Iodide

Iodide

SCHEMBL3974532

CCCCP(CCCC)CCCC.I

nearest known ligand 0.43

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 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.43
LMNA P02545 3/20 0.43
THRB P10828 1/20 0.40
DNM1 Q05193 5/20 0.33
ALDH1A1 P00352 4/20 0.33
TDP1 Q9NUW8 1/20 0.33
SLC22A1 O15245 2/20 0.32
SLC22A2 O15244 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HSD17B10 Q99714 1/20 0.30
MEN1 O00255 1/20 0.30
KMT2A Q03164 1/20 0.30

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 SCHEMBL28614857 1.00 TSHR (0.43) TSHRLMNATHRBDNM1ALDH1A1
Hydrochloric Acid SCHEMBL7138382 0.96 TSHR (0.40) TSHRLMNATHRBDNM1ALDH1A1
Iodide SCHEMBL10682603 0.96 TSHR (0.40) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL7874985 0.96 TSHR (0.46) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL821221 0.96 TSHR (0.46) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL6033 0.96 TSHR (0.46) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL3110104 0.92 TSHR (0.43) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL7631534 0.92 TSHR (0.43) TSHRLMNATHRBDNM1ALDH1A1
Hydrochloric Acid SCHEMBL108265 0.92 TSHR (0.43) TSHRLMNATHRBDNM1ALDH1A1
SCHEMBL15656735 0.92 TSHR (0.43) TSHRLMNATHRBDNM1ALDH1A1

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10544299-B2 Vinyl-containing compounds with high heat distortion REICHHOLD LLC 2 (US) 2020-01-28 US claimed
WO-2014099376-A1 VINYL CONTAINING COMPOUNDS WITH HIGH HEAT DISTORTION REICHHOLD, INC. (US) 2014-06-26 WO claimed
US-20140171568-A1 VINYL-CONTAINING COMPOUNDS WITH HIGH HEAT DISTORTION Polynt Composites USA Inc. 2014-06-19 US claimed
CN-115155656-A Catalyst for synthesizing cyclic carbonate and synthetic method of cyclic carbonate 深圳新宙邦科技股份有限公司 2022-10-11 CN disclosed
US-10962703-B1 Nanoparticle dispersion for increasing optical index of refraction FACEBOOK TECHNOLOGIES, LLC (US) 2021-03-30 US disclosed
US-10544299-B2 Vinyl-containing compounds with high heat distortion REICHHOLD LLC 2 (US) 2020-01-28 US disclosed
EP-3002312-B1 CURABLE COMPOSITIONS REICHHOLD LLC 2 (US) 2018-08-29 EP disclosed
US-20180223039-A1 CURABLE COMPOSITIONS REICHHOLD LLC 2 2018-08-09 US disclosed
US-10000602-B2 Curable compositions REICHHOLD LLC 2 (US) 2018-06-19 US disclosed
US-20160096918-A1 CURABLE COMPOSITIONS Polynt Composites USA Inc. 2016-04-07 US disclosed
EP-3002312-A1 CURABLE COMPOSITIONS Reichhold LLC 2 (US) 2016-04-06 EP disclosed
US-20080317877-A1 Biofilm Remover WHITELEY CORPORATION PTY. LTD. (AU) 2008-12-25 US disclosed
US-20080108828-A1 Optically Active 4,4-Di-Substituted Oxazolidine Derivative and Method for Producing Same SANKYO COMPANY, LIMITED (JP) 2008-05-08 US disclosed
EP-1806344-A1 OPTICALLY ACTIVE 4,4-DISUBSTITUTED OXAZOLIDINE DERIVATIVE AND METHOD FOR PRODUCING SAME Sankyo Company, Limited (JP) 2007-07-11 EP disclosed
WO-2001027183-A1 PREPARATION OF ACRYLIC COMPOUNDS CONTAINING RESINS WITH VINYL FUNCTIONALITY REICHHOLD, INC. (US) 2001-04-19 WO disclosed
US-5998568-A REACTING POLYALCOHOL OR POLYTHIOL WITH CYCLIC CARBONATE IN PRESENCE OF A CATALYST REICHHOLD, INC. (US) 1999-12-07 US disclosed
EP-0002590-B1 NOVEL PROSTAGLANDIN COMPOUNDS, PROCESSES FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AMERICAN CYANAMID COMPANY (US) 1981-09-30 EP disclosed
US-4230879-A 15-Deoxy-16-hydroxy-16-formyo or dimethoxy-methyl-prostane derivatives of the E and F series AMERICAN CYANAMID COMPANY (US) 1980-10-28 US disclosed
US-4227011-A 15-Deoxy-16-hydroxy-16-chloromethyl or bromomethyl prostaglandins of the E and F series AMERICAN CYANAMID COMPANY (US) 1980-10-07 US disclosed
EP-0013107-A1 16-Hydroxy-16-vinyl (or cyclopropyl)-prostan-1-ols and pharmaceutical compositions containing the same AMERICAN CYANAMID COMPANY (US) 1980-07-09 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 (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-20080108828-A1 Optically Active 4,4-Di-Substituted Oxazolidine Derivative and Method for Producing Same CBR3, C9, COX6C TSHR 1739/4885LMNA 2710/4885THRB 2917/4885

“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.