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 | 3/20 | 0.50 |
| ▸ | LMNA | P02545 | 5/20 | 0.50 |
| ▸ | TSHR | P16473 | 1/20 | 0.50 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.50 |
| ▸ | HPGD | P15428 | 3/20 | 0.42 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.42 |
| ▸ | CES2 | O00748 | 1/20 | 0.39 |
| ▸ | CES1 | P23141 | 1/20 | 0.39 |
| ▸ | NPC1 | O15118 | 3/20 | 0.38 |
| ▸ | RAB9A | P51151 | 3/20 | 0.38 |
| ▸ | MEN1 | O00255 | 2/20 | 0.38 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.38 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.38 |
| ▸ | MAPT | P10636 | 1/20 | 0.38 |
| ▸ | HKDC1 | Q2TB90 | 1/20 | 0.38 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.38 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.36 |
| ▸ | SMN1; SMN2 | Q16637 | 4/20 | 0.35 |
| ▸ | POLB | P06746 | 2/20 | 0.35 |
| ▸ | HTT | P42858 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL29404005 | 0.97 | ACHE (0.53) | LMNAACHETSHRALOX12HPGD | |
| Hydrochloric Acid SCHEMBL7058630 | 0.95 | ACHE (0.50) | LMNAACHETSHRALOX12HPGD | |
| Bromide SCHEMBL7063570 | 0.95 | ACHE (0.50) | LMNAACHETSHRALOX12HPGD | |
| Iodide SCHEMBL10656368 | 0.89 | ACHE (0.53) | LMNAACHETSHRALOX12TDP1 | |
| SCHEMBL7065118 | 0.88 | ACHE (0.43) | LMNAACHETSHRALOX12HPGD | |
| SCHEMBL11314306 | 0.88 | ACHE (0.43) | LMNAACHETSHRALOX12HPGD | |
| Iodide SCHEMBL9182282 | 0.86 | ACHE (0.50) | LMNAACHETSHRALOX12TDP1 | |
| Thiocyanic Acid SCHEMBL4447159 | 0.84 | ALDH1A1 (0.43) | LMNAACHETSHRALOX12HPGD | |
| SCHEMBL503495 | 0.84 | TSHR (0.40) | LMNAACHETSHRALOX12HPGD | |
| SCHEMBL7065117 | 0.84 | ACHE (0.40) | LMNAACHETSHRALOX12HPGD |
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.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1013633-B1 | Process for producing a diaryl carbonate | UBE INDUSTRIES (JP) | 2003-05-28 | — | — | EP | disclosed |
| EP-0832910-B1 | Process for producing a polycarbonate | UBE INDUSTRIES (JP) | 2002-06-26 | — | — | EP | disclosed |
| EP-0832872-B1 | Process for producing diaryl carbonate | UBE INDUSTRIES (JP) | 2002-01-30 | — | — | EP | disclosed |
| EP-0795539-B1 | Process for producing a diaryl carbonate | UBE INDUSTRIES (JP) | 2001-10-31 | — | — | EP | disclosed |
| EP-0834496-B1 | Preparation of diaryl carbonate | UBE INDUSTRIES (JP) | 2001-08-16 | — | — | EP | disclosed |
| EP-0834495-B1 | Process for preparing diaryl carbonate | UBE INDUSTRIES (JP) | 2000-12-27 | — | — | EP | disclosed |
| EP-1013633-A1 | Process for producing a diaryl carbonate | Ube Industries, Ltd. (JP) | 2000-06-28 | — | — | EP | disclosed |
| US-5922827-A | Process for producing a polycarbonate | UBE INDUSTRIES, LTD. (JP) | 1999-07-13 | — | — | US | disclosed |
| US-5892091-A | PHOSPHOROUS CATALYSTS AND HALOGEN ATOMS | UBE INDUSTRIES, LTD. (JP) | 1999-04-06 | — | — | US | disclosed |
| US-5892089-A | FROM DIARYL OXALATE IN LIQUID PHASE BY DECARBONYLATION USING ORGANIC PHOSHORUS COMPOUND CATALYST | UBE INDUSTRIES, LTD. (JP) | 1999-04-06 | — | — | US | disclosed |
| EP-0832910-A2 | Process for producing a polycarbonate | UBE INDUSTRIES, LTD. (JP) | 1998-04-01 | — | — | EP | disclosed |
| US-5731453-A | Process for producing a diaryl carbonate | UBE INDUSTRIES, LTD. (JP) | 1998-03-24 | — | — | US | disclosed |
| EP-0826658-A1 | Catalyst for decarbonylation reaction | UBE INDUSTRIES, LTD. (JP) | 1998-03-04 | — | — | EP | disclosed |
| EP-0795539-A1 | Process for producing a diaryl carbonate | UBE INDUSTRIES LIMITED (JP) | 1997-09-17 | — | — | EP | disclosed |
| US-5648510-A | DECARBONYLATION OF OXALATE | UBE INDUSTRIES, LTD. (JP) | 1997-07-15 | — | — | US | disclosed |
| EP-0737665-A1 | Process for preparation of diaryl carbonate | UBE INDUSTRIES, LTD. (JP) | 1996-10-16 | — | — | EP | disclosed |
| US-4511517-A | COBALT AND IRON SOURCE, IODIDE | RHONE-POULENC CHIMIE DE BASE (FR) | 1985-04-16 | — | — | US | disclosed |
| US-4500474-A | Carbonylation of methyl acetate | RHONE-POULENC CHIMIE DE BASE (FR) | 1985-02-19 | — | — | US | disclosed |
| US-4431835-A | USING A CATALYST COMPRISING COMPOUNDS OF RUTHENIUM, COBALT, CHROMIUM AND AN IODIDE PROMOTER | RHONE-POULENC INDUSTRIES (FR) | 1984-02-14 | — | — | US | disclosed |
| US-4430506-A | CATALYST SYSTEM OF RUTHENIUM, COBALT, VANDIUM AND IODINE CONTAINING PROMOTER | RHONE-POULENC INDUSTRIES (FR) | 1984-02-07 | — | — | US | disclosed |