⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL24103206 | 0.78 | MEN1 (0.52) | — | |
| SCHEMBL5077055 | 0.69 | — | — | |
| SCHEMBL20195637 | 0.68 | — | — | |
| SCHEMBL29742575 | 0.67 | CHRM2 (0.37) | — | |
| SCHEMBL573582 | 0.67 | CHRM2 (0.37) | — | |
| SCHEMBL6520902 | 0.67 | TTR (0.35) | — | |
| SCHEMBL13330042 | 0.67 | — | — | |
| SCHEMBL28282646 | 0.65 | — | — | |
| SCHEMBL29023882 | 0.65 | — | — | |
| SCHEMBL28436926 | 0.65 | TTR (0.40) | — |
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 34 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115073408-A | Synthetic method of 2,3,4, 6-tetrabenzyl-D-glucopyranose | 江苏法安德医药科技有限公司 | 2022-09-20 | — | — | CN | claimed |
| CN-114163466-A | Rapid detection Cr3+Preparation method and application of rhodamine B boron cluster derivative ultraviolet probe | 江汉大学 | 2022-03-11 | — | — | CN | claimed |
| CN-111377822-A | Preparation method of vilanterol | 天津药业研究院有限公司 | 2020-07-07 | — | — | CN | claimed |
| US-20100010212-A1 | Processes for the preparation of (3R,4S)-4-((4-benzyloxy)phenyl)-1-(4-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-2-azetidinone, an intermediate for the synthesis of ezetimibe | KANSAL VINOD KUMAR | 2010-01-14 | — | — | US | claimed |
| US-20070259845-A1 | Processes for the preparation of (3R,4S)-4-((4-benzyloxy)phenyl)-1-(4-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)-2-azetidinone, an intermediate for the synthesis of ezetimibe | TEVA PHARMACEUTICALS USA, INC. | 2007-11-08 | — | — | US | claimed |
| CN-111377822-B | Preparation method of vilanaflo | 天津药业研究院股份有限公司 | 2023-09-08 | — | — | CN | disclosed |
| CN-115191019-B | Capacitor with a capacitor body | 太阳电子工业株式会社 | 2023-07-07 | — | — | CN | disclosed |
| CN-115073408-A | Synthetic method of 2,3,4, 6-tetrabenzyl-D-glucopyranose | 江苏法安德医药科技有限公司 | 2022-09-20 | — | — | CN | disclosed |
| CN-114163466-A | Rapid detection Cr3+Preparation method and application of rhodamine B boron cluster derivative ultraviolet probe | 江汉大学 | 2022-03-11 | — | — | CN | disclosed |
| CN-114163466-A | Rapid detection Cr3+Preparation method and application of rhodamine B boron cluster derivative ultraviolet probe | 江汉大学 | 2022-03-11 | — | — | CN | disclosed |
| EP-3732171-A1 | METHODS FOR PREPARING FUEL ADDITIVES | BP Oil International Limited (GB) | 2020-11-04 | — | — | EP | disclosed |
| EP-3732172-A1 | METHODS FOR PREPARING FUEL ADDITIVES | BP Oil International Limited (GB) | 2020-11-04 | — | — | EP | disclosed |
| WO-2007120824-A2 | PROCESSES FOR THE SYNTHESIS OF AZETIDINONE | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2007-10-25 | — | — | WO | disclosed |
| CN-1938342-A | Compound for optical material and method for producing the same | GEN ELECTRIC (US) | 2007-03-28 | — | — | CN | disclosed |
| WO-2007030721-A2 | PROCESSES FOR THE PREPARATION OF (3R,4S)-4-((4-BENZYLOXY)PHENYL)-1-(4-FLUOROPHENYL)-3-((S)-3-(4-FLUOROPHENYL)-3-HYDROXYPROPYL)-2-AZETIDINONE, AN INTERMEDIATE FOR THE SYNTHESIS OF EZETIMIBE | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2007-03-15 | — | — | WO | disclosed |
| CN-1545502-A | Process for the preparation of indole derivatives | �������⻯ѧƷ�ع�����˾ | 2004-11-10 | — | — | CN | disclosed |
| EP-0736509-B1 | Processes for preparing optically active alcohols and optically active amines | SUMITOMO CHEMICAL CO (JP) | 2001-11-14 | — | — | EP | disclosed |
| US-6025531-A | REACTING A PROCHIRAL KETONE WITH A MIXTURE BORON-CONTAINING COMPOUNDS HAVING A BORANE REACTION PRODUCT FROM OPTICALLY ACTIVE BETA-AMINOALCOHOL AND A BORON HYDRIDE OR A METAL BOROHYDRIDE, AND AN OPTICALLY ACTIVE OXAZABOROLIDINE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2000-02-15 | — | — | US | disclosed |
| US-5801280-A | Processes for preparing optically active alcohols and optically active amines | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1998-09-01 | — | — | US | disclosed |
| EP-0736509-A2 | Processes for preparing optically active alcohols and optically active amines | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1996-10-09 | — | — | EP | disclosed |