Iodide

Iodide

SCHEMBL6060968

Cc1ccccc1[P+](Cc1ccccc1)(c1ccccc1C)c1ccccc1C.[I-]

nearest known ligand 0.41

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 0.36
TAAR1 Q96RJ0 4/20 0.39
SLC6A2 P23975 2/20 0.39
SIGMAR1 Q99720 2/20 0.39
MAOA P21397 1/20 0.39
SLC6A4 P31645 1/20 0.39
SLC6A3 Q01959 1/20 0.39
CYP2A6 P11509 1/20 0.39
ADORA2A P29274 1/20 0.39
ADORA1 P30542 1/20 0.39
SCN4A P35499 2/20 0.39
EPHX1 P07099 1/20 0.37
SLC18A2 Q05940 1/20 0.36
CYP2D6 P10635 1/20 0.36
SNCA P37840 2/20 0.36
TSHR P16473 1/20 0.36
TP53 P04637 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
TRPA1 O75762 1/20 0.35
ALDH1A1 P00352 1/20 0.35

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
Hydrochloric Acid SCHEMBL6060719 0.96 TAAR1 (0.39) TAAR1SLC6A2SIGMAR1MAOASLC6A4
Bromide SCHEMBL6060755 0.96 SNCA (0.39) TAAR1SLC6A2SIGMAR1MAOASLC6A4
Iodide SCHEMBL7197262 0.88 IDO1 (0.35) TAAR1CYP2A6SNCATSHRACHE
Phosphoric Acid SCHEMBL7195799 0.87 LAP3 (0.40) TSHRL3MBTL1ALDH1A1LMNANPSR1
Hydrochloric Acid SCHEMBL11410207 0.86 SNCA (0.44) TAAR1SLC6A2SIGMAR1MAOASLC6A4
Bromide SCHEMBL8053180 0.86 SNCA (0.47) TAAR1SLC6A2SIGMAR1MAOASLC6A4
Hydrochloric Acid SCHEMBL9850761 0.86 SNCA (0.44) TAAR1SLC6A2SIGMAR1MAOASLC6A4
Acetic Acid SCHEMBL8750049 0.86 POLB (0.44) TSHRL3MBTL1ALDH1A1LMNA
Acetic Acid SCHEMBL7197002 0.84 POLB (0.42) TSHRL3MBTL1ALDH1A1LMNA
Bromide SCHEMBL7197753 0.84 SNCA (0.37) TAAR1CYP2A6SNCATSHRACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1993004122-A1 POLYESTER COMPOSITIONS CONTAINING PHOSPHONIUM COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO claimed
US-20060229400-A1 Powder coating matting agent comprising ester amide condensation product FLETCHER TIM 2006-10-12 US disclosed
US-20050288450-A1 Coating matting agent comprising amide condensation product FLETCHER TIM 2005-12-29 US disclosed
EP-1509561-A1 POWDER COATING MATTING AGENT COMPRISING ESTER AMIDE CONDENSATION PRODUCT Grace GmbH & Co. KG (DE) 2005-03-02 EP disclosed
WO-2003102048-A1 POWDER COATING MATTING AGENT COMPRISING ESTER AMIDE CONDENSATION PRODUCT GRACE GMBH & CO. KG (DE) 2003-12-11 WO disclosed
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed
WO-1993004122-A1 POLYESTER COMPOSITIONS CONTAINING PHOSPHONIUM COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO disclosed