Iodide

Iodide

SCHEMBL5087203

CCCCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC.[I-]

nearest known ligand 0.94

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.

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 7/20 0.94
TSHR P16473 2/20 0.50
THRB P10828 1/20 0.50
LMNA P02545 1/20 0.42
BDKRB2 P30411 3/20 0.41
CA2 P00918 1/20 0.39
OPRM1 P35372 1/20 0.39
ALDH1A1 P00352 1/20 0.38

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
Iodide SCHEMBL5091656 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5088416 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5085198 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL3858577 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5091864 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5087043 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5086658 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5088125 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5085433 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5091621 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 US claimed
US-4574158-A Acetal purification using phase transfer catalysts CONOCO INC. (US) 1986-03-04 US claimed
US-4513144-A Acetal purification with superoxides CONOCO INC. (US) 1985-04-23 US claimed
US-4451680-A RUTHENIUM COMPOUND, BIDENTATE OR MULTIDENTATE PHOSPHINE, PHOSPHONIUM COMPOUND TEXACO INC. (US) 1984-05-29 US claimed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 US claimed
JP-60001155-A None JP disclosed
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 US disclosed
US-11981844-B2 Composition, film, laminated structure, light-emitting device and display SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2024-05-14 US disclosed
CN-112912464-B Composition, film, laminated structure, light-emitting device, and display 住友化学株式会社 2023-12-29 CN disclosed
CN-112930383-B Composition, film, laminated structure, light-emitting device, and display 住友化学株式会社 2023-09-08 CN disclosed
CN-111670240-B Composition, film, laminate structure, light emitting device, and display 住友化学株式会社 2023-06-09 CN disclosed
CN-111655818-B Composition, film, laminate structure, light emitting device, and display 住友化学株式会社 2023-05-09 CN disclosed
US-4371646-A 2,6-Di-tertiary butyl phenyl phosphites and synthetic resin compositions having enhanced stability to heat and light ADEKA ARGUS CHEMICAL CO. LTD. (JP) 1983-02-01 US disclosed
EP-0001825-B1 METHOD OF PREPARING 2,4-DIFLUOROANILINE MERCK & CO. INC. (US) 1982-01-13 EP disclosed
EP-0025846-A1 Improved process for the preparation of vinylcyclopropane derivatives NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1981-04-01 EP disclosed
US-4252739-A ALKYLATING AGENT SUCH AS 1,4-DIHALO-2-BUTENE, AN ACTIVE METHYLENE COMPOUND, A CATALYTIC ONIUM COMPOUND, AN ALKALI METAL COMPOUND AND WATER; ONE STEP EMERY INDUSTRIES, INC. (US) 1981-02-24 US disclosed
US-4160116-A FROM THE CORRESPONDING OXIDE BY HYDRATION USING ORGANIC PHOSPHONIUM HALIDE CATALYST, CARBON DIOXIDE SHOWA DENKO K.K. (JP) 1979-07-03 US disclosed
EP-0001825-A1 Method of preparing 2,4-difluoroaniline MERCK & CO. INC. (US) 1979-05-16 EP disclosed
US-4140719-A Solid-liquid phase transfer catalysis improved method of preparing 2,4-difluoroaniline MERCK & CO., INC. (US) 1979-02-20 US disclosed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 US disclosed