Iodide

Iodide

SCHEMBL4336770

CCc1ccc(C)[n+](CC)c1.[I-]

nearest known ligand 0.39

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
SMN1; SMN2 Q16637 2/20 0.39
LMNA P02545 2/20 0.39
KDM4E B2RXH2 1/20 0.39
MEN1 O00255 1/20 0.39
APOBEC3A P31941 1/20 0.39
HTT P42858 1/20 0.39
KMT2A Q03164 1/20 0.39
APOBEC3G Q9HC16 1/20 0.39
CA2 P00918 1/20 0.38
TP53 P04637 2/20 0.37
TAAR1 Q96RJ0 1/20 0.37
CYP2A6 P11509 1/20 0.35
LPL P06858 1/20 0.35
LIPG Q9Y5X9 1/20 0.35
ALDH1A1 P00352 1/20 0.34
TSHR P16473 1/20 0.33
MAPK1 P28482 1/20 0.33
ATM Q13315 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33

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
SCHEMBL641259 0.98 CA2 (0.39) SMN1; SMN2LMNAKDM4EMEN1APOBEC3A
SCHEMBL29561231 0.98 CA2 (0.39) SMN1; SMN2LMNAKDM4EMEN1APOBEC3A
Bromide SCHEMBL11435482 0.96 CA2 (0.38) SMN1; SMN2LMNAKDM4EMEN1APOBEC3A
Bromide SCHEMBL10844297 0.79 CA2 (0.35) SMN1; SMN2LMNACA2TP53TAAR1
Hydrochloric Acid SCHEMBL11428178 0.76 LPL (0.35) SMN1; SMN2CA2TP53TAAR1CYP2A6
SCHEMBL8723606 0.76 KDM4E (0.36) SMN1; SMN2LMNAKDM4EMEN1APOBEC3A
Iodide SCHEMBL3862124 0.76 CA2 (0.39) SMN1; SMN2LMNACA2TP53TAAR1
SCHEMBL1105765 0.75 LMNA (0.43) SMN1; SMN2LMNAKDM4EMEN1APOBEC3A
Iodide SCHEMBL3317180 0.74 CA2 (0.42) SMN1; SMN2LMNACA2TP53TAAR1
Bromide SCHEMBL10858949 0.74 SMN1; SMN2 (0.44) SMN1; SMN2LMNAKDM4EMEN1HTT

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-7629491-B2 Hydrocarboxylation process EASTMAN CHEMICAL COMPANY (US) 2009-12-08 US disclosed
US-20070299280-A1 forming propionic acid from ethylene, water and carbon monoxide; not using the hazardous and corrosive hydrogen halides or sulfonic acids; free of hydrogen iodide and/or ethyl iodide; no diethyl ketone by-products EASTMAN CHEMICAL COMPANY (US) 2007-12-27 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-20070299280-A1 forming propionic acid from ethylene, water and carbon monoxide; not using the hazardous and corrosive hydrogen halides or sulfonic acids; free of hydrogen iodide and/or ethyl iodide; no diethyl ketone by-products ETV6, ETV1, HAO2 SMN1; SMN2 3854/4885LMNA 4077/4885KDM4E 2451/4885

“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.