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Details

Stereochemistry ACHIRAL
Molecular Formula C17H22N4O2
Molecular Weight 314.3822
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RESIQUIMOD

SMILES

CCOCC1=NC2=C(N1CC(C)(C)O)C3=C(C=CC=C3)N=C2N

InChI

InChIKey=BXNMTOQRYBFHNZ-UHFFFAOYSA-N
InChI=1S/C17H22N4O2/c1-4-23-9-13-20-14-15(21(13)10-17(2,3)22)11-7-5-6-8-12(11)19-16(14)18/h5-8,22H,4,9-10H2,1-3H3,(H2,18,19)

HIDE SMILES / InChI

Molecular Formula C17H22N4O2
Molecular Weight 314.3822
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://en.pharmacodia.com/web/drug/1_983.html | https://www.ncbi.nlm.nih.gov/pubmed/19841637

Resiquimod is an imidazoquinolinamine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through the TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages, and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activation of other transcription factors. This may lead to an increase in mRNA levels and subsequent production of cytokines, especially interferon-alpha (INF-a) and other cytokines, thereby enhancing T-helper 1 (Th1) immune responses. In addition, topical application of resiquimod appears to activate Langerhans' cells, leading to an enhanced activation of T-lymphocytes. Resiquimod is used as a topical gel[1] in the treatment of skin lesions[2] such as those caused by the herpes simplex virus[3][4] and cutaneous T cell lymphoma. Due to its immunostimulatory activity, this agent may potentially be used as a vaccine adjuvant.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
3.82 ng/mL
0.01 mg/kg single, oral
dose: 0.01 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
RESIQUIMOD plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
7.55 ng/mL
0.02 mg/kg single, oral
dose: 0.02 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
RESIQUIMOD plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
45.66 ng × h/mL
0.02 mg/kg single, oral
dose: 0.02 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
RESIQUIMOD plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
6.82 h
0.02 mg/kg single, oral
dose: 0.02 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
RESIQUIMOD plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
0.02 mg/kg 2 times / week multiple, oral
Highest studied dose
Dose: 0.02 mg/kg, 2 times / week
Route: oral
Route: multiple
Dose: 0.02 mg/kg, 2 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Lymphopenia, Lymphopenia...
AEs leading to
discontinuation/dose reduction:
Lymphopenia (grade 3, 9%)
Lymphopenia (grade 3, 9%)
Flu-like symptoms (grade 3, 9%)
Sources:
0.1 % 3 times / week multiple, topical
Studied dose
Dose: 0.1 %, 3 times / week
Route: topical
Route: multiple
Dose: 0.1 %, 3 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Localized skin reaction...
AEs leading to
discontinuation/dose reduction:
Localized skin reaction
Sources:
AEs

AEs

AESignificanceDosePopulation
Flu-like symptoms grade 3, 9%
Disc. AE
0.02 mg/kg 2 times / week multiple, oral
Highest studied dose
Dose: 0.02 mg/kg, 2 times / week
Route: oral
Route: multiple
Dose: 0.02 mg/kg, 2 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Lymphopenia grade 3, 9%
Disc. AE
0.02 mg/kg 2 times / week multiple, oral
Highest studied dose
Dose: 0.02 mg/kg, 2 times / week
Route: oral
Route: multiple
Dose: 0.02 mg/kg, 2 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Lymphopenia grade 3, 9%
Disc. AE
0.02 mg/kg 2 times / week multiple, oral
Highest studied dose
Dose: 0.02 mg/kg, 2 times / week
Route: oral
Route: multiple
Dose: 0.02 mg/kg, 2 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Localized skin reaction Disc. AE
0.1 % 3 times / week multiple, topical
Studied dose
Dose: 0.1 %, 3 times / week
Route: topical
Route: multiple
Dose: 0.1 %, 3 times / week
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Selective inhibition of the NLRP3 inflammasome by targeting to promyelocytic leukemia protein in mouse and human.
2013-04-18
A critical role for MAPK signalling pathways in the transcriptional regulation of toll like receptors.
2013
Tetra-O-methyl nordihydroguaiaretic acid (Terameprocol) inhibits the NF-κB-dependent transcription of TNF-α and MCP-1/CCL2 genes by preventing RelA from binding its cognate sites on DNA.
2010-12-07
An intranasally delivered Toll-like receptor 7 agonist elicits robust systemic and mucosal responses to Norwalk virus-like particles.
2010-12
Inhibition of the type I interferon antiviral response during arenavirus infection.
2010-11
Cellular and molecular mechanisms underlying the strong neonatal IL-12 response of lamb mesenteric lymph node cells to R-848.
2010-10-28
Protective effects of Sm-p80 in the presence of resiquimod as an adjuvant against challenge infection with Schistosoma mansoni in mice.
2010-09
TLR8 agonists stimulate newly recruited monocyte-derived cells into potent APCs that enhance HBsAg immunogenicity.
2010-08-31
Herpes simplex virus and human papillomavirus genital infections: new and investigational therapeutic options.
2010-07
Dendritic cells in uninfected infants born to hepatitis B virus-positive mothers.
2010-07
2,3,7,8-tetrachlorodibenzo-p-dioxin-mediated suppression of toll-like receptor stimulated B-lymphocyte activation and initiation of plasmacytic differentiation.
2010-07
Immune mechanisms of protection: can adjuvants rise to the challenge?
2010-04-12
Topical resiquimod: a promising adjuvant for vaccine development?
2010-01
The Toll-like receptor 7/8 agonist resiquimod greatly increases the immunostimulatory capacity of human acute myeloid leukemia cells.
2010-01
Targeting Toll-like receptors for treatment of SLE.
2010
Toll-like receptors: role in dermatological disease.
2010
Molecular modulation of intestinal epithelial barrier: contribution of microbiota.
2010
Short-term cultured, interleukin-15 differentiated dendritic cells have potent immunostimulatory properties.
2009-12-18
Pharmacotherapy of actinic keratosis.
2009-12
Toward the discovery of vaccine adjuvants: coupling in silico screening and in vitro analysis of antagonist binding to human and mouse CCR4 receptors.
2009-11-30
Growth inhibition of thyroid follicular cell-derived cancers by the opioid growth factor (OGF) - opioid growth factor receptor (OGFr) axis.
2009-10-18
Nanoparticle-delivered multimeric soluble CD40L DNA combined with Toll-Like Receptor agonists as a treatment for melanoma.
2009-10-08
Topical resiquimod promotes priming of CTL to parenteral antigens.
2009-09-25
Modulation of the allergic asthma transcriptome following resiquimod treatment.
2009-08-07
Sequence determinants of innate immune activation by short interfering RNAs.
2009-07-24
Oxidative stress augments toll-like receptor 8 mediated neutrophilic responses in healthy subjects.
2009-06-15
Do postsurgical interventions optimize ultimate scar cosmesis.
2009-06
Rectal and vaginal immunization of mice with human papillomavirus L1 virus-like particles.
2009-04-14
Reversal of human papillomavirus-specific T cell immune suppression through TLR agonist treatment of Langerhans cells exposed to human papillomavirus type 16.
2009-03-01
Expression and activity of Toll-like receptors 1-9 in the human term placenta and changes associated with labor at term.
2009-02
Toll-like receptor 7-induced naive human B-cell differentiation and immunoglobulin production.
2009-01
TLR7 and TLR8 ligands and antiphospholipid antibodies show synergistic effects on the induction of IL-1beta and caspase-1 in monocytes and dendritic cells.
2009
Hepatitis C virus is a weak inducer of interferon alpha in plasmacytoid dendritic cells in comparison with influenza and human herpesvirus type-1.
2009
Imiquimod upregulates the opioid growth factor receptor to inhibit cell proliferation independent of immune function.
2008-08
Comparison of human B cell activation by TLR7 and TLR9 agonists.
2008-07-24
A phase II dose-ranging study of topical resiquimod to treat actinic keratosis.
2008-07
Differential regulation of interleukin 12 and interleukin 23 production in human dendritic cells.
2008-06-09
Intra-colonic administration of the TLR7 agonist R-848 induces an acute local and systemic inflammation in mice.
2008-03-07
TLR7 and TLR8 as targets in cancer therapy.
2008-01-07
Toll-like receptors and viruses: induction of innate antiviral immune responses.
2008
Primary prevention of allergic diseases: current concepts and mechanisms.
2007-12-15
HIV-1/HSV-2 co-infected adults in early HIV-1 infection have elevated CD4+ T cell counts.
2007-10-24
Transcriptional networks in plasmacytoid dendritic cells stimulated with synthetic TLR 7 agonists.
2007-10-12
Resiquimod and other immune response modifiers as vaccine adjuvants.
2007-10
TLR agonists induce the differentiation of human bone marrow CD34+ progenitors into CD11c+ CD80/86+ DC capable of inducing a Th1-type response.
2007-10
Impaired CCR7 expression on plasmacytoid dendritic cells of HIV-infected children and adolescents with immunologic and virologic failure.
2007-08-15
Oral resiquimod in chronic HCV infection: safety and efficacy in 2 placebo-controlled, double-blind phase IIa studies.
2007-08
Topical resiquimod 0.01% gel decreases herpes simplex virus type 2 genital shedding: a randomized, controlled trial.
2007-05-01
Generation of clinical grade dendritic cells with capacity to produce biologically active IL-12p70.
2007-04-12
Natural and synthetic TLR7 ligands inhibit CpG-A- and CpG-C-oligodeoxynucleotide-induced IFN-alpha production.
2007-04-01
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Subjects applied up to 500 mg of study drug per day to up to 4 target lesions in the 0.06% group or to 5 target lesions in the 0.03% group covering a surface area of up to 100 cm^2. Dosing was started at 3 times per week, and patients were evaluated every 2 weeks. Dosing frequency (1, 2, 3, 5, or 7 times per week) was adjusted in a stepwise manner every 2 weeks based on physician assessment of tolerability (maintained, increased, decreased with or without a dosing interruption). Resiquimod was applied for 8 weeks followed by a 4-week no-treatment period to allow resiquimod-induced inflammation to resolve so that accurate skin scores could be obtained. Resiquimod has also been investigated as an oral treatment of HCV infection in a Phase IIa study in which patients received a 0.01 mg/kg dose of resiquimod twice weekly for 4 weeks.
Topical -- up to 500 mg of resiquimod as a gel (0.06% and 0.03%) covering a surface area of up to 100 cm^2. Oral -- 0.01 mg/kg dose of resiquimod twice weekly for 4 weeks.
Route of Administration: Other
THP-1 cells were exposed for 2, 4, 8 and 16 h with 0.1 mg/ml of resiquimod. Resiquimod induce decrease in hypoxia-inducible factor-1a (HIF-1a) prolyl hydroxylase (PHD) activity
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:13:55 GMT 2025
Edited
by admin
on Mon Mar 31 18:13:55 GMT 2025
Record UNII
V3DMU7PVXF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RESIQUIMOD
INN   MART.   MI   WHO-DD  
INN   USAN  
Official Name English
R848
Preferred Name English
CD11301
Code English
RESIQUIMOD [USAN]
Common Name English
1H-Imidazo[4,5-c]quinoline-1-ethanol, 4-amino-2-(ethoxymethyl)-?,?-dimethyl-
Systematic Name English
Resiquimod [WHO-DD]
Common Name English
4-Amino-2-(ethoxymethyl)-?,?-dimethyl-1H-imidazo[4,5-c]quinoline-1-ethanol
Systematic Name English
RESIQUIMOD [MART.]
Common Name English
S-28463
Code English
RESIQUIMOD [MI]
Common Name English
R-848
Code English
resiquimod [INN]
Common Name English
CD-11301
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 569016
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
EU-Orphan Drug EU/3/16/1653
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
NCI_THESAURUS C129820
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
Code System Code Type Description
DRUG BANK
DB06530
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
NCI_THESAURUS
C63958
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
CAS
144875-48-9
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
EPA CompTox
DTXSID7040603
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
INN
7937
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
MERCK INDEX
m9541
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
Resiquimod
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
ChEMBL
CHEMBL383322
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
CHEBI
36706
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
FDA UNII
V3DMU7PVXF
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
MESH
C402365
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
PUBCHEM
159603
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
USAN
KK-64
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
SMS_ID
100000177248
Created by admin on Mon Mar 31 18:13:55 GMT 2025 , Edited by admin on Mon Mar 31 18:13:55 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
TARGET ORGANISM->INHIBITOR
LABELED -> NON-LABELED
TARGET -> AGONIST
SALT/SOLVATE -> PARENT
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
ACTIVE MOIETY