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 | |
|---|---|---|---|---|
| ▸ | ACHE known ✓ | P22303 | 1/20 | 0.33 |
| ▸ | TDP1 | Q9NUW8 | 4/20 | 0.39 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 5/20 | 0.38 |
| ▸ | TSHR | P16473 | 5/20 | 0.35 |
| ▸ | CA1 | P00915 | 2/20 | 0.33 |
| ▸ | CA2 | P00918 | 2/20 | 0.33 |
| ▸ | CA9 | Q16790 | 2/20 | 0.33 |
| ▸ | LMNA | P02545 | 2/20 | 0.33 |
| ▸ | ALOX12 | P18054 | 2/20 | 0.33 |
| ▸ | APOBEC3A | P31941 | 1/20 | 0.33 |
| ▸ | APOBEC3G | Q9HC16 | 1/20 | 0.33 |
| ▸ | CA12 | O43570 | 1/20 | 0.33 |
| ▸ | GLA | P06280 | 1/20 | 0.33 |
| ▸ | CA3 | P07451 | 1/20 | 0.33 |
| ▸ | CA4 | P22748 | 1/20 | 0.33 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.33 |
| ▸ | CA7 | P43166 | 1/20 | 0.33 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.32 |
| ▸ | MAPT | P10636 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| SCHEMBL29818354 | 0.96 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| Fluoride Ion SCHEMBL3907946 | 0.92 | ALDH1A1 (0.39) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| Bromide SCHEMBL624578 | 0.92 | TDP1 (0.39) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| Hydrochloric Acid SCHEMBL727707 | 0.92 | TDP1 (0.39) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| Water SCHEMBL6846782 | 0.92 | TDP1 (0.39) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| SCHEMBL28760744 | 0.83 | CYP3A4 (0.33) | TDP1CYP3A4ALDH1A1TSHR | |
| SCHEMBL28760731 | 0.83 | CYP3A4 (0.33) | TDP1CYP3A4ALDH1A1TSHR | |
| Iodide SCHEMBL5142121 | 0.72 | TSHR (0.37) | TDP1CYP3A4ALDH1A1TSHRCA1 | |
| Iodide SCHEMBL9805251 | 0.64 | — | — | |
| Iodide SCHEMBL2166396 | 0.61 | ALDH1A1 (0.39) | TDP1CYP3A4ALDH1A1TSHRCA1 |
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 42 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6395912-B1 | ISOMERIZATION OF EPOXY COMPOUND | EASTMAN CHEMICAL COMPANY | 2002-05-28 | — | — | US | claimed |
| US-10442872-B2 | Biosourced polymer for manufacturing, via catalytic carbonation, a non-bituminous polyhydroxyurethane binder for roadway or civil engineering-related uses | COLAS (FR) | 2019-10-15 | — | — | US | disclosed |
| US-20180037673-A1 | BIOSOURCED POLYMER FOR MANUFACTURING, VIA CATALYTIC CARBONATION, A NON-BITUMINOUS POLYHYDROXYURETHANE BINDER FOR ROADWAY OR CIVIL ENGINEERING-RELATED USES | COLAS (FR) | 2018-02-08 | — | — | US | disclosed |
| EP-2873661-B1 | Synthesis process of trimethylene carbonate from 1,3-propanediol and urea by heterogeneous catalysis | ARKEMA FRANCE (FR) | 2015-10-07 | — | — | EP | disclosed |
| EP-2873661-A1 | Synthesis process of trimethylene carbonate from 1,3-propanediol and urea by heterogeneous catalysis | ARKEMA FRANCE (FR) | 2015-05-20 | — | — | EP | disclosed |
| US-6395912-B1 | ISOMERIZATION OF EPOXY COMPOUND | EASTMAN CHEMICAL COMPANY | 2002-05-28 | — | — | US | disclosed |
| US-6342614-B1 | ISOMERIZATION OF GAMMA, DELTA-EPOXYALKENES OR GAMMA, DELTA-EPOXYCYCLOALKENES TO 2,5-DIHYDROFURANS USING CATALYTIC SYSTEM WHICH COMPRISES ONIUM IODIDE AND LEWIS ACID | EASTMAN CHEMICAL COMPANY | 2002-01-29 | — | — | US | disclosed |
| US-6201138-B1 | CONTACTING A GAMMA, DELTA-EPOXYALKENE OR A GAMMA, DELTA-EPOXYCYCLOALKENE IN LIQUID PHASE WITH SOLUTION OF CATALYTIC AMOUNT OF ORGANOTIN (IV) OR ORGANOANTIMONY COMPOUND IN INERT ORGANIC SOLVENT AND QUATERNARY ORGANIC ONIUM IODIDE | EASTMAN CHEMICAL COMPANY | 2001-03-13 | — | — | US | disclosed |
| US-6201139-B1 | CONTACTING A GAMMA, DELTA-EPOXYALKENE OR A GAMMA, DELTA-EPOXYCYCLOALKENE IN THE LIQUID PHASE WITH A SOLUTION OF A CATALYTIC AMOUNT OF AN ORGANOTIN (IV) COMPOUND OR ORGANOANTIMONY COMPOUND IN AN INERT, ORGANIC SOLVENT | EASTMAN CHEMICAL COMPANY | 2001-03-13 | — | — | US | disclosed |
| EP-0691334-B1 | Process for the preparation of 2,5-dihydrofuran | BASF AG (DE) | 1997-12-03 | — | — | EP | disclosed |
| US-5126406-A | Polyoxazolidones of good heat resistance and impact strength | NIPPON PAINT CO., LTD. (JP) | 1992-06-30 | — | — | US | disclosed |
| US-5117044-A | Unsaturated ester | NIPPON PAINT CO., LTD. (JP) | 1992-05-26 | — | — | US | disclosed |
| US-5102951-A | Curable compound | NIPPON PAINT CO., LTD. (JP) | 1992-04-07 | — | — | US | disclosed |
| US-5082956-A | Quaternary onium iodide catalyst | EASTMAN KODAK COMPANY (US) | 1992-01-21 | — | — | US | disclosed |
| US-5081183-A | Active hydrogen compound reacted with oxalic acid diester or acyl halide, curing agents | NIPPON PAINT CO., LTD. (JP) | 1992-01-14 | — | — | 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 |
| EP-0444956-A2 | Thermosetting resin composition and article obtained therefrom | NIPPON PAINT CO., LTD. (JP) | 1991-09-04 | — | — | EP | disclosed |
| EP-0390305-A2 | Diester and keto-ester derivatives of polyhydroxy compounds and production thereof | NIPPON PAINT CO., LTD. (JP) | 1990-10-03 | — | — | EP | disclosed |
| EP-0378429-A2 | Polymerisable compound and polymer therefrom | NIPPON PAINT CO., LTD. (JP) | 1990-07-18 | — | — | EP | disclosed |
| US-4298499-A | Recovery of catalysts | UOP INC. (US) | 1981-11-03 | — | — | US | disclosed |