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InChI=1S/C20H30O3/c1-18(2)9-4-10-19(3)15(18)7-11-20(13-23-20)16(19)6-5-14-8-12-22-17(14)21/h5,15-16H,4,6-13H2,1-3H3/b14-5+/t15-,16+,19-,20+/m0/s1
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Huang, Q.; Iwamoto, Y.; Aoki, S.; Tanaka, N.; Tajima, K.; Yamahara, J.; Takaishi, Y.; Yoshida, M.; Tomimatsu, T.; Tamai, Y. (1991).
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368:"Anti-5-hydroxytryptamine3 effect of galanolactone, diterpenoid isolated from ginger"
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Except where otherwise noted, data are given for materials in their
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338:extracts of ginger, and appears to be an
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218:O=C/1OCCC\1=C\C42((C(CCC2)(C)C)CC43OC3)C
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372:Chemical & Pharmaceutical Bulletin
197:Key: MBPTXJNHCBXMBP-SDIIOJARSA-N
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45:)-3-{2--1-yl]ethylidene}oxolan-2-one
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282:(at 25 °C , 100 kPa).
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261:318.45 g/mol
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330:first isolated from
37:Preferred IUPAC name
334:. It is present in
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385:10.1248/cpb.39.397
309:Infobox references
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317:Chemical compound
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93:Interactive image
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52:Identifiers
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325:diterpenoid
269:in acetone
227:Properties
69:115753-79-2
419:Diterpenes
408:Categories
353:References
340:antagonist
267:Solubility
257:Molar mass
172:4FX4852TYQ
104:ChemSpider
80:3D model (
59:CAS Number
414:Furanones
347:receptors
429:Epoxides
424:Decalins
272:Soluble
152:11141699
394:2054863
336:acetone
328:lactone
302:what is
300: (
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139:PubChem
113:9316811
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332:ginger
297:verify
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211:SMILES
31:Names
344:5-HT3
323:is a
186:InChI
82:JSmol
390:PMID
163:UNII
124:MeSH
380:doi
342:at
142:CID
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292:N
249:3
247:O
243:H
239:C
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43:E
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