Iodide

Iodide

SCHEMBL17786154

CCCCCC[N+](C)(C)CCCNC(=O)CC[C@@H](C)[C@H]1CCC2C3CCC4CCCC[C@]4(C)C3CC[C@@]21C.[I-]

nearest known ligand 0.69

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
EPHA2 P29317 3/20 0.69
GPBAR1 Q8TDU6 9/20 0.60
AKR1B10 O60218 1/20 0.60
AKR1B1 P15121 1/20 0.60
EFNA1 P20827 1/20 0.60
PSEN1 P49768 1/20 0.60
PSEN2 P49810 1/20 0.60
APH1B Q8WW43 1/20 0.60
NCSTN Q92542 1/20 0.60
APH1A Q96BI3 1/20 0.60
PSENEN Q9NZ42 1/20 0.60
MEN1 O00255 1/20 0.60
LMNA P02545 1/20 0.60
KMT2A Q03164 1/20 0.60
HSD17B10 Q99714 1/20 0.60
TDP1 Q9NUW8 1/20 0.60
VDR P11473 2/20 0.53
ABCC4 O15439 2/20 0.53
NR1H4 Q96RI1 1/20 0.51
USP2 O75604 1/20 0.50

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 SCHEMBL17786188 1.00 EPHA2 (0.69) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL21878954 1.00 EPHA2 (0.69) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786186 1.00 EPHA2 (0.69) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786155 1.00 EPHA2 (0.69) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786150 0.99 EPHA2 (0.70) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786149 0.99 EPHA2 (0.70) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786157 0.97 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786159 0.97 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786177 0.95 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786176 0.95 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11629166-B2 Compound for treating clostridium difficile ASTON UNIVERSITY (GB) 2023-04-18 US disclosed
US-20200131223-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE INSIGHT HEALTH LIMITED 2020-04-30 US disclosed
US-20170320906-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE INSIGHT HEALTH LIMITED (GB) 2017-11-09 US disclosed
EP-3223855-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE Aston University (GB) 2017-10-04 EP disclosed
WO-2016083819-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE ASTON UNIVERSITY (GB) 2016-06-02 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 (3 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-11629166-B2 Compound for treating clostridium difficile DSTN, DAD1, DDOST EPHA2 1043/4885GPBAR1 77/4885AKR1B10 2810/4885
US-20170320906-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE DSTN, DAD1, DDOST EPHA2 1043/4885GPBAR1 77/4885AKR1B10 2810/4885
US-20200131223-A1 COMPOUND FOR TREATING CLOSTRIDIUM DIFFICILE DSTN, DAD1, DDOST EPHA2 1043/4885GPBAR1 77/4885AKR1B10 2810/4885

“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.