Iodide

Iodide

SCHEMBL8748435

Cc1cc(C)[n+](C)c(C)c1.[I-]

nearest known ligand 0.35

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 10)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.32
ALDH1A1 P00352 2/20 0.35
TSHR P16473 1/20 0.35
KDM4E B2RXH2 1/20 0.33
HTT P42858 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
SELL P14151 1/20 0.32
SELP P16109 1/20 0.32
SELE P16581 1/20 0.32
RAPGEF4 Q8WZA2 1/20 0.30

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
SCHEMBL2601901 0.97 ALDH1A1 (0.37) ALDH1A1TSHRKDM4EHTTSMN1; SMN2
Water SCHEMBL3791699 0.93 ALDH1A1 (0.35) ALDH1A1TSHRKDM4EHTTSMN1; SMN2
Bromide SCHEMBL11433606 0.93 ALDH1A1 (0.35) ALDH1A1TSHRKDM4EHTTSMN1; SMN2
Hydrochloric Acid SCHEMBL7252277 0.93 KDM4E (0.38) ALDH1A1TSHRKDM4EHTTSMN1; SMN2
SCHEMBL5159873 0.76 KDM4E (0.50) ALDH1A1TSHRKDM4EHTTSMN1; SMN2
SCHEMBL10679825 0.72 IDO1 (0.31)
SCHEMBL18230630 0.71 GAA (0.45) ALDH1A1SMN1; SMN2RAPGEF4
SCHEMBL25447157 0.67 KDM4E (0.39) ALDH1A1KDM4EHTTSMN1; SMN2ACHE
Iodide SCHEMBL31265537 0.67 MAPT (0.44) ALDH1A1KDM4EHTTSMN1; SMN2
SCHEMBL138421 0.67 ALDH1A1 (0.35) ALDH1A1TSHRSELLSELPSELE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5494572-A SOLVENT EXTRACTION WITH PYRIDINIUM SALT GENERAL SEKIYU KABUSHIKIKAISHA (JP) 1996-02-27 US claimed
CN-107580613-B Fluoroelastomer composition 索尔维特殊聚合物意大利有限公司 2020-11-13 CN disclosed
CN-106147754-B Polystyrene substituted pyridine compound as G-quadruplex nucleic acid fluorescent probe 广东工业大学 2020-03-06 CN disclosed
US-20180142050-A1 FLUOROELASTOMER COMPOSITION SOLVAY SPECIALTY POLYMERS ITALY S.P.A. (IT) 2018-05-24 US disclosed
EP-3294801-A1 FLUOROELASTOMER COMPOSITION Solvay Specialty Polymers Italy S.p.A. (IT) 2018-03-21 EP disclosed
WO-2016180660-A1 FLUOROELASTOMER COMPOSITION SOLVAY SPECIALTY POLYMERS ITALY S.P.A. (IT) 2016-11-17 WO disclosed
EP-0653477-B1 Use of an organic solvent for denitrogenationation of light oil by extraction GEN SEKIYU KABUSHIKI KAISHA (JP) 1997-03-12 EP disclosed
EP-0538738-B1 Desulfurization and Decolourizing of light oil by extraction GEN SEKIYU KABUSHIKI KAISHA (JP) 1996-07-10 EP disclosed
US-5494572-A SOLVENT EXTRACTION WITH PYRIDINIUM SALT GENERAL SEKIYU KABUSHIKIKAISHA (JP) 1996-02-27 US disclosed
EP-0653477-A2 Desulfurization and denitration of light oil by extraction GENERAL SEKIYU KABUSHIKI KAISHA (JP) 1995-05-17 EP disclosed
EP-0538738-A2 Desulfurization and Decolourizing of light oil by extraction GENERAL SEKIYU KABUSHIKI KAISHA (JP) 1993-04-28 EP disclosed