Iodide

Iodide

SCHEMBL9166011

CCCCCCCCCCCCCCOc1ccc(CC(=O)Nc2ccc(-n3cc[n+](C)c3C)cc2)cc1.[I-]

nearest known ligand 0.50

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 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.47
CYP2D6 P10635 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
CYP2C19 P33261 1/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
GAA P10253 1/20 0.46
SMN1; SMN2 Q16637 3/20 0.46
KDM4E B2RXH2 1/20 0.46
CYP1A2 P05177 1/20 0.46
PDE4A P27815 1/20 0.46
HIF1A Q16665 1/20 0.46
HDAC10 Q969S8 1/20 0.46
HDAC6 Q9UBN7 1/20 0.46
LMNA P02545 1/20 0.44
NPC1 O15118 1/20 0.43
HPGD P15428 1/20 0.43
RAB9A P51151 1/20 0.43
FAAH O00519 4/20 0.43

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 SCHEMBL9169587 0.89 NLRP3 (0.46) MAPTCYP2D6MEN1KMT2ASMN1; SMN2
SCHEMBL9159435 0.82 CYP2D6 (0.62) MAPTCYP2D6CYP2C19L3MBTL1GAA
Hydrochloric Acid SCHEMBL9168856 0.81 CYP2D6 (0.61) MAPTCYP2D6CYP2C19L3MBTL1GAA
Iodide SCHEMBL9166019 0.79 SMN1; SMN2 (0.49) MAPTCYP2D6L3MBTL1GAASMN1; SMN2
SCHEMBL9166917 0.76 SMN1; SMN2 (0.59) MAPTCYP2D6L3MBTL1GAASMN1; SMN2
Hydrochloric Acid SCHEMBL9167319 0.75 MAPT (0.53) MAPTCYP2D6L3MBTL1GAASMN1; SMN2
Iodide SCHEMBL9166006 0.72 GAA (0.47) MAPTCYP2D6MEN1KMT2AL3MBTL1
Bromide SCHEMBL9169340 0.72 MAPT (0.55) MAPTCYP2D6L3MBTL1GAASMN1; SMN2
Bromide SCHEMBL9167422 0.72 MAPT (0.49) MAPTCYP2D6L3MBTL1GAASMN1; SMN2
Bromide SCHEMBL9166550 0.72 MAPT (0.49) MAPTCYP2D6L3MBTL1GAASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5432189-A Bis-aryl amide and urea antagonists of platelet activating factor AMERICAN CYANAMID COMPANY (US) 1995-07-11 US disclosed
US-5350759-A Bis-aryl urea compounds WISSNER ALLAN (US) 1994-09-27 US disclosed
US-5231182-A Platelet activating factor inhibitor AMERICAN CYANAMID COMPANY (US) 1993-07-27 US disclosed
EP-0458037-A1 Bis-aryl amide and urea antagonists of platelet activating factor AMERICAN CYANAMID COMPANY (US) 1991-11-27 EP disclosed