⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL29798 | 1.00 | — | — | |
| SCHEMBL709962 | 1.00 | — | — | |
| Glycerin SCHEMBL1619849 | 0.96 | THRB (0.93) | — | |
| Water SCHEMBL1268536 | 0.96 | — | — | |
| Potassium SCHEMBL31010587 | 0.96 | — | — | |
| Ethane SCHEMBL940430 | 0.93 | — | — | |
| SCHEMBL4602198 | 0.93 | THRB (0.87) | — | |
| SCHEMBL29263423 | 0.90 | — | — | |
| Alcohol SCHEMBL21623931 | 0.90 | THRB (0.81) | — | |
| Boric Acid SCHEMBL28729468 | 0.90 | THRB (0.81) | — |
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 404 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119954752-A | Preparation method of (S) - (+) -3-hydroxytetrahydrofuran | 昊禾生物科技(常州)有限公司 | 2025-05-09 | — | — | CN | claimed |
| EP-4087931-B1 | NOVEL TLR9 AGONISTS | SBI BIOTECH CO LTD (JP) | 2024-12-25 | — | — | EP | claimed |
| CN-113337546-B | Preparation method of (S) -1,2, 4-butanetriol | 上海启讯医药科技有限公司 | 2023-09-12 | — | — | CN | claimed |
| US-20220402833-A1 | Nutritional Compositions for Plants and Soils | ENVIROKURE, INCORPORATED (US) | 2022-12-22 | — | — | US | claimed |
| EP-4087931-A1 | NOVEL TLR9 AGONISTS | SBI Biotech Co., Ltd. (JP) | 2022-11-16 | — | — | EP | claimed |
| CN-111056918-B | Preparation method of (S) -1,2,4-butanetriol | 上海科利生物医药有限公司 | 2022-10-14 | — | — | CN | claimed |
| CN-114981436-A | Novel TLR9 agonists | SBI生物技术有限公司 | 2022-08-30 | — | — | CN | claimed |
| CN-112941114-B | Method for synthesizing (S) -1,2, 4-butanetriol by enzyme method | 江苏惠利生物科技有限公司 | 2022-05-17 | — | — | CN | claimed |
| CN-114195743-A | Synthesis method of (S) -3-hydroxytetrahydrofuran | 厦门弘毅元素科技有限公司 | 2022-03-18 | — | — | CN | claimed |
| CN-113337546-A | Preparation method of (S) -1,2, 4-butanetriol | 上海启讯医药科技有限公司 | 2021-09-03 | — | — | CN | claimed |
| US-6376683-B1 | ESTERIFICATION OF MALIC ACID WITH ALCOHOL; REDUCTION; CYCLIZATION | COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) | 2002-04-23 | — | — | US | claimed |
| EP-0923516-B1 | PROCESS FOR THE PREPARATION OF BUTANE TRIOLS | AVECIA LTD (GB) | 2001-11-07 | — | — | EP | claimed |
| EP-0879893-B1 | Method of producing optically active 1,2,4-butanetriol | DAICEL CHEM (JP) | 2001-09-26 | — | — | EP | claimed |
| WO-2001046135-A1 | SYNTHESIS OF CHIRAL 2-AZETIDINEMETHANOL COMPOUNDS | ABBOTT LABORATORIES (US) | 2001-06-28 | — | — | WO | claimed |
| JP-2000516947-A | — | — | 2000-12-19 | — | — | JP | claimed |
| US-6124474-A | Synthesis of chiral 2-azetidinemethanol compounds | ABBOTT LABORATORIES (US) | 2000-09-26 | — | — | US | claimed |
| US-6027926-A | SIMPLE AND EFFICIENT METHOD BY CONTACTING MIXTURE OF ENANTIOMERS WITH MICROORGANISM OR A DISRUPTED, ACETONE-TREATED, OR LYOPHILIZED MICROORGANISM | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 2000-02-22 | — | — | US | claimed |
| EP-0923516-A1 | PROCESS FOR THE PREPARATION OF BUTANE TRIOLS | ZENECA LIMITED (GB) | 1999-06-23 | — | — | EP | claimed |
| EP-0879893-A1 | Method of producing optically active 1,2,4-butanetriol | DAICEL CHEMICAL INDUSTRIES, Ltd. (JP) | 1998-11-25 | — | — | EP | claimed |
| WO-1998008793-A1 | PROCESS FOR THE PREPARATION OF BUTANE TRIOLS | ZENECA LIMITED (GB) | 1998-03-05 | — | — | WO | claimed |