⚠ 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 | |
|---|---|---|---|---|
| Urea SCHEMBL497856 | 1.00 | — | — | |
| Bicarbonate SCHEMBL7761714 | 0.85 | ALDH1A1 (0.46) | — | |
| Bicarbonate SCHEMBL702706 | 0.85 | — | — | |
| Bicarbonate SCHEMBL28408643 | 0.85 | — | — | |
| Bicarbonate SCHEMBL28403504 | 0.85 | — | — | |
| Acetic Acid SCHEMBL27333843 | 0.83 | ALDH1A1 (0.38) | — | |
| Acetic Acid SCHEMBL11748243 | 0.82 | — | — | |
| Methyl Alcohol SCHEMBL9696132 | 0.81 | — | — | |
| Hydrazine SCHEMBL28228235 | 0.81 | — | — | |
| SCHEMBL25429748 | 0.80 | TRPA1 (0.39) | — |
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 76 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115637020-A | Hyperbranched epoxy resin thermosetting resin composition and application thereof | 复旦大学 | 2023-01-24 | — | — | CN | claimed |
| WO-2022262768-A1 | HYBUTIMIBE INTERMEDIATE AND PREPARATION METHOD THEREFOR | 浙江海正药业股份有限公司 | 2022-12-22 | — | — | WO | claimed |
| CN-113908664-A | Adsorbent for propylene-propane separation, preparation method thereof and propylene-propane separation method | 中国石油大学(北京) | 2022-01-11 | — | — | CN | claimed |
| WO-2021103256-A1 | CONTINUOUS SYNTHESIS METHOD FOR 2-CHLOROPYRIMIDINE-4-FORMIC ACID COMPOUND | 天津凯莱英制药有限公司 | 2021-06-03 | — | — | WO | claimed |
| EP-3060573-B1 | TETRAPEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME | KANEKA CORP (JP) | 2019-07-17 | — | — | EP | claimed |
| US-9982014-B2 | Tetrapeptide compound and method for producing same | KANEKA CORPORATION (JP) | 2018-05-29 | — | — | US | claimed |
| US-20160264623-A1 | TETRAPEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME | STEALTH BIOTHERAPEUTICS INC. | 2016-09-15 | — | — | US | claimed |
| EP-3060573-A1 | TETRAPEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME | Kaneka Corporation (JP) | 2016-08-31 | — | — | EP | claimed |
| WO-2016040500-A1 | IONIC LIQUID BIOPROCESSING | HYRAX ENERGY, INC. (US) | 2016-03-17 | — | — | WO | claimed |
| WO-2015060462-A1 | TETRAPEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME | KANEKA CORPORATION (JP) | 2015-04-30 | — | — | WO | claimed |
| EP-0655454-B1 | Process for preparing 2,2-difluoroketene silyl acetals and alpha,alpha-difluoro-beta-silyloxy-1,3-dioxolane-4-propanoic acid esters | LILLY CO ELI (US) | 2001-08-16 | — | — | EP | claimed |
| EP-0655454-A1 | Process for preparing 2,2-difluoroketene silyl acetals and a,a-difluoro-b-silyloxy-1,3-dioxolane-4-propanoic acid esters | ELI LILLY AND COMPANY (US) | 1995-05-31 | — | — | EP | claimed |
| CN-117776871-A | Method for synthesizing 2, 4-pentadiene-1-alcohol by using C5 sugar alcohol | 南京工业大学 | 2024-03-29 | — | — | CN | disclosed |
| EP-4223736-A1 | PRODUCTION METHOD FOR FLUORINATED ORGANIC COMPOUND | Daikin Industries, Ltd. (JP) | 2023-08-09 | — | — | EP | disclosed |
| US-20230242468-A1 | PRODUCTION METHOD FOR FLUORINATED ORGANIC COMPOUND | DAIKIN INDUSTRIES, LTD. (JP) | 2023-08-03 | — | — | US | disclosed |
| CN-116143601-A | Synthesis method of cyclopropyl methyl ketone | 如东众意化工有限公司 | 2023-05-23 | — | — | CN | disclosed |
| EP-0346795-A2 | Process for the production of polyarylene sulfides | IDEMITSU PETROCHEMICAL CO. LTD. (JP) | 1989-12-20 | — | — | EP | disclosed |
| US-4605713-A | Process for the production of polyarylene sulphides with functional end groups | BAYER AKTIENGESELLSCHAFT (DE) | 1986-08-12 | — | — | US | disclosed |
| US-4605732-A | Process for the production of polyarylene sulphides with functional end groups | BAYER AKTIENGESELLSCHAFT (DE) | 1986-08-12 | — | — | US | disclosed |
| US-4525579-A | Process for the production of optionally branched polyarylene sulphides with polyhalogenated polyaromatic compound | BAYER AKTIENGESELLSCHAFT (DE) | 1985-06-25 | — | — | US | disclosed |