Iodide

Iodide

SCHEMBL4294074

I.[Zn]CI

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG

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

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL954993 0.93
Iodide SCHEMBL8245354 0.68
SCHEMBL955305 0.67
Iodide SCHEMBL299359 0.57
SCHEMBL1331208 0.57
SCHEMBL185 0.57
Iodide SCHEMBL6852940 0.57
SCHEMBL716666 0.51
SCHEMBL1241351 0.51
Phosphine SCHEMBL6243734 0.51

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200385374-A1 IMIDAZOLE-BASED ANTICANCER AGENTS AND DERIVATIVES THEREOF, AND METHODS OF MAKING AND USING SAME THE UNIVERSITY OF TOLEDO (US) 2020-12-10 US claimed
WO-2019036607-A1 IMIDAZOLE-BASED ANTICANCER AGENTS AND DERIVATIVES THEREOF, AND METHODS OF MAKING AND USING SAME THE UNIVERSITY OF TOLEDO (US) 2019-02-21 WO claimed
US-20260001903-A1 ASCAROSIDE DERIVATIVES AND METHODS OF USE CALIFORNIA INSTITUTE OF TECHNOLOGY 2026-01-01 US disclosed
US-20250367232-A1 HALOGEN TREATMENT OF HEART ATTACK AND ISCHEMIC INJURY HUTCHINSON FRED CANCER RES (US) 2025-12-04 US disclosed
US-12473323-B2 Ascaroside derivatives and methods of use CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2025-11-18 US disclosed
US-20250282621-A1 CARBON NANOTUBE COMPOSITE COMPRISING MECHANICAL L IGANDS NANOCORE APS (DK) 2025-09-11 US disclosed
US-20250188206-A1 BIO-BASED ETHYLENE FOR THE PRODUCTION OF BIO-BASED POLYMERS, COPOLYMERS, AND OTHER BIO-BASED CHEMICAL COMPOUNDS XYLECO, INC. 2025-06-12 US disclosed
CN-119059879-A Cyclopropanation of substituted olefins 国际香料和香精公司 2024-12-03 CN disclosed
CN-114423774-B Ascaroside derivatives and methods of use 加利福尼亚技术学院 2024-11-08 CN disclosed
CN-118382616-A Synthesis method of complement factor D inhibitor and intermediate thereof 阿雷克森制药公司 2024-07-23 CN disclosed
US-12016880-B2 Halogen treatment of heart attack and ischemic injury FRED HUTCHINSON CANCER CENTER (US) 2024-06-25 US disclosed
US-4977265-A WITH BACTERICIDAL ACTIVITY HOFFMANN-LA ROCHE INC. (US) 1990-12-11 US disclosed
US-4946847-A BACTERICIDES HOFFMANN-LA ROCHE INC. (US) 1990-08-07 US disclosed
EP-0113561-B1 PROSTAGLANDIN INTERMEDIATES, THEIR SYNTHESIS AND THEIR CONVERSION TO PROSTAGLANDINS THE UPJOHN COMPANY (US) 1989-03-15 EP disclosed
US-4806541-A ANTIBACTERIAL AGENTS HOFFMANN-LA ROCHE INC. (US) 1989-02-21 US disclosed
US-4549030-A PROSTAGLANDIN DERIVATIVES THE UPJOHN COMPANY (US) 1985-10-22 US disclosed
US-4535173-A Intermediates for the production of prostaglandins from D-glucose THE UPJOHN COMPANY (US) 1985-08-13 US disclosed
EP-0113561-A2 Prostaglandin intermediates, their synthesis and their conversion to prostaglandins THE UPJOHN COMPANY (US) 1984-07-18 EP disclosed
US-4242332-A 4,5-Methano-bufadienolide-rhamnosides, their preparation, and drugs containing these compounds BASF AKTIENGESELLSCHAFT (DE) 1980-12-30 US disclosed
US-4022808-A ZINC-ALUMINUM-TITANIUM-TIN-IRON OR GROUP 5A AS CATALYSTS NIPPON SODA COMPANY LIMITED (JA) 1977-05-10 US disclosed