Iodide

Iodide

SCHEMBL2795262

CC[n+]1ccn(CCCOC(=O)[C@](O)(c2ccccc2)[C@@H]2CCC(F)(F)C2)c1C.[I-]

nearest known ligand 0.44

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 4)

geneUniProtsupporting neighboursconfidence
CHRM1 known ✓ P11229 18/20 0.43
CHRM3 known ✓ P20309 18/20 0.43
HTT P42858 1/20 0.44
CHRM2 P08172 18/20 0.43

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
Bromide SCHEMBL2797662 0.98 HTT (0.44) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2796791 0.94 HTT (0.47) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2797766 0.93 CHRM2 (0.45) CHRM2CHRM1CHRM3
Bromide SCHEMBL2845629 0.93 CHRM2 (0.45) CHRM2CHRM1CHRM3
Bromide SCHEMBL2798493 0.93 CHRM2 (0.45) CHRM2CHRM1CHRM3
Bromide SCHEMBL2795582 0.93 HTT (0.43) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2796086 0.93 HTT (0.43) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2792277 0.92 HTT (0.43) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2794478 0.92 HTT (0.43) HTTCHRM2CHRM1CHRM3
Bromide SCHEMBL2794159 0.91 HTT (0.42) HTTCHRM2CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100168197-A1 MUSCARINIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2010-07-01 US claimed
US-20100004215-A1 COMPOSITIONS OF PHOSPHODIESTERASE TYPE IV INHIBITORS RANBAXY LABORATORIES LIMITED (IN) 2010-01-07 US claimed
EP-2111861-A1 Compositions of phosphodiesterase type IV inhibitors Ranbaxy Laboratories Limited (IN) 2009-10-28 EP claimed
US-20100168197-A1 MUSCARINIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2010-07-01 US disclosed
US-20100004215-A1 COMPOSITIONS OF PHOSPHODIESTERASE TYPE IV INHIBITORS RANBAXY LABORATORIES LIMITED (IN) 2010-01-07 US disclosed
EP-2111861-A1 Compositions of phosphodiesterase type IV inhibitors Ranbaxy Laboratories Limited (IN) 2009-10-28 EP 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 (2 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-20100168197-A1 MUSCARINIC RECEPTOR ANTAGONISTS CHRM3, CHRM5, CHRM2 CHRM1 5/4885CHRM3 1/4885HTT 3592/4885
US-20100004215-A1 COMPOSITIONS OF PHOSPHODIESTERASE TYPE IV INHIBITORS PDE4B, PDE4A, PDE3B CHRM1 158/4885CHRM3 88/4885HTT 4847/4885

“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.