Iodide

Iodide

SCHEMBL2899228

[I-].c1ccc([N+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.56

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 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.33
APOBEC3A P31941 1/20 0.56
APOBEC3G Q9HC16 1/20 0.56
ALDH1A1 P00352 5/20 0.38
TSHR P16473 4/20 0.33
TDP1 Q9NUW8 4/20 0.33
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA9 Q16790 2/20 0.33
LMNA P02545 2/20 0.33
CA12 O43570 1/20 0.33
GLA P06280 1/20 0.33
CA3 P07451 1/20 0.33
CA4 P22748 1/20 0.33
CA14 Q9ULX7 1/20 0.33
ALOX12 P18054 1/20 0.33
CES2 O00748 1/20 0.33
CES1 P23141 1/20 0.33
CA7 P43166 1/20 0.33
HSD17B10 Q99714 2/20 0.32

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
SCHEMBL414301 0.96 APOBEC3A (0.50) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Water SCHEMBL187879 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Fluoride Ion SCHEMBL2481380 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Methane SCHEMBL27907628 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Hydrochloric Acid SCHEMBL123613 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
SCHEMBL12762124 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Bromide SCHEMBL130138 0.92 APOBEC3A (0.47) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Bromide SCHEMBL8580336 0.89 APOBEC3A (0.45) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1
Iodide SCHEMBL11359680 0.87 APOBEC3A (0.52) APOBEC3AAPOBEC3GTSHRTDP1LMNA
SCHEMBL6238199 0.86 APOBEC3A (0.43) APOBEC3AAPOBEC3GALDH1A1TSHRTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7842127-B2 Corrosion inhibitor composition comprising a built-in intensifier NALCO COMPANY (US) 2010-11-30 US claimed
WO-2008077005-A1 CORROSION INHIBITOR COMPOSITION COMPRISING A BUILT-IN INTENSIFIER NALCO COMPANY (US) 2008-06-26 WO claimed
US-20080146464-A1 CORROSION INHIBITOR COMPOSITION COMPRISING A BUILT-IN INTENSIFIER APERGY BMCS ACQUISITION CORP 2008-06-19 US claimed
EP-1144990-A1 A REFERENCE ELECTRODE SOLUTION CONTAINING ORGANIC AMMONIUM AND PHOSPHONIUM SALTS FOR POTENTIOMETRIC MEASUREMENT OF pH BAXTER INTERNATIONAL INC. (US) 2001-10-17 EP claimed
WO-2000033064-A9 A REFERENCE ELECTRODE SOLUTION CONTAINING ORGANIC AMMONIUM AND PHOSPHONIUM SALTS FOR POTENTIOMETRIC MEASUREMENT OF pH BAXTER INT (US) 2001-03-29 WO claimed
WO-2000033064-A1 A REFERENCE ELECTRODE SOLUTION CONTAINING ORGANIC AMMONIUM AND PHOSPHONIUM SALTS FOR POTENTIOMETRIC MEASUREMENT OF pH BAXTER INTERNATIONAL INC. (US) 2000-06-08 WO claimed
US-5066373-A Hydrogen electrode, double junction reference electrode with quaternary ammonium salt in outer shell ALLIED-SIGNAL INC. (US) 1991-11-19 US claimed
US-12515973-B1 Scale treatment in geothermal or extremely high temperature wells HALLIBURTON ENERGY SERVICES, INC. (US) 2026-01-06 US disclosed
US-12247166-B2 Drag reducing agent for emulsified acids HALLIBURTON ENERGY SERVICES, INC. (US) 2025-03-11 US disclosed
US-20240384161-A1 Drag Reducing Agent for Emulsified Acids HALLIBURTON ENERGY SERVICES, INC. (US) 2024-11-21 US disclosed
WO-2024237937-A1 FLUID FLOW ENHANCEMENT OF ACID EMULSION HALLIBURTON ENERGY SERVICES, INC. (US) 2024-11-21 WO disclosed
US-11946841-B2 Control of industrial water treatment via digital imaging ECOLAB USA INC. (US) 2024-04-02 US disclosed
EP-4166712-A1 METHOD FOR PRODUCING COAGULATED MATERIAL DIC Corporation (JP) 2023-04-19 EP disclosed
US-4429165-A TRIVALENT ORGANOPHOSPHORUS AND ORGANONITROGEN COMPOUNDS AS PROMOTERS UNION CARBIDE CORPORATION (US) 1984-01-31 US disclosed
EP-0034374-B1 SELECTIVE HOMOLOGATION OF ACETALS OR ETHERS TO MONOHYDRIC OR POLYHYDRIC ALCOHOLS UNION CARBIDE CORPORATION (US) 1983-08-03 EP disclosed
US-4337365-A COBALT AND IODIDE CATALYST, HIGH TEMPERATURE, INERT ETHER SOLVENT UNION CARBIDE CORPORATION (US) 1982-06-29 US disclosed
EP-0037580-A1 Process for the selective homologation of methanol to ethanol UNION CARBIDE CORPORATION (US) 1981-10-14 EP disclosed
EP-0034374-A1 Selective homologation of acetals or ethers to monohydric or polyhydric alcohols UNION CARBIDE CORPORATION (US) 1981-08-26 EP disclosed
US-4277634-A SYNERGISTIC COMBINATION OF COBALT CATALYST, IODINE PROMOTER, AND INERT SOLVENT UNION CARBIDE CORPORATION (US) 1981-07-07 US disclosed
US-4124630-A Process for the production of chloromethyl thiocyanate OFFERMANNS HERIBERT 1978-11-07 US disclosed