Iodide

Iodide

SCHEMBL1770191

Cc1nc2c(C)cccc2s1.I

nearest known ligand 0.63

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
ALDH1A1 P00352 3/20 0.63
MAPT P10636 5/20 0.49
PKM P14618 1/20 0.46
GAA P10253 2/20 0.45
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
MEN1 O00255 5/20 0.42
KMT2A Q03164 5/20 0.42
KDM4E B2RXH2 3/20 0.42
ALOX15 P16050 2/20 0.42
HPGD P15428 2/20 0.42
POLB P06746 2/20 0.42
L3MBTL1 Q9Y468 2/20 0.42
LMNA P02545 2/20 0.42
USP2 O75604 1/20 0.42
MCL1 Q07820 1/20 0.42
ESR2 Q92731 1/20 0.42
HSD17B10 Q99714 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
MAPK1 P28482 1/20 0.42

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
SCHEMBL1748098 0.98 ALDH1A1 (0.66) ALDH1A1MAPTPKMGAANPC1
Ammonia Solution, Strong SCHEMBL26679975 0.96 ALDH1A1 (0.63) ALDH1A1MAPTPKMGAANPC1
Hydrochloric Acid SCHEMBL28519025 0.94 ALDH1A1 (0.61) ALDH1A1MAPTPKMGAANPC1
SCHEMBL27849608 0.92 ALDH1A1 (0.65) ALDH1A1MAPTPKMGAANPC1
Formamide SCHEMBL28482328 0.87 ALDH1A1 (0.59) ALDH1A1MAPTPKMGAANPC1
SCHEMBL28158484 0.82 MAPT (0.52) ALDH1A1MAPTPKMGAAMEN1
SCHEMBL3918916 0.79 ALDH1A1 (0.63) ALDH1A1MAPTPKMGAANPC1
SCHEMBL14127197 0.79 ALDH1A1 (0.63) ALDH1A1MAPTPKMGAANPC1
SCHEMBL316414 0.78 ALDH1A1 (0.43) ALDH1A1MAPTPKMGAANPC1
SCHEMBL11120842 0.78 ALDH1A1 (0.61) ALDH1A1MAPTPKMGAANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119264097-A Fluorescent probe for monitoring FAO level of living cells and macrophage polarization phenotype, and preparation method and application thereof 贵州医科大学 2025-01-07 CN disclosed
CN-105203512-B A kind of carbazoles fluorescence probe and its preparation method and application 山西大学 2018-02-06 CN disclosed
US-20110112149-A1 EPOTHILONE ANALOGUES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR USE AND THEIR PREPA RATIONS TANG, LI (CN) 2011-05-12 US disclosed
EP-2261221-A1 EPOTHILONE ANALOGUES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR USE AND THEIR PREPARATIONS Tang, Li (CN) 2010-12-15 EP disclosed
CN-1234026-C Electric filter for electronic display KYOWA YUKA KK (JP) 2005-12-28 CN disclosed
CN-1435700-A Electric filter for electronic display KYOWA YUKA KK (JP) 2003-08-13 CN 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-20110112149-A1 EPOTHILONE ANALOGUES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR USE AND THEIR PREPA RATIONS PPIA, PREP, THPO ALDH1A1 2189/4885MAPT 3448/4885PKM 75/4885

“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.