Iodide

Iodide

SCHEMBL3513621

[I-].c1ccc([P+](CC2CCOC2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.38

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
HIF1A Q16665 1/20 0.38
KDM1A O60341 1/20 0.34
MAOA P21397 1/20 0.34
MAOB P27338 1/20 0.34
KCNH3 Q9ULD8 1/20 0.33
NAMPT P43490 4/20 0.33
MCHR1 Q99705 1/20 0.33
TLR7 Q9NYK1 3/20 0.32
CNR1 P21554 1/20 0.32
CNR2 P34972 1/20 0.32
TRPC5 Q9UL62 1/20 0.31
ALDH1A1 P00352 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2D6 P10635 1/20 0.31
TSHR P16473 1/20 0.31
CYP2C19 P33261 1/20 0.31
PER2 O15055 1/20 0.31
CRY1 Q16526 1/20 0.31
CRY2 Q49AN0 1/20 0.31
TLR8 Q9NR97 1/20 0.31

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 SCHEMBL2414352 0.89 HIF1A (0.40) HIF1AKDM1AMAOAMAOBKCNH3
Iodide SCHEMBL13280558 0.79 HIF1A (0.48) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Iodide SCHEMBL1969660 0.76 HIF1A (0.44) HIF1AKDM1AMAOAMAOBALDH1A1
Bromide SCHEMBL129506 0.75 HIF1A (0.48) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Iodide SCHEMBL1968748 0.72 ALDH1A1 (0.35) HIF1AALDH1A1TSHR
Bromide SCHEMBL6428595 0.72 HIF1A (0.44) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Iodide SCHEMBL8182047 0.71 HIF1A (0.40) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Iodide SCHEMBL8182049 0.71 HIF1A (0.40) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL9822359 0.71 ALDH1A1 (0.39) HIF1AALDH1A1TSHR
SCHEMBL5269898 0.71 GBA1 (0.50) TSHR

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-20130102617-A1 METHOD OF TREATING DIABETES, METABOLIC SYNDROME AND OBESITY USING PHENYLACETAMIDE DERIVATIVE ASTELLAS PHARMA INC. (JP) 2013-04-25 US disclosed
US-8329707-B2 Substituted pyrazine compounds ASTELLAS PHARMA INC. (JP) 2012-12-11 US disclosed
US-20100286171-A1 PHENYLACETAMIDE DERIVATIVE ASTELLAS PHARMA INC. (JP) 2010-11-11 US disclosed
EP-2236498-A1 PHENYL ACETAMIDE DERIVATIVE Astellas Pharma Inc. (JP) 2010-10-06 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100286171-A1 PHENYLACETAMIDE DERIVATIVE AADAC, PGC, PC HIF1A 2722/4885KDM1A 1950/4885MAOA 1299/4885
US-20130102617-A1 METHOD OF TREATING DIABETES, METABOLIC SYNDROME AND OBESITY USING PHENYLACETAMIDE DERIVATIVE PC, PCK2, GCKR HIF1A 2150/4885KDM1A 2866/4885MAOA 1209/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.