Imiquimod

Imiquimod

SCHEMBL1301796

CC(C)Cn1cnc2c(N)nc3ccccc3c21.Cl

nearest known ligand 0.97

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 0.97
PDE4D Q08499 2/20 0.97
ADORA2A P29274 2/20 0.97
LMNA P02545 1/20 0.97
POLB P06746 1/20 0.97
HRH2 P25021 1/20 0.97
ADRA1D P25100 1/20 0.97
HTR2A P28223 1/20 0.97
ADRA1A P35348 1/20 0.97
NUDT1 P36639 1/20 0.97
HTR2B P41595 1/20 0.97
KCNH2 Q12809 1/20 0.97
TLR8 Q9NR97 7/20 0.51
PDE4A P27815 1/20 0.46
PDE4B Q07343 1/20 0.46
PDE4C Q08493 1/20 0.46
TEK Q02763 1/20 0.43
CYP2D6 P10635 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41

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 SCHEMBL26136 0.99 TLR7 (1.00) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL29357252 0.99 TLR7 (1.00) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL570774 0.99 TLR7 (1.00) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL29029396 0.97 TLR7 (0.93) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL17962753 0.97 TLR7 (0.97) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL5262205 0.93 TLR7 (0.88) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL3191041 0.92 TLR7 (0.86) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL3415170 0.91 TLR7 (0.84) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL5260618 0.90 TLR7 (0.82) TLR7PDE4DADORA2ALMNAPOLB
Imiquimod SCHEMBL9602834 0.90 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

Claimed or disclosed in 78 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112438944-B Temperature-sensitive gel pharmaceutical composition for treating tumors 苏州百迈生物医药有限公司 2024-07-02 CN claimed
CN-116212016-A Immune adjuvant-loaded phycocyanin nano-system and preparation method and application thereof 江苏大学 2023-06-06 CN claimed
WO-2021042778-A1 TEMPERATURE-SENSITIVE GEL PHARMACEUTICAL COMPOSITION FOR TREATMENT OF TUMORS 苏州百迈生物医药有限公司 2021-03-11 WO claimed
CN-112438944-A Temperature-sensitive gel pharmaceutical composition for treating tumors 苏州百迈生物医药有限公司 2021-03-05 CN claimed
CN-111375065-A Biopolymer pharmaceutical composition for tumor treatment 苏州百迈生物医药有限公司 2020-07-07 CN claimed
CN-111375062-A Biopolymer pharmaceutical composition for in-situ gel-forming chemotherapy and immune combination therapy 苏州百迈生物医药有限公司 2020-07-07 CN claimed
CN-110693850-A Preparation method of imiquimod chitosan nanoparticles 湖北科益药业股份有限公司 2020-01-17 CN claimed
CN-104402878-A Preparation method of imiquimod TIANFANG PHARMACEUTICAL CO LTD 2015-03-11 CN claimed
EP-0394026-B1 Formulation containing an imidazo[4,5-c]quinolin derivative RIKER LABORATORIES, INC. (US) 1993-09-29 EP claimed
WO-2025104289-A1 ANTINEOPLASTIC COMBINATIONS MEDINCELL S.A. (FR) 2025-05-22 WO disclosed
CN-113730570-B Chemotherapy immune combination medicine and application thereof 苏州百迈生物医药有限公司 2025-05-09 CN disclosed
US-20240398841-A1 BLADDER PERFUSION PHARMACEUTICAL COMPOSITION, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF INNOBM PHARMACEUTICALS CO., LTD. (CN) 2024-12-05 US disclosed
CN-118845625-A Imiquimod hydrogel and application thereof in preparation of HPV immunotherapy medicaments 浙江大学 2024-10-29 CN disclosed
CN-114681612-B Bladder perfusion medicine and preparation method and application thereof 苏州百迈生物医药有限公司 2024-10-25 CN disclosed
EP-0310950-B1 Quinoline intermediates for the synthesis of 1H-imidazo[4,5-c]quinolines and 1H-imidazo[4,5-c]quinolin-4-amimes RIKER LABORATORIES, INC. (US) 1993-01-13 EP disclosed
EP-0394026-A1 Formulation containing an imidazo[4,5-c]quinolin derivative RIKER LABORATORIES, INC. (US) 1990-10-24 EP disclosed
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 disclosed
EP-0310950-A1 Quinoline intermediates for the synthesis of 1H-imidazo[4,5-c]quinolines and 1H-imidazo[4,5-c]quinolin-4-amimes RIKER LABORATORIES, INC. (US) 1989-04-12 EP disclosed
US-4689338-A 1H-Imidazo[4,5-c]quinolin-4-amines and antiviral use RIKER LABORATORIES, INC. (US) 1987-08-25 US disclosed
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 disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20240398841-A1 BLADDER PERFUSION PHARMACEUTICAL COMPOSITION, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF BAD, BPHL, HASPIN TLR7 728/4885PDE4D 1014/4885ADORA2A 1174/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.