Iodide

Iodide

SCHEMBL3858577

CCCCCCCCCCCC[P+](CCCC)(CCCCCCCCCCCC)CCCCCCCCCCCC.[I-]

nearest known ligand 0.94

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 8)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 7/20 0.94
TSHR P16473 2/20 0.50
THRB P10828 1/20 0.50
LMNA P02545 1/20 0.42
BDKRB2 P30411 3/20 0.41
CA2 P00918 1/20 0.39
OPRM1 P35372 1/20 0.39
ALDH1A1 P00352 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 SCHEMBL5091656 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5088416 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5085198 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5091864 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5087203 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5087043 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5086658 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5088125 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5085433 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2
Iodide SCHEMBL5091621 1.00 DNM1 (0.94) DNM1TSHRTHRBLMNABDKRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9238606-B1 Methyl-Iodide-free carbonylation of methanol to acetaldehyde EASTMAN CHEMICAL COMPANY (US) 2016-01-19 US claimed
EP-1501779-B1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEM CO (US) 2009-12-23 EP claimed
EP-1501779-A1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2005-02-02 EP claimed
WO-2003093211-A1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2003-11-13 WO claimed
US-20030212295-A1 Continuous carbonylation process EASTMAN CHEMICAL COMPANY 2003-11-13 US claimed
US-6395912-B1 ISOMERIZATION OF EPOXY COMPOUND EASTMAN CHEMICAL COMPANY 2002-05-28 US claimed
US-6342614-B1 ISOMERIZATION OF GAMMA, DELTA-EPOXYALKENES OR GAMMA, DELTA-EPOXYCYCLOALKENES TO 2,5-DIHYDROFURANS USING CATALYTIC SYSTEM WHICH COMPRISES ONIUM IODIDE AND LEWIS ACID EASTMAN CHEMICAL COMPANY 2002-01-29 US claimed
US-9266807-B1 Conversion of alcohols to longer chain aldehydes or alcohols EASTMAN CHEMICAL COMPANY (US) 2016-02-23 US disclosed
US-9238606-B1 Methyl-Iodide-free carbonylation of methanol to acetaldehyde EASTMAN CHEMICAL COMPANY (US) 2016-01-19 US disclosed
EP-1501779-B1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEM CO (US) 2009-12-23 EP disclosed
US-7629491-B2 Hydrocarboxylation process EASTMAN CHEMICAL COMPANY (US) 2009-12-08 US disclosed
WO-2009123675-A1 IMPROVED CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2009-10-08 WO disclosed
US-20090247783-A1 CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2009-10-01 US disclosed
US-7582792-B2 Carbonylation process EASTMAN CHEMICAL COMPANY (US) 2009-09-01 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
US-20070293695-A1 CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2007-12-20 US disclosed
US-6916951-B2 Continuous carbonylation process EASTMAN CHEMICAL COMPANY (US) 2005-07-12 US disclosed
EP-1501779-A1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2005-02-02 EP disclosed
WO-2003093211-A1 CONTINUOUS CARBONYLATION PROCESS EASTMAN CHEMICAL COMPANY (US) 2003-11-13 WO disclosed
US-20030212295-A1 Continuous carbonylation process EASTMAN CHEMICAL COMPANY 2003-11-13 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 (4 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-20070293695-A1 CARBONYLATION PROCESS CBR3, HAO2, CA4 DNM1 3533/4885TSHR 1538/4885THRB 1030/4885
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 DNM1 985/4885TSHR 2619/4885THRB 1693/4885
US-20090247783-A1 CARBONYLATION PROCESS CA4, HAO2, CA9 DNM1 2159/4885TSHR 1657/4885THRB 1556/4885
US-20030212295-A1 Continuous carbonylation process CA4, CA5B, CA14 DNM1 2851/4885TSHR 4418/4885THRB 4711/4885

“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.