Iodide

Iodide

SCHEMBL3474173

CCCn1ccnc1C.CCCn1ccnc1C.I.I.I.I

nearest known ligand 0.74

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 0.74
KMT2A Q03164 2/20 0.74
POLB P06746 1/20 0.74
TSHR P16473 1/20 0.51
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
CA9 Q16790 1/20 0.47
TLR8 Q9NR97 2/20 0.44
FDPS P14324 1/20 0.43
LMNA P02545 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
P2RX7 Q99572 1/20 0.40
CYP1A2 P05177 1/20 0.39
CYP3A4 P08684 1/20 0.39
CYP2D6 P10635 1/20 0.39
CYP19A1 P11511 1/20 0.39
CYP2C9 P11712 1/20 0.39
CYP2C19 P33261 1/20 0.39
KDM4E B2RXH2 1/20 0.38

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 SCHEMBL876466 1.00 ALDH1A1 (0.74) ALDH1A1KMT2APOLBTSHRCA12
Iodide SCHEMBL5538014 1.00 ALDH1A1 (0.74) ALDH1A1KMT2APOLBTSHRCA12
Iodide SCHEMBL5533691 1.00 ALDH1A1 (0.74) ALDH1A1KMT2APOLBTSHRCA12
SCHEMBL82664 0.98
Hydrochloric Acid SCHEMBL28763275 0.96 KMT2A (0.74) ALDH1A1KMT2APOLBTSHRCA12
Hydrochloric Acid SCHEMBL28337026 0.96 KMT2A (0.74) ALDH1A1KMT2APOLBTSHRCA12
Bromide SCHEMBL28812312 0.96 ALDH1A1 (0.74) ALDH1A1KMT2APOLBTSHRCA12
Ammonia Solution, Strong SCHEMBL14645160 0.96 ALDH1A1 (0.74) ALDH1A1KMT2APOLBTSHRCA12
Dimethylamine SCHEMBL8078055 0.92 KMT2A (0.69) ALDH1A1KMT2APOLBTSHRCA12
Iodide SCHEMBL1226180 0.88 ALDH1A1 (0.96) ALDH1A1KMT2APOLBTSHRCA12

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
WO-2010088723-A1 DYE COMPOSITION FOR USE IN PHOTOELECTRIC MATERIAL UNIVERSITY OF WOLLONGONG (AU) 2010-08-12 WO disclosed
US-20070017569-A1 Metal complex compositions and use thereof in dye sensitized solar cells GENERAL ELECTRIC COMPANY 2007-01-25 US disclosed
EP-1630883-A2 Molecular photovoltaics GENERAL ELECTRIC COMPANY (US) 2006-03-01 EP disclosed
US-20060021647-A1 Molecular photovoltaics, method of manufacture and articles derived therefrom SABIC INNOVATIVE PLASTICS IP B.V. 2006-02-02 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-20070017569-A1 Metal complex compositions and use thereof in dye sensitized solar cells TST, SPR, TYR ALDH1A1 847/4885KMT2A 852/4885POLB 4019/4885

“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.