⚠ 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 | |
|---|---|---|---|---|
| Diethyl Sulfide SCHEMBL1327 | 0.94 | — | — | |
| Diethyl Sulfide SCHEMBL11391850 | 0.94 | — | — | |
| Diethyl Sulfide SCHEMBL5092086 | 0.94 | TSHR (0.33) | — | |
| Diethyl Sulfide SCHEMBL15059287 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL8074340 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL25414913 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL9743857 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL1422174 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL869475 | 0.89 | — | — | |
| Diethyl Sulfide SCHEMBL10939306 | 0.89 | — | — |
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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117004663-A | Method for synthesizing (R) -4-propyldihydrofuran-2 (3 hydrogen) -ketone | 上海颐碳化学科技有限公司 | 2023-11-07 | — | — | CN | claimed |
| CN-117004663-A | Method for synthesizing (R) -4-propyldihydrofuran-2 (3 hydrogen) -ketone | 上海颐碳化学科技有限公司 | 2023-11-07 | — | — | CN | disclosed |
| EP-2414350-A1 | HEPATITIS C VIRUS INHIBITORS | Bristol-Myers Squibb Company (US) | 2012-02-08 | — | — | EP | disclosed |
| EP-2062856-B1 | Preparation Of MnB12H12 | ROHM & HAAS (US) | 2011-03-16 | — | — | EP | disclosed |
| WO-2010117635-A1 | HEPATITIS C VIRUS INHIBITORS | BRISTOL-MYERS SQUIBB COMPANY (US) | 2010-10-14 | — | — | WO | disclosed |
| US-7732456-B2 | Pyridone derivative | BANYU PHARMACEUTICAL CO., LTD. (JP) | 2010-06-08 | — | — | US | disclosed |
| US-7563934-B2 | Preparation of MnB12H12 | ROHN AND HAAS COMPANY (US) | 2009-07-21 | — | — | US | disclosed |
| EP-2062856-A1 | Preparation Of MnB12H12 | Rohm and Haas Company (US) | 2009-05-27 | — | — | EP | disclosed |
| US-20090118526-A1 | Where M is a metal or ammonium cation and n is one or two by combining a metal borohydride and XBH3; wherein X is an amine containing at least one aryl group, aralkyl group or branched alkyl group, a phosphine having three aryl, aralkyl or branched alkyl groups or tetrahydrofuran | VERTELLUS PERFORMANCE CHEMICALS LLC | 2009-05-07 | — | — | US | disclosed |
| EP-1930325-A1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE PIPERAZINE COMPOUND | Sumitomo Chemical Company, Limited (JP) | 2008-06-11 | — | — | EP | disclosed |
| CN-1302116-C | Process for preparing enantiomers of (1R, 4S) -or (1S, 4R) -1-amino-4- (hydroxymethyl) -2-cyclopentene derivatives | LONZE AG (CH) | 2007-02-28 | — | — | CN | disclosed |
| CN-1827591-A | Process for preparing racemic or optically active 4- (hydroxymethyl) -2-cyclopentene derivatives | LONZA AG (CH) | 2006-09-06 | — | — | CN | disclosed |
| CN-1515673-A | Process for preparing enantiomers of (1R, 4S) -or (1S, 4R) -1-amino-4- (hydroxymethyl) -2-cyclopentene derivatives | ��¡���ӹɷ�����˾ | 2004-07-28 | — | — | CN | disclosed |
| CN-1115343-C | Process for the preparation of (1S,4R) -or (1R,4S) -4- (2-amino-6-chloro-9H-purin-9-yl) -2-cyclopentene-1-methanol or salts thereof | LONZA AG (CH) | 2003-07-23 | — | — | CN | disclosed |
| US-6262295-B1 | REACTING CYCLOPENTENE-4-CARBOXYLIC ACID WITH AN ACYL HALIDE | LONZA A.G. (CH) | 2001-07-17 | — | — | US | disclosed |
| US-6252112-B1 | MIBCROBIAL HYDROLYSIS OF THE TITLE COMPOUND DERIVATIVE USING ENZYME HAVING N-ACETYLAMINO-ALCOHOL HYDROLASE OR PENICILLIN G ACYLASE ACTIVITY WITH SUBSEQUENT ACYLATION | LONZA A.G., (CH) | 2001-06-26 | — | — | US | disclosed |
| US-6156893-A | Process for the preparation of (1S,4R)- or (1R,4S)- 4-(2-amino-6-chloro-9H-purin-9-yl)-2-cyclopentene-1-methanol | LONZA A.G. (CH) | 2000-12-05 | — | — | US | disclosed |
| US-6137007-A | CHEMICAL INTERMEDIATES FOR NUCLEOSIDE, 4-2-(AMINO-6-CHLORO-9H-PURIN-9-YL)-2-CYCLOPENTENE-1-METHANOL, WHICH IS AN INTERMEDIATE FOR 6-(CYCLOPROPYLAMINO)-DERIVATIVE | LONZA AG (CH) | 2000-10-24 | — | — | US | disclosed |
| CN-1201794-A | Process for the preparation of (1S,4R) -or (1R,4S) -4- (2-amino-6-chloro-9H-purin-9-yl) -2-cyclopentene-1-methanol or salts thereof | LONZA AG (CH) | 1998-12-16 | — | — | CN | disclosed |
| EP-0160258-B1 | (6,11-DIHYDRO-11-OXODIBENZ(BM,E)OXEPINYL)PENTANOLS, A PROCESS AND INTERMEDIATES FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1989-09-27 | — | — | EP | disclosed |