⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL11124019 | 1.00 | CYP1A2 (0.62) | — | |
| SCHEMBL10569491 | 1.00 | CYP1A2 (0.62) | — | |
| SCHEMBL10569484 | 1.00 | CYP1A2 (0.62) | — | |
| SCHEMBL997470 | 0.97 | CYP1A2 (0.59) | — | |
| SCHEMBL2048536 | 0.97 | — | — | |
| SCHEMBL8462718 | 0.97 | CYP1A2 (0.67) | — | |
| SCHEMBL6753110 | 0.97 | CYP1A2 (0.59) | — | |
| SCHEMBL1847927 | 0.97 | CYP1A2 (0.59) | — | |
| Bromide SCHEMBL9837977 | 0.97 | — | — | |
| SCHEMBL6749100 | 0.97 | CYP1A2 (0.59) | — |
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 689 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20240131040-A1 | COMPOSITIONS AND METHODS RELATED TO CANNABINOID ANIONS | Natural Extraction Systems, LLC (US) | 2024-04-25 | — | — | US | claimed |
| CN-117741007-A | Noni fruit maturity identification method | 中国热带农业科学院香料饮料研究所 | 2024-03-22 | — | — | CN | claimed |
| CN-116905020-A | Method for synthesizing 1, 3-fluoroamine product by electrochemical mode | 南京工业大学 | 2023-10-20 | — | — | CN | claimed |
| CN-116905005-A | Method for synthesizing 1, 3-oxyfluoride product by electrochemical mode | 南京工业大学 | 2023-10-20 | — | — | CN | claimed |
| CN-113372319-B | Amine group-containing delta-lactone compound and preparation method thereof | 东北师范大学 | 2023-09-05 | — | — | CN | claimed |
| US-20230089351-A1 | METHODS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES | Natural Extraction Systems, LLC (US) | 2023-03-23 | — | — | US | claimed |
| US-20230073802-A1 | COMPOSITIONS AND METHODS RELATED TO CANNABINOID ANIONS | Natural Extraction Systems, LLC (US) | 2023-03-09 | — | — | US | claimed |
| CN-111018827-B | Polysubstituted thiophene derivative and synthetic method thereof | 中国科学院大连化学物理研究所 | 2022-12-30 | — | — | CN | claimed |
| US-20220387351-A1 | Compositions and Methods Related to Organic Oxides | Natural Extraction Systems, LLC | 2022-12-08 | — | — | US | claimed |
| US-20220387376-A1 | Compositions Comprising Cannabinoid Molecules that are Dissolved in Water-Miscible Solvents | NATURAL EXTRACTION SYS LLC (US) | 2022-12-08 | — | — | US | claimed |
| CN-1037098-C | Pesticidal fluoroolefins | BRITISH TECH GROUP (GB) | 1998-01-21 | — | — | CN | claimed |
| EP-0798318-A2 | Process for controlling gas phase fluidized bed polymerization reactor | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) | 1997-10-01 | — | — | EP | claimed |
| US-5627242-A | REDUCING THE OFFGRADE MATERIAL OF ALPHA-OLEFIN POLYMERS PRODUCED DURING GRADE TRANSITION OR DURING STEADY STATE MANUFACTURE BY ADJUSTING THE SET POINT FOR MELT INDEX, REACTION TEMPERATURE AND PARTIAL PRESSURE | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) | 1997-05-06 | — | — | US | claimed |
| EP-0660815-B1 | PESTICIDAL FLUOROOLEFINS | BRITISH TECH GROUP (GB) | 1997-04-16 | — | — | EP | claimed |
| EP-0610819-B1 | Process for the preparation of acylcyclopropanes | BASF AG (DE) | 1996-08-21 | — | — | EP | claimed |
| EP-0660815-A1 | PESTICIDAL FLUOROOLEFINS. | BRITISH TECNOLOGY GROUP PLC (GB) | 1995-07-05 | — | — | EP | claimed |
| CN-1087895-A | Pesticidal fluoroolefins | BRITISH TECH GROUP (GB) | 1994-06-15 | — | — | CN | claimed |
| WO-1994006741-A1 | PESTICIDAL FLUOROOLEFINS | BRITISH TECHNOLOGY GROUP LIMITED (GB) | 1994-03-31 | — | — | WO | claimed |
| US-5200477-A | Having antiagglomerant inert particles with an organomodified polysiloxane present during the vapor phase polymerization to produce synthetic rubbers using a coordination catalyst | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) | 1993-04-06 | — | — | US | claimed |
| CN-85108725-A | The preparation method and the application thereof of the pyrroles's methyl-cyclopropyl-carbinol derivatives that replaces | — | 1986-05-10 | — | — | CN | claimed |