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)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CALM1 | P0DP23 | 1/20 | 0.47 |
| ▸ | TSHR | P16473 | 4/20 | 0.43 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.43 |
| ▸ | IDO1 | P14902 | 3/20 | 0.43 |
| ▸ | LOXL2 | Q9Y4K0 | 2/20 | 0.43 |
| ▸ | TP53 | P04637 | 1/20 | 0.43 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.43 |
| ▸ | MAOB | P27338 | 1/20 | 0.41 |
| ▸ | HPGD | P15428 | 1/20 | 0.41 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.41 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.41 |
| ▸ | CASP1 | P29466 | 1/20 | 0.41 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.41 |
| ▸ | TAAR1 | Q96RJ0 | 2/20 | 0.40 |
| ▸ | CA1 | P00915 | 1/20 | 0.40 |
| ▸ | CA2 | P00918 | 1/20 | 0.40 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.39 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.39 |
| ▸ | HTR2A | P28223 | 1/20 | 0.39 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.39 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Water SCHEMBL7540197 | 0.94 | CALM1 (0.47) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Hydrochloric Acid SCHEMBL1030799 | 0.94 | CALM1 (0.47) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Fluoride Ion SCHEMBL5897693 | 0.94 | CALM1 (0.47) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Bromide SCHEMBL5897988 | 0.94 | CALM1 (0.47) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| SCHEMBL11787603 | 0.94 | CALM1 (0.47) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Hydrochloric Acid SCHEMBL8855132 | 0.75 | CALM1 (0.41) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| SCHEMBL3747885 | 0.67 | — | — | |
| Diphenylmethane SCHEMBL1303 | 0.65 | CALM1 (1.00) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Diphenylmethane SCHEMBL3792579 | 0.65 | CALM1 (1.00) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| SCHEMBL62125 | 0.65 | ALDH1A1 (0.69) | CALM1ALDH1A1LOXL2MAOBHPGD |
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 63 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7008899-B2 | Lanthanide-based catalyst composition for producing cis-1,4-polydienes | BRIDGESTONE CORPORATION (JP) | 2006-03-07 | — | — | US | claimed |
| US-20050038215-A1 | Lanthanide-based catalyst composition for producing cis-1,4-polydienes | BRIDGESTONE CORPORATION (JP) | 2005-02-17 | — | — | US | claimed |
| US-6395912-B1 | ISOMERIZATION OF EPOXY COMPOUND | EASTMAN CHEMICAL COMPANY | 2002-05-28 | — | — | US | claimed |
| US-6335455-B1 | FROM GAMMA, DELTA-EPOXYALKENES | EASTMAN CHEMICAL COMPANY | 2002-01-01 | — | — | US | claimed |
| EP-1049688-B1 | PROCESS FOR THE PRODUCTION OF 2,5-DIHYDROFURAN | EASTMAN CHEM CO (US) | 2001-09-12 | — | — | EP | claimed |
| EP-1049688-A1 | PROCESS FOR THE PRODUCTION OF 2,5-DIHYDROFURAN | EASTMAN CHEMICAL COMPANY (US) | 2000-11-08 | — | — | EP | claimed |
| WO-1999035137-A1 | PROCESS FOR THE PRODUCTION OF 2,5-DIHYDROFURAN | EASTMAN CHEMICAL COMPANY (US) | 1999-07-15 | — | — | WO | claimed |
| US-20150080581-A1 | MULTICOORDINATED METAL COMPLEXES FOR USE IN METATHESIS REACTIONS | RIMTEC CORPORATION (JP) | 2015-03-19 | — | — | US | disclosed |
| US-8927670-B2 | Multicoordinated metal complexes for use in metathesis reactions | RIMTEC CORPORATION (JP) | 2015-01-06 | — | — | US | disclosed |
| EP-2397475-B1 | 4, 4' disubstituted 4H-cyclopentadithiophene and new methods for synthesising the same | IMEC (BE) | 2014-11-12 | — | — | EP | disclosed |
| US-8765882-B2 | Polythiophene based active layer for solar cells | IMEC (BE) | 2014-07-01 | — | — | US | disclosed |
| US-8450604-B2 | Polymerisable compounds for making opto-electronic devices | IMEC (BE) | 2013-05-28 | — | — | US | disclosed |
| US-8329923-B2 | 4, 4′ disubstituted 4H-cyclopentadithiophene and new methods for synthesizing the same | IMEC (BE) | 2012-12-11 | — | — | US | disclosed |
| WO-1994003272-A1 | PROCESS FOR THE SEPARATION OF OLIGOMERIC MATERIALS FROM A CATALYST MIXTURE | EASTMAN CHEMICAL COMPANY (US) | 1994-02-17 | — | — | WO | disclosed |
| US-5238889-A | Solvent extraction | EASTMAN KODAK COMPANY (US) | 1993-08-24 | — | — | US | disclosed |
| WO-1993010111-A1 | CONTINUOUS PROCESS FOR THE MANUFACTURE OF 2,5-DIHYDROFURANS FROM η,δ-EPOXYBUTENES | EASTMAN KODAK COMPANY (US) | 1993-05-27 | — | — | WO | disclosed |
| EP-0518973-A1 | ISOMERIZATION OF EPOXYALKENES TO 2,5-DIHYDROFURANS AND CATALYSTS COMPOSITIONS USEFUL THEREFOR. | EASTMAN KODAK CO (US) | 1992-12-23 | — | — | EP | disclosed |
| US-5082956-A | Quaternary onium iodide catalyst | EASTMAN KODAK COMPANY (US) | 1992-01-21 | — | — | US | disclosed |
| WO-1991013882-A1 | ISOMERIZATION OF EPOXYALKENES TO 2,5-DIHYDROFURANS AND CATALYSTS COMPOSITIONS USEFUL THEREFOR | EASTMAN KODAK COMPANY (US) | 1991-09-19 | — | — | WO | disclosed |
| US-4148814-A | Process for preparing monohydrocarbyltin trihalides | PENNWALT CORPORATION (US) | 1979-04-10 | — | — | 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 (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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20150080581-A1 | MULTICOORDINATED METAL COMPLEXES FOR USE IN METATHESIS REACTIONS | APEX1, SOD1, AP1M1 | CALM1 4108/4885TSHR 4417/4885ALDH1A1 1713/4885 |
“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.