Iodide

Iodide

SCHEMBL5564435

CCCCCC[n+]1cc(-c2ccccc2)cc(N2CCOCC2)n1.[I-]

nearest known ligand 0.47

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
MAPT P10636 3/20 0.47
ALDH1A1 P00352 3/20 0.47
HTT P42858 1/20 0.42
MTOR P42345 1/20 0.40
NPSR1 Q6W5P4 2/20 0.40
TSHR P16473 1/20 0.40
MAPK1 P28482 1/20 0.40
HSD17B10 Q99714 1/20 0.40
KMT2A Q03164 3/20 0.39
LMNA P02545 1/20 0.39
DGAT1 O75907 2/20 0.39
SOAT1 P35610 1/20 0.39
SMG1 Q96Q15 1/20 0.38
SMN1; SMN2 Q16637 3/20 0.37
MEN1 O00255 2/20 0.37
CYP1A2 P05177 1/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
ATR Q13535 1/20 0.37
NAPEPLD Q6IQ20 1/20 0.37

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 SCHEMBL5564583 0.99 MAPT (0.48) MAPTALDH1A1HTTMTORNPSR1
Bromide SCHEMBL6017404 0.97 MAPT (0.46) MAPTALDH1A1HTTMTORNPSR1
Iodide SCHEMBL5461872 0.95 MAPT (0.49) MAPTALDH1A1HTTMTORNPSR1
Iodide SCHEMBL5559595 0.91 ALDH1A1 (0.51) MAPTALDH1A1HTTMTORNPSR1
Iodide SCHEMBL5564559 0.86 HTT (0.44) MAPTALDH1A1HTTMTORNPSR1
Bromide SCHEMBL5559239 0.83 ALDH1A1 (0.59) MAPTALDH1A1HTTMTORNPSR1
Bromide SCHEMBL5559995 0.81 HTT (0.45) MAPTALDH1A1HTTMTORNPSR1
Bromide SCHEMBL5565800 0.79 HTT (0.48) MAPTALDH1A1HTTMTORNPSR1
Bromide SCHEMBL5460456 0.79 HTT (0.43) MAPTALDH1A1HTTMTORNPSR1
Iodide SCHEMBL5565098 0.77 HTT (0.51) MAPTALDH1A1HTTMTORNPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7300932-B2 Pyrrolo[1,2-b]pyridazine derivatives JAPAN TOBACCO INC. (JP) 2007-11-27 US disclosed
EP-1653969-A4 PYRROLO 1,2-B PYRIDAZINE DERIVATIVES JAPAN TOBACCO INC (JP) 2006-12-20 EP disclosed
EP-1653969-A2 PYRROLO 1,2-B PYRIDAZINE DERIVATIVES Japan Tabacco Inc. (JP) 2006-05-10 EP disclosed
US-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism TULARIK INC. (US) 2005-03-31 US disclosed
WO-2005013907-A2 PYRROLO[1,2-B]PYRIDAZINE DERIVATIVES JAPAN TOBACCO INC. (JP) 2005-02-17 WO 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-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism PC, ACACB, ACAT1 MAPT 2498/4885ALDH1A1 978/4885HTT 894/4885

“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.