⚠ 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 | |
|---|---|---|---|---|
| Methylsulfanylmethane SCHEMBL1549136 | 0.71 | — | — | |
| SCHEMBL804643 | 0.59 | — | — | |
| SCHEMBL11056207 | 0.59 | — | — | |
| SCHEMBL17049775 | 0.56 | — | — | |
| SCHEMBL21449920 | 0.56 | — | — | |
| SCHEMBL17326365 | 0.56 | — | — | |
| SCHEMBL19278168 | 0.56 | — | — | |
| SCHEMBL1546497 | 0.54 | — | — | |
| SCHEMBL14193444 | 0.54 | — | — | |
| Methylsulfanylmethane SCHEMBL7985077 | 0.54 | — | — |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20240229131-A1 | TRANSITION-METAL CATALYST COMPOSITIONS AND METHODS FOR SEQUENCING BY SYNTHESIS | ILLUMINA, INC. | 2024-07-11 | — | — | US | disclosed |
| US-20240218443-A1 | METHODS OF SEQUENCING USING 3' BLOCKED NUCLEOTIDES | ILLUMINA, INC. | 2024-07-04 | — | — | US | disclosed |
| US-20240209015-A1 | METHODS OF SEQUENCING USING 3' BLOCKED NUCLEOTIDES | ILLUMINA, INC. | 2024-06-27 | — | — | US | disclosed |
| WO-2024137774-A1 | PALLADIUM CATALYST COMPOSITIONS AND METHODS FOR SEQUENCING BY SYNTHESIS | ILLUMINA, INC. (US) | 2024-06-27 | — | — | WO | disclosed |
| WO-2024137765-A1 | TRANSITION-METAL CATALYST COMPOSITIONS AND METHODS FOR SEQUENCING BY SYNTHESIS | ILLUMINA, INC. (US) | 2024-06-27 | — | — | WO | disclosed |
| US-20240182963-A1 | METHODS OF SEQUENCING USING 3' BLOCKED NUCLEOTIDES | ILLUMINA, INC. | 2024-06-06 | — | — | US | disclosed |
| US-11008290-B2 | Halogenated quinoline derivatives as antimicrobial agents | UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) | 2021-05-18 | — | — | US | disclosed |
| US-10736966-B2 | Brush-poly (glycoamidoamine)-lipids and uses thereof | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2020-08-11 | — | — | US | disclosed |
| US-20180265475-A1 | HALOGENATED QUINOLINE DERIVATIVES AS ANTIMICROBIAL AGENTS | UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) | 2018-09-20 | — | — | US | disclosed |
| US-9840479-B2 | Polyamine-fatty acid derived lipidoids and uses thereof | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2017-12-12 | — | — | US | disclosed |
| EP-3164379-A1 | POLYAMINE-FATTY ACID DERIVED LIPIDOIDS AND USES THEREOF | Massachusetts Institute of Technology (US) | 2017-05-10 | — | — | EP | disclosed |
| WO-2017053696-A2 | HALOGENATED QUINOLINE DERIVATIVES AS ANTIMICROBIAL AGENTS | UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) | 2017-03-30 | — | — | WO | disclosed |
| US-20160067346-A1 | BRUSH-POLY (GLYCOAMIDOAMINE)-LIPIDS AND USES THEREOF | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2016-03-10 | — | — | US | disclosed |
| WO-2016025643-A1 | BRUSH-POLY(GLYCOAMIDOAMINE)-LIPIDS AND USES THEREOF | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2016-02-18 | — | — | WO | disclosed |
| WO-2016004202-A1 | POLYAMINE-FATTY ACID DERIVED LIPIDOIDS AND USES THEREOF | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2016-01-07 | — | — | WO | disclosed |
| US-20160002178-A1 | POLYAMINE-FATTY ACID DERIVED LIPIDOIDS AND USES THEREOF | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2016-01-07 | — | — | US | disclosed |
| WO-2015055576-A1 | PHOTOPOLYMER FORMULATION FOR PRODUCTION OF HOLOGRAPHIC MEDIA COMPRISING BORATES WITH LOW TG | BAYER MATERIALSCIENCE AG (DE) | 2015-04-23 | — | — | WO | disclosed |
| US-5220072-A | Reacting 2-ethylapopinene enantiomorph with haloborane-methyl sulfide complex | ALDRICH CHEMICAL CO., INC. (US) | 1993-06-15 | — | — | US | disclosed |
| US-5202502-A | Using b-halodiiso-2-ethylapopinocampheylborane as reducing agent | ALDRICH CHEMICAL COMPANY, INC. (US) | 1993-04-13 | — | — | US | disclosed |
| US-5159116-A | Reducing agents in the asymmetric reduction of ketones to optically active alcohols | ALDRICH CHEMICAL COMPANY, INC. (US) | 1992-10-27 | — | — | US | disclosed |