Iodide

Iodide

SCHEMBL18074423

C[n+]1ccc(/C=N/N(CCCN)c2ccccc2)cc1.[I-]

nearest known ligand 0.43

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
▸ ACHE known ✓ P22303 1/20 0.37
▸ ALDH1A1 P00352 6/20 0.43
▸ MEN1 O00255 5/20 0.43
▸ KMT2A Q03164 5/20 0.43
▸ SMN1; SMN2 Q16637 2/20 0.43
▸ MCL1 Q07820 1/20 0.43
▸ CHAT P28329 3/20 0.41
▸ MAPT P10636 6/20 0.41
▸ HSP90AA1 P07900 1/20 0.41
▸ GAA P10253 1/20 0.41
▸ LMNA P02545 4/20 0.36
▸ MAPK1 P28482 3/20 0.36
▸ POLB P06746 1/20 0.36
▸ PKM P14618 1/20 0.36
▸ ALPG P10696 1/20 0.35
▸ THRB P10828 1/20 0.35
▸ HTT P42858 1/20 0.35
▸ GFER P55789 1/20 0.35
▸ NPSR1 Q6W5P4 1/20 0.35
▸ ADRA2C P18825 1/20 0.35

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 SCHEMBL18074426 1.00 ALDH1A1 (0.43) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
SCHEMBL18087744 0.99 MEN1 (0.44) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
Iodide SCHEMBL18063101 0.95 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
Iodide SCHEMBL18063102 0.95 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
SCHEMBL18087437 0.93 MEN1 (0.42) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
SCHEMBL28017973 0.86 ALDH1A1 (0.47) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
SCHEMBL18087439 0.85 MEN1 (0.40) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
Bromide SCHEMBL18062947 0.84 ACHE (0.40) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
Bromide SCHEMBL18062948 0.84 ACHE (0.40) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1
SCHEMBL18087718 0.84 KMT2A (0.47) ALDH1A1MEN1KMT2ASMN1; SMN2MCL1

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
EP-3271423-B1 CATIONIC DIRECT DYES BASF SE (DE) 2022-08-31 — — EP disclosed
US-20180244924-A1 Cationic Direct Dyes BASF SE (DE) 2018-08-30 — — US disclosed
EP-3271423-A1 CATIONIC DIRECT DYES BASF SE (DE) 2018-01-24 — — EP disclosed
WO-2016146813-A1 CATIONIC DIRECT DYES BASF SE (DE) 2016-09-22 — — 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-20180244924-A1 Cationic Direct Dyes H1-0, TPH1, H1-2 ACHE 2316/4885ALDH1A1 39/4885MEN1 146/4885

“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.

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