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.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Iodide SCHEMBL11661856 | 1.00 | — | — | |
| Fluoride SCHEMBL4297835 | 0.82 | — | — | |
| SCHEMBL7717809 | 0.71 | — | — | |
| Iodide SCHEMBL21886 | 0.71 | — | — | |
| SCHEMBL8088010 | 0.71 | — | — | |
| Iodide SCHEMBL6053672 | 0.71 | — | — | |
| SCHEMBL8027947 | 0.71 | — | — | |
| Iodide SCHEMBL2757576 | 0.71 | — | — | |
| Iodide SCHEMBL5037302 | 0.71 | — | — | |
| SCHEMBL8860959 | 0.71 | — | — |
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 692 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250349837-A1 | POSITIVE ELECTRODE ACTIVE MATERIAL, PREPARATION METHOD THEREOF, POSITIVE ELECTRODE PLATE, SECONDARY BATTERY, AND ELECTRIC APPARATUS | CONTEMPORARY AMPEREX TECHNOLOGY CO LTD (CN) | 2025-11-13 | — | — | US | claimed |
| EP-4641668-A1 | POSITIVE ELECTRODE ACTIVE MATERIAL AND PREPARATION METHOD THEREFOR, POSITIVE ELECTRODE SHEET, SECONDARY BATTERY, AND ELECTRIC DEVICE | Contemporary Amperex Technology Co., Limited (CN) | 2025-10-29 | — | — | EP | claimed |
| CN-119552183-B | Narrow emission compound based on spirobifluorene and electroluminescent device prepared from narrow emission compound | 中国科学院宁波材料技术与工程研究所 | 2025-06-17 | — | — | CN | claimed |
| CN-119895589-A | Positive electrode active material, preparation method thereof, positive electrode plate, secondary battery and electricity utilization device | 宁德时代新能源科技股份有限公司 | 2025-04-25 | — | — | CN | claimed |
| CN-115172669-B | Battery silicon negative electrode, preparation method, sulfide all-solid-state lithium battery and application | 高能时代(珠海)新能源科技有限公司 | 2025-04-11 | — | — | CN | claimed |
| WO-2025063847-A1 | HARD COATINGS FROM METAL BORIDE NANOCRYSTALS INK | RIJKSUNIVERSITEIT GRONINGEN (NL) | 2025-03-27 | — | — | WO | claimed |
| CN-119552183-A | Narrow emission compound based on spirobifluorene and electroluminescent device prepared from narrow emission compound | 中国科学院宁波材料技术与工程研究所 | 2025-03-04 | — | — | CN | claimed |
| WO-2024260368-A1 | BENZOFURAN DERIVATIVE AND PREPARATION METHOD FOR BENZOFURAN DERIVATIVE INTERMEDIATE | 江苏恒瑞医药股份有限公司 | 2024-12-26 | — | — | WO | claimed |
| WO-2024234371-A1 | POSITIVE ELECTRODE ACTIVE MATERIAL AND PREPARATION METHOD THEREFOR, POSITIVE ELECTRODE SHEET, SECONDARY BATTERY, AND ELECTRIC DEVICE | 宁德时代新能源科技股份有限公司 | 2024-11-21 | — | — | WO | claimed |
| CN-118045591-A | Preparation method, product and application of BN coated Ni catalyst | 浙江大学 | 2024-05-17 | — | — | CN | claimed |
| CN-1097429-A | Poly-dehydration aspartic acid and its biodegradable hydrolysate | RHONE POULENC CHIMIE (FR) | 1995-01-18 | — | — | CN | claimed |
| CN-1074378-A | Radiophotography is with contrast agent and contrast compositions and utilize the radiological imaging method of this type of medicament | GUERBET SA (FR) | 1993-07-21 | — | — | CN | claimed |
| EP-0342843-B1 | PROCESS FOR PREPARING RACEMIC DIHALOVINYLCYCLOPROPANE CARBOXYLIC ACID HALIDES | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-03-03 | — | — | EP | claimed |
| EP-0483555-A1 | An intrinsic arrangement for power stabilization in a thermal nuclear reactor | ANSALDO S.p.A. (IT) | 1992-05-06 | — | — | EP | claimed |
| US-5041670-A | Preparation of n-aryl amines from isocyanates | DREXEL UNIVERSITY (US) | 1991-08-20 | — | — | US | claimed |
| US-4962233-A | Process for preparing racemic dihalovinylcyclopropane carboxylic acid halides | SUMITOMO CHEMICAL CO., LTD. (JP) | 1990-10-09 | — | — | US | claimed |
| EP-0342843-A1 | Process for preparing racemic dihalovinylcyclopropane carboxylic acid halides | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-11-23 | — | — | EP | claimed |
| US-4659808-A | CATALYTIC REACTION WITH A KETONE | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1987-04-21 | — | — | US | claimed |
| EP-0138436-A2 | Process for producing ketals of 2-Ketogulonic acid or its esters | Takeda Chemical Industries, Ltd. (JP) | 1985-04-24 | — | — | EP | claimed |
| US-4024425-A | Metal halide lamps | TOKYO SHIBAURA ELECTRIC CO., LTD. (JA) | 1977-05-17 | — | — | US | claimed |