Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
The experimentally established mechanism targets of Formaldehyde. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| Formaldehyde SCHEMBL28170357 | 1.00 | — | — | |
| Formaldehyde SCHEMBL29620086 | 0.89 | — | — | |
| Formaldehyde SCHEMBL8330944 | 0.87 | — | — | |
| Formaldehyde SCHEMBL268 | 0.87 | — | — | |
| Formaldehyde SCHEMBL1347887 | 0.87 | — | — | |
| Formaldehyde SCHEMBL13582711 | 0.87 | — | — | |
| Formaldehyde SCHEMBL6977718 | 0.87 | — | — | |
| Formaldehyde SCHEMBL12190180 | 0.87 | — | — | |
| Formaldehyde SCHEMBL3907789 | 0.87 | — | — | |
| Formaldehyde SCHEMBL25319009 | 0.75 | — | — |
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 37 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120137274-A | Rubber with high performance, low rolling resistance and thermal oxidative aging resistance and preparation method thereof | 四川大学 | 2025-06-13 | — | — | CN | claimed |
| CN-116217392-A | Synthesis method of loxoprofen sodium key intermediate 2- (4-halomethylphenyl) propionate | 厦门医学院 | 2023-06-06 | — | — | CN | claimed |
| CN-114144408-A | Process and intermediates for large scale preparation of 2,4, 6-trifluoro-N- [6- (1-methyl-piperidine-4-carbonyl) -pyridin-2-yl ] -benzamide hemisuccinate and preparation of 2,4, 6-trifluoro-N- [6- (1-methyl-piperidine-4-carbonyl) -pyridin-2-yl ] -benzamide acetate | 伊莱利利公司 | 2022-03-04 | — | — | CN | claimed |
| US-12503557-B2 | Thermoplastic elastomer composition, joint member, and method for producing the same | MCPP INNOVATION LLC (JP) | 2025-12-23 | — | — | US | disclosed |
| CN-117717555-A | Soluble halofuginone anticoccidial composition | 重庆医药高等专科学校 | 2024-03-19 | — | — | CN | disclosed |
| EP-4219619-A1 | THERMOPLASTIC ELASTOMER COMPOSITION AND COMPOSITE MOLDED OBJECT | MCPP Innovation LLC (JP) | 2023-08-02 | — | — | EP | disclosed |
| US-20230220192-A1 | Thermoplastic Elastomer Composition and Composite Molded Body | MCPP INNOVATION LLC (JP) | 2023-07-13 | — | — | US | disclosed |
| CN-116217392-A | Synthesis method of loxoprofen sodium key intermediate 2- (4-halomethylphenyl) propionate | 厦门医学院 | 2023-06-06 | — | — | CN | disclosed |
| CN-113573904-B | Thermoplastic elastomer composition and molded article thereof | 三井化学株式会社 | 2023-04-18 | — | — | CN | disclosed |
| EP-4023705-A1 | THERMOPLASTIC ELASTOMER COMPOSITION, BONDING MEMBER AND METHOD FOR PRODUCING SAME | MCPP Innovation LLC (JP) | 2022-07-06 | — | — | EP | disclosed |
| US-20220177654-A1 | Thermoplastic Elastomer Composition, Joint Member, and Method for Producing the Same | MCPP INNOVATION LLC (JP) | 2022-06-09 | — | — | US | disclosed |
| CN-101287696-A | A process to enrich a carboxylic acid composition | EASTMAN CHEM CO (US) | 2008-10-15 | — | — | CN | disclosed |
| CN-101248035-A | An enriched terephthalic acid composition | EASTMAN CHEM CO (US) | 2008-08-20 | — | — | CN | disclosed |
| CN-101189207-A | A process to produce an enriched composition through the use of a catalyst removal zone and an enrichment zone | EASTMAN CHEM CO (US) | 2008-05-28 | — | — | CN | disclosed |
| CN-101184719-A | An enrichment process using compounds useful in a polyester process | EASTMAN CHEM CO (US) | 2008-05-21 | — | — | CN | disclosed |
| CN-101180253-A | Process to produce an enriched composition | EASTMAN CHEM CO (US) | 2008-05-14 | — | — | CN | disclosed |
| CN-101180254-A | Process to produce a post catalyst removal composition | EASTMAN CHEM CO (US) | 2008-05-14 | — | — | CN | disclosed |
| CN-101175710-A | An enriched isophthalic acid composition | EASTMAN CHEM CO (US) | 2008-05-07 | — | — | CN | disclosed |
| US-5318666-A | Forming n-p junction; dry reactive etching to form via | TEXAS INSTRUMENTS INCORPORATED (US) | 1994-06-07 | — | — | US | disclosed |
| CN-85101892-A | Process for preparing novel 1, 5-benzothiazepine derivatives | — | 1987-01-17 | — | — | CN | disclosed |