suppresses integrin-mediated neutrophil adherence function. | 1992-02 |
|
| [Granulomatous hepatitis caused by dapsone]. | 1992 |
|
| [Polyneuropathy in Duhring dermatitis herpetiformis]. | 1991-08 |
|
| Dapsone-induced peripheral neuropathy. | 1976-12 |
|
| Dapsone-induced motor polyneuropathy. A complication of prolonged treatment of subcorneal pustular dermatosis. | 1976-08 |
Patents
Sample Use Guides
In Vivo Use Guide
Curator's Comment: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7fc98c9b-b17a-f66f-055b-259207ad9504
Apply 5% gel to the acne affected areas twice a day (Aczone gel). In dermatitis herpetiformis, the starting oral dose is 50 mg and in leprosy, the dose is 100 mg/day (Dapsone oral formulation).
Route of Administration:
Other
With Staphylococcus aureus (both methicillin-susceptible S. aureus-MSSA and methicillinresistant S. aureus-MRSA), dapsone MIC50, MIC90 were 128 ug/mL and 256 ug/mL, respectively. For Staphylococcus epidermidis overall, dapsone MIC50, MIC90 were 128 ug/mL and 256 ug/mL, respectively. Overall results with Enterococcus faecalis, dapsone MIC50, MIC90 were 256 ug/mL and 512 ug/mL, respectively. With Streptococcus agalactiae, dapsone MIC50, MIC90 were reported overall to be 32 ug/mL and 256 ug/mL, respectively. For Streptococcus pyogenes, dapsone MIC50, MIC90 were 32 ug/mL and 512 ug/mL, respectively.
| Substance Class |
Chemical
Created
by
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on
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| Record UNII |
8W5C518302
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Validated (UNII)
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| Classification Tree | Code System | Code | ||
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NDF-RT |
N0000008053
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NCI_THESAURUS |
C849
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WHO-VATC |
QD10AX05
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WHO-ESSENTIAL MEDICINES LIST |
6.2.3
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WHO-ATC |
J04BA02
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WHO-VATC |
QJ04BA02
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WHO-ATC |
D10AX05
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FDA ORPHAN DRUG |
85694
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NDF-RT |
N0000175881
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NDF-RT |
N0000008053
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FDA ORPHAN DRUG |
61291
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EPA PESTICIDE CODE |
690107
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LIVERTOX |
NBK548936
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FDA ORPHAN DRUG |
61191
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5073
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D003622
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SUB06909MIG
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3108
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782
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201-248-4
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m4092
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100000083461
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1164008
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DAPSONE
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PRIMARY | Description: A white or creamy white, crystalline powder; odourless. Solubility: Soluble in 7000 parts of water and in 30 parts of ethanol (~750 g/l) TS; soluble in acetone R.Category: Antileprotic. Storage: Dapsone should be kept in a tightly closed container, protected from light. Additional information: Even in the absence of light, Dapsone is gradually degraded on exposure to a humid atmosphere, thedecomposition being faster at higher temperatures. | ||
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DAPSONE
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Dapsone
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DB00250
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6091
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C415
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DTXSID4020371
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METABOLIC ENZYME -> SUBSTRATE |
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METABOLIC ENZYME -> SUBSTRATE | |||
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METABOLITE -> PARENT |
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PARENT -> METABOLITE |
We have also shown recently that greater than 90% of dapsone hydroxylation in human liver microsomes is undertaken by cytochrome P4503A4
URINE
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METABOLITE -> PARENT |
PLASMA
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METABOLITE TOXIC -> PARENT |
Metabolite known for methaemoglobin formation in man.
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METABOLITE -> PARENT |
URINE
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IMPURITY -> PARENT |
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CHROMATOGRAPHIC PURITY (HPLC/UV)
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ACTIVE MOIETY |
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