Imiquimod

Imiquimod

SCHEMBL26136

CC(C)Cn1cnc2c(N)nc3ccccc3c21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TLR7

The experimentally established mechanism targets of Imiquimod. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TLR7 known ✓ Q9NYK1 15/20 1.00
PDE4D Q08499 2/20 1.00
ADORA2A P29274 2/20 1.00
LMNA P02545 1/20 1.00
POLB P06746 1/20 1.00
HRH2 P25021 1/20 1.00
ADRA1D P25100 1/20 1.00
HTR2A P28223 1/20 1.00
ADRA1A P35348 1/20 1.00
NUDT1 P36639 1/20 1.00
HTR2B P41595 1/20 1.00
KCNH2 Q12809 1/20 1.00
TLR8 Q9NR97 7/20 0.52
PDE4A P27815 1/20 0.47
PDE4B Q07343 1/20 0.47
PDE4C Q08493 1/20 0.47
TEK Q02763 1/20 0.44
CYP2D6 P10635 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Imiquimod SCHEMBL570774 1.00 TLR7 (1.00) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL29357252 1.00 TLR7 (1.00) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL17962753 0.99 TLR7 (0.97) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL1301796 0.99 TLR7 (0.97) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL29029396 0.96 TLR7 (0.93) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL5262205 0.94 TLR7 (0.88) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL3191041 0.93 TLR7 (0.86) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL3415170 0.92 TLR7 (0.84) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL5260618 0.91 TLR7 (0.82) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL9602834 0.91 TLR7 (0.82) TLR7PDE4DADORA2ALMNAPOLB

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 62191 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3993771-B1 SONODYNAMIC THERAPY INNOVATION ULSTER LTD (GB) 2026-05-27 EP claimed
US-20260139860-A1 PRODUCTS OF MANUFACTURE FOR THE TREATMENT, PREVENTION AND AMELIORATION OF MICROBIAL INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2026-05-21 US claimed
EP-4094767-B1 NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO UNIV EMORY (US) 2026-05-20 EP claimed
CN-122031668-A Formulations for neoplasia vaccines 博德研究所 2026-05-15 CN claimed
CN-122031401-A MOF-based drug delivery agent for multi-mechanism synergistic tumor treatment and preparation method thereof 理工清科(重庆)先进材料研究院有限公司 2026-05-15 CN claimed
US-20260132141-A1 PROTEIN PHOSPHATASE 2A ACTIVATORS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2026-05-14 US claimed
US-12622922-B2 Compositions and methods for metal containing formulations capable of modulating immune response THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2026-05-12 US claimed
US-12622956-B2 Methods and vaccines for inducing immune responses to multiple different MHC molecules Mayo Foundation for Medical Education and Research; (MN) 2026-05-12 US claimed
CN-122005785-A Method for identifying HIV patients susceptible to therapy with GP 120V 3 glycan-directed antibodies 吉利德科学公司 2026-05-12 CN claimed
US-20260116950-A1 NOVEL PEPTIDES AND COMBINATION OF PEPTIDES AND SCAFFOLDS THEREOF FOR USE IN IMMUNOTHERAPY AGAINST COLORECTAL CARCINOMA (CRC) AND OTHER CANCERS IMMATICS BIOTECHNOLOGIES GMBH (DE) 2026-04-30 US claimed
US-5238944-A Viricides comprising isotearic acid; skin disorders RIKER LABORATORIES, INC. (US) 1993-08-24 US claimed
EP-0553202-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[4,5-C]QUINOLIN-4-AMINES. MINNESOTA MINING & MFG (US) 1993-08-04 EP claimed
US-5175296-A Reacting 1H-imidazolo(4,5-c)quinolin-5N-oxide with organic isocyanate; hydrolysis MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-12-29 US claimed
WO-1992015581-A1 PROCESS FOR IMIDAZO[4,5-c]QUINOLIN-4-AMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-09-17 WO claimed
WO-1992006093-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[4,5-C]QUINOLIN-4-AMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-04-16 WO claimed
EP-0394026-A1 Formulation containing an imidazo[4,5-c]quinolin derivative RIKER LABORATORIES, INC. (US) 1990-10-24 EP claimed
EP-0376534-A1 Topical formulations and transdermal delivery systems containing 1-isobutyl-1H-imidazo[4,5-c]quinoline-4-amine RIKER LABORATORIES, INC. (US) 1990-07-04 EP claimed
EP-0145340-B1 1H-Imidazo[4,5-c]quinolines and 1H-imidazo[4,5-c]quinolin-4-amines RIKER LABORATORIES, INC. (US) 1990-01-24 EP claimed
US-4689338-A 1H-Imidazo[4,5-c]quinolin-4-amines and antiviral use RIKER LABORATORIES, INC. (US) 1987-08-25 US claimed
EP-0145340-A2 1H-Imidazo[4,5-c]quinolines and 1H-imidazo[4,5-c]quinolin-4-amines RIKER LABORATORIES, INC. (US) 1985-06-19 EP claimed