Iodide

Iodide

SCHEMBL7209608

I.[CaH2].[CaH2]

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
Iodide SCHEMBL18708 1.00
SCHEMBL27948499 1.00
Iodide SCHEMBL11424244 1.00
Iodide SCHEMBL9791887 0.82
Iodide SCHEMBL8901438 0.82
Bromide SCHEMBL11505479 0.82
Iodide SCHEMBL28519642 0.82
Iodide SCHEMBL4416035 0.82
Iodide SCHEMBL9064090 0.82
Iodide SCHEMBL4204495 0.82

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6624143-B1 Antibiotics of the amphomycin type are characterized by the exocyclic amino acid aspartic acid (Asp, cyclic oligopeptides Antimicrobial Agents and Chemotherapy AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2003-09-23 US disclosed