Iodide

Iodide

SCHEMBL698825

[I-].[I-].[Tm+2]

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
SCHEMBL28005566 0.71
SCHEMBL59425 0.71
SCHEMBL28227086 0.71
Water SCHEMBL16776762 0.71
SCHEMBL30931513 0.71
Iodide SCHEMBL8080327 0.50 CA4 (0.33)
Iodide SCHEMBL6027905 0.50
Iodide SCHEMBL19755 0.50
Iodide SCHEMBL284808 0.50
Iodide SCHEMBL335403 0.50

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6887824-B1 Divalent lanthanide reduction catalysts THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-05-03 US claimed
EP-1242468-A1 DIVALENT LANTHANIDE REDUCTION CATALYSTS The Regents of the University of California (US) 2002-09-25 EP claimed
WO-2001021667-A1 DIVALENT LANTHANIDE REDUCTION CATALYSTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2001-03-29 WO claimed
CN-117551004-A Synthesis method of amino acid and amino alcohol compound 四川大学 2024-02-13 CN disclosed
EP-2443163-B1 POLYMERIZATION OF ISOPRENE FROM RENEWABLE RESOURCES DANISCO US INC (US) 2018-12-26 EP disclosed
US-9550839-B2 Copolymers of conjugated triene monomers for improved filler interaction THE GOODYEAR TIRE & RUBBER COMPANY (US) 2017-01-24 US disclosed
US-9296850-B2 Polymers of isoprene from renewable resources THE GOODYEAR TIRE & RUBBER COMPANY (US) 2016-03-29 US disclosed
US-20150376343-A1 COPOLYMERS OF CONJUGATED TRIENE MONOMERS FOR IMPROVED FILLER INTERACTION THE GOODYEAR TIRE & RUBBER COMPANY (US) 2015-12-31 US disclosed
US-20150203620-A1 POLYMERS OF ISROPENE FROM RENEWABLE RESOURCES DANISCO US INC. (US) 2015-07-23 US disclosed
US-9079980-B2 Copolymers of conjugated triene monomers for improved filler interaction THE GOODYEAR TIRE & RUBBER COMPANY (US) 2015-07-14 US disclosed
US-8940849-B2 Polymers of isropene from renewable resources THE GOODYEAR TIRE & RUBBER COMPANY (US) 2015-01-27 US disclosed
EP-2423239-A1 Copolymers of conjugated triene for improved filler interactions The Goodyear Tire & Rubber Company (US) 2012-02-29 EP disclosed
US-20110237769-A1 Polymers of isoprene from renewable resources THE GOODYEAR TIRE & RUBBER COMPANY (US) 2011-09-29 US disclosed
EP-2307552-A1 POLYMERS OF ISOPRENE FROM RENEWABLE RESOURCES The Goodyear Tire & Rubber Company (US) 2011-04-13 EP disclosed
US-20110040058-A1 POLYMERIZATION OF ISOPRENE FROM RENEWABLE RESOURCES THE GOODYEAR TIRE & RUBBER COMPANY 2011-02-17 US disclosed
WO-2010148144-A1 POLYMERIZATION OF ISOPRENE FROM RENEWABLE RESOURCES DANISCO US INC. (US) 2010-12-23 WO disclosed
WO-2010005525-A1 POLYMERS OF ISOPRENE FROM RENEWABLE RESOURCES THE GOODYEAR TIRE & RUBBER COMPANY (US) 2010-01-14 WO disclosed
US-6887824-B1 Divalent lanthanide reduction catalysts THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-05-03 US disclosed
EP-1242468-A1 DIVALENT LANTHANIDE REDUCTION CATALYSTS The Regents of the University of California (US) 2002-09-25 EP disclosed
WO-2001021667-A1 DIVALENT LANTHANIDE REDUCTION CATALYSTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2001-03-29 WO disclosed