Iodide

Iodide

SCHEMBL5086967

[I-].c1ccc(C[P+](Cc2ccccc2)(Cc2ccccc2)Cc2ccccc2)cc1

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 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.50
CALM1 P0DP23 1/20 0.47
TAAR1 Q96RJ0 4/20 0.46
SLC6A2 P23975 2/20 0.46
SIGMAR1 Q99720 2/20 0.46
MAOA P21397 1/20 0.46
SLC6A4 P31645 1/20 0.46
SLC6A3 Q01959 1/20 0.46
CYP2A6 P11509 1/20 0.46
ADORA2A P29274 1/20 0.46
ADORA1 P30542 1/20 0.46
CYP1A2 P05177 1/20 0.44
TSHR P16473 2/20 0.43
IDO1 P14902 1/20 0.43
TP53 P04637 1/20 0.43
LOXL2 Q9Y4K0 1/20 0.43
TRPA1 O75762 1/20 0.43
ALDH1A1 P00352 1/20 0.43
SLC18A2 Q05940 1/20 0.42
ANPEP P15144 1/20 0.42

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
Bromide SCHEMBL5091934 0.94 EPHX1 (0.50) EPHX1CALM1TAAR1SLC6A2SIGMAR1
Hydrochloric Acid SCHEMBL5091807 0.94 EPHX1 (0.50) EPHX1CALM1TAAR1SLC6A2SIGMAR1
Water SCHEMBL10936916 0.94 EPHX1 (0.50) EPHX1CALM1TAAR1SLC6A2SIGMAR1
SCHEMBL9496837 0.88 EPHX1 (0.46) EPHX1CALM1TAAR1SLC6A2SIGMAR1
SCHEMBL7178324 0.86 EPHX1 (0.44) EPHX1CALM1TAAR1SLC6A2SIGMAR1
Iodide SCHEMBL5086904 0.84 TP53 (0.48) EPHX1TAAR1SLC6A2SIGMAR1MAOA
Iodide SCHEMBL5086624 0.84 TP53 (0.48) EPHX1TAAR1SLC6A2SIGMAR1MAOA
Iodide SCHEMBL5091410 0.84 TP53 (0.48) EPHX1TAAR1SLC6A2SIGMAR1MAOA
SCHEMBL7170403 0.84 EPHX1 (0.42) EPHX1CALM1TAAR1SLC6A2SIGMAR1
SCHEMBL7178357 0.84 EPHX1 (0.42) EPHX1CALM1TAAR1SLC6A2SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
EP-0161550-B1 PROCESS FOR PRODUCING AN ALIPHATIC ISOCYANATE Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1988-01-20 EP disclosed
US-4587056-A CARBONYLATION, OXIDATION, CATALYST ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1986-05-06 US disclosed
EP-0161550-A1 Process for producing an aliphatic isocyanate Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1985-11-21 EP disclosed
US-4124630-A Process for the production of chloromethyl thiocyanate OFFERMANNS HERIBERT 1978-11-07 US disclosed
US-4052427-A PROCESS FOR THE PREPARATION OF DIALKYLTIN DIHALIDES WITCO CHEMICAL CORPORATION (US) 1977-10-04 US disclosed