Iodide

Iodide

SCHEMBL3972002

Cc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)o1.[I-]

nearest known ligand 0.44

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
CHRM1 known ✓ P11229 1/20 0.41
CHRM3 known ✓ P20309 1/20 0.41
MAPT P10636 4/20 0.44
CHRM2 P08172 2/20 0.41
MEN1 O00255 1/20 0.41
CHRM4 P08173 1/20 0.41
CHRM5 P08912 1/20 0.41
CYP2C9 P11712 1/20 0.41
KMT2A Q03164 1/20 0.41
HIF1A Q16665 1/20 0.40
SNCA P37840 2/20 0.37
POLB P06746 2/20 0.37
TDP1 Q9NUW8 1/20 0.36
NPC1 O15118 2/20 0.35
RAB9A P51151 2/20 0.35
PKM P14618 2/20 0.34
MAPK1 P28482 2/20 0.34
CTDSP1 Q9GZU7 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
ALOX5 P09917 1/20 0.34

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 SCHEMBL11464816 0.76 MAPT (0.38) MAPTCHRM2MEN1CHRM4CHRM5
Hydrochloric Acid SCHEMBL17078920 0.70 ALDH1A1 (0.49) MAPTMEN1CYP2C9KMT2AHIF1A
Bromide SCHEMBL386471 0.69 HIF1A (0.43) MAPTCHRM2MEN1KMT2AHIF1A
SCHEMBL3180066 0.68 CHRM2 (0.47) MAPTCHRM2MEN1CHRM4CHRM5
SCHEMBL15371816 0.68 CHRM2 (0.47) MAPTCHRM2MEN1CHRM4CHRM5
SCHEMBL104309 0.67 CHRM2 (0.50) MAPTCHRM2MEN1CHRM4CHRM5
Hydrochloric Acid SCHEMBL10891834 0.67 NPBWR1 (0.51) MAPTMEN1KMT2AHIF1ASNCA
Iodide SCHEMBL159922 0.66 SNCA (0.63) HIF1ASNCAALDH1A1TSHR
Iodide SCHEMBL9321342 0.66 SNCA (0.69) HIF1ASNCAALDH1A1TSHR
Bromide SCHEMBL11159330 0.66 HIF1A (0.39) MEN1KMT2AHIF1ASNCATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7547790-B2 Optically active 4,4-di-substituted oxazolidine derivative and method for producing same SANKYO COMPANY, LIMITED (JP) 2009-06-16 US disclosed
US-20080108828-A1 Optically Active 4,4-Di-Substituted Oxazolidine Derivative and Method for Producing Same SANKYO COMPANY, LIMITED (JP) 2008-05-08 US 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 (1 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-20080108828-A1 Optically Active 4,4-Di-Substituted Oxazolidine Derivative and Method for Producing Same CBR3, C9, COX6C CHRM1 214/4885CHRM3 726/4885MAPT 4145/4885

“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.