Iodide

Iodide

SCHEMBL5088044

CCCC[N+](CC)(CC)CC.[I-]

nearest known ligand 0.72

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 17)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 5/20 0.72
SLC22A1 O15245 3/20 0.69
SLC22A2 O15244 1/20 0.59
TSHR P16473 2/20 0.53
ALDH1A1 P00352 1/20 0.53
TP53 P04637 1/20 0.53
CYP3A4 P08684 1/20 0.53
ALOX15 P16050 1/20 0.53
ALOX12 P18054 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
HIF1A Q16665 1/20 0.53
HSD17B10 Q99714 1/20 0.53
NFKB1 P19838 1/20 0.44
KCNA1 Q09470 1/20 0.44
KDM4E B2RXH2 1/20 0.41
PMP22 Q01453 1/20 0.41
ATM Q13315 1/20 0.41

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
SCHEMBL1239368 0.97 DNM1 (0.77) DNM1SLC22A1SLC22A2TSHRALDH1A1
Bromide SCHEMBL10701064 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Bromide SCHEMBL622840 0.93 DNM1 (0.78) DNM1SLC22A1SLC22A2TSHRALDH1A1
SCHEMBL17800111 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Iodide SCHEMBL5086874 0.93 SLC22A1 (0.69) DNM1SLC22A1SLC22A2TSHRALDH1A1
Iodide SCHEMBL4333792 0.93 SLC22A1 (0.69) DNM1SLC22A1SLC22A2TSHRALDH1A1
Water SCHEMBL999491 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Hydrochloric Acid SCHEMBL394062 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Fluoride Ion SCHEMBL31559159 0.93 DNM1 (0.72) DNM1SLC22A1SLC22A2TSHRALDH1A1
Tetrabuthylammonium SCHEMBL6242211 0.90 SLC22A1 (0.75) DNM1SLC22A1SLC22A2TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112608258-A Method for synthesizing 4,4' -dichlorodiphenyl sulfone by sulfoxide oxidation method 江苏傲伦达科技实业股份有限公司 2021-04-06 CN claimed
CN-101402599-A Bi(2,2,6,6-tetramethyl piperidine nitrogen oxygen free radical) ether ester and method of preparing the same HUAIHAI INST TECHNOLOGY (CN) 2009-04-08 CN claimed
CN-118239957-A Process for the preparation of 2-exo- (2-methylbenzyloxy) -1-methyl-4-isopropyl-7-oxabicyclo [2.2.1] heptane 巴斯夫农业公司 2024-06-25 CN disclosed
CN-110337438-B Process for the preparation of 2-exo- (2-methylbenzyloxy) -1-methyl-4-isopropyl-7-oxabicyclo [2.2.1] heptane 巴斯夫农业公司 2024-03-26 CN disclosed
CN-112608258-A Method for synthesizing 4,4' -dichlorodiphenyl sulfone by sulfoxide oxidation method 江苏傲伦达科技实业股份有限公司 2021-04-06 CN disclosed
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
CN-1114834-A antidiabetic agent OTSUKA PHARMA CO LTD (JP) 1996-01-10 CN disclosed
EP-0670831-A1 QUINOXALINE DERIVATIVE AS ANTIDIABETIC AGENT OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1995-09-13 EP disclosed
WO-1995009159-A1 QUINOXALINE DERIVATIVE AS ANTIDIABETIC AGENT OTSUKA PHARMACEUTICAL COMPANY, LIMITED (JP) 1995-04-06 WO disclosed
US-4150057-A ION EXCHANGING, REACTION OF BORON COMPOUND WITH DIMETHYL SULFIDE AND HYDROCHLORIC ACID THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1979-04-17 US disclosed