Iodide

Iodide

SCHEMBL608287

CCCC(=O)SC(O)C[N+](C)(C)C.[I-]

nearest known ligand 0.35

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
MAPT P10636 5/20 0.35
SLC22A16 Q86VW1 1/20 0.35
CYP1A2 P05177 3/20 0.35
MAPK1 P28482 4/20 0.34
MEN1 O00255 3/20 0.34
GMNN O75496 3/20 0.34
LMNA P02545 3/20 0.34
KMT2A Q03164 3/20 0.34
NPSR1 Q6W5P4 3/20 0.34
TP53 P04637 3/20 0.34
TSHR P16473 3/20 0.34
HSP90AA1 P07900 2/20 0.34
BLM P54132 2/20 0.34
NR1H4 Q96RI1 2/20 0.34
CYP2C9 P11712 2/20 0.34
HIF1A Q16665 2/20 0.34
SLC25A20 O43772 3/20 0.33
CYP2D6 P10635 2/20 0.33
GLA P06280 1/20 0.33
PMP22 Q01453 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
SCHEMBL1902716 0.98 MAPT (0.36) MAPTSLC22A16CYP1A2MAPK1MEN1
SCHEMBL570499 0.98 MAPT (0.36) MAPTSLC22A16CYP1A2MAPK1MEN1
Hydrochloric Acid SCHEMBL8827832 0.96 MAPT (0.39) MAPTSLC22A16CYP1A2MAPK1MEN1
Hydrochloric Acid SCHEMBL5450059 0.96 MAPT (0.39) MAPTSLC22A16CYP1A2MAPK1MEN1
Iodide SCHEMBL5144330 0.84 MAPT (0.38) MAPTSLC22A16CYP1A2MEN1LMNA
SCHEMBL8055941 0.82 MAPT (0.39) MAPTSLC22A16CYP1A2MAPK1MEN1
SCHEMBL1057053 0.82 MAPT (0.39) MAPTSLC22A16CYP1A2MAPK1MEN1
Iodide SCHEMBL400576 0.75 MAPT (0.40) MAPTSLC22A16CYP1A2MEN1LMNA
SCHEMBL6153646 0.73 MAPT (0.41) MAPTSLC22A16CYP1A2MEN1LMNA
SCHEMBL77665 0.73 MAPT (0.41) MAPTSLC22A16CYP1A2MEN1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122060839-A Vegetable pesticide residue rapid screening and detecting method 云浮市云安区农业发展服务中心 2026-05-19 CN claimed
CN-119372283-B Cholinesterase determination reagent and application thereof 中生北控生物科技股份有限公司 2025-04-04 CN claimed
CN-119372283-A Cholinesterase determination reagent and application thereof 中生北控生物科技股份有限公司 2025-01-28 CN claimed
CN-115722210-B Recursive nanofiber-based detection material and preparation method and application thereof 广西大学 2024-02-20 CN claimed
CN-106680222-B Cholinesterase measures reagent and kit 郑州科欣生物技术有限公司 2019-05-28 CN claimed
CN-106680222-A Reagent for determining cholinesterase and kit 郑州科欣生物技术有限公司 2017-05-17 CN claimed
EP-2035032-A2 METHODS FOR ESTER DETOXICATION Human Biomolecular Research Institute (US) 2009-03-18 EP claimed
WO-2007146003-A2 METHODS FOR ESTER DETOXICATION HUMAN BIOMOLECULAR RESEARCH INSTITUTE (US) 2007-12-21 WO claimed
US-20070286846-A1 Novel methods for ester detoxication HUMAN BIOMOLECULAR RESEARCH INSTITUTE 2007-12-13 US claimed
US-6773822-B2 ANTIFUNGAL AGENT MAY BE PRESENT IN THE GYPSUM CORE AND/OR ON ONE OR BOTH OF THE PAPER FACINGS, AND MAY BE ENCAPSULATED IN A MATERIAL THAT RELEASES THE ANTIFUNGAL AGENT OVER TIME AND/OR UPON EXPOSURE TO MOISTURE. TEMPLE-INLAND FOREST PRODUCTS CORPORATION 2004-08-10 US claimed
EP-0533283-B1 Assay for serum cholinesterase acitivity JOHNSON & JOHNSON CLIN DIAG (US) 1996-12-11 EP claimed
US-5272061-A Assay for serum cholinesterase activity EASTMAN KODAK COMPANY (US) 1993-12-21 US claimed
EP-0533283-A1 Assay for serum cholinesterase acitivity Johnson & Johnson Clinical Diagnostics, Inc. (US) 1993-03-24 EP claimed
CN-122060839-A Vegetable pesticide residue rapid screening and detecting method 云浮市云安区农业发展服务中心 2026-05-19 CN disclosed
EP-4153561-B1 9H-FLUOREN DERIVATES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS UNIV JAGIELLONSKI (PL) 2026-04-29 EP disclosed
EP-4658639-A1 N,N-DIALKYL-4-(2-ETHYLINDAN-2-YL)-1H-IMIDAZOLE-1-CARBOXAMIDES AND RELATED COMPOUNDS FOR TREATMENT OF NEURODEGENERATIVE DISEASES Univerza V Ljubljani (SI) 2025-12-10 EP disclosed
EP-0083582-A4 IMMOBILIZED CHOLINESTERASE ENZYME PREPARATIONS AND A PROCESS FOR THE PREPARATION THEREOF. REANAL FINOMVEGYSZERGYAR (HU) 1984-01-31 EP disclosed
EP-0088636-A2 Quantitative analysis apparatus and method BIO-METRICS SYSTEMS, INC. (US) 1983-09-14 EP disclosed
EP-0083582-A1 IMMOBILIZED CHOLINESTERASE ENZYME PREPARATIONS AND A PROCESS FOR THE PREPARATION THEREOF. REANAL FINOMVEGYSZERGYAR (HU) 1983-07-20 EP disclosed
WO-1983000345-A1 IMMOBILIZED CHOLINESTERASE ENZYME PREPARATIONS AND A PROCESS FOR THE PREPARATION THEREOF BOROSS, László 1983-02-03 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 (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-20070286846-A1 Novel methods for ester detoxication CES2, BCHE, ACHE MAPT 2176/4885SLC22A16 1216/4885CYP1A2 25/4885

“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.