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InChI=1S/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30+/m0/s1
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InChI=1/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30+/m0/s1
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Kang, Soo Yeon; Schini-Kerth, Valérie B.; Kim, Nak Doo (1995). "Ginsenosides of the protopanaxatriol group cause endothelium-dependent relaxation in the rat aorta".
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Except where otherwise noted, data are given for materials in their
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O41(CC1(2((3(C)((O)C2)C(C)(C)(O)CC3)C4)C)C)(O)(C)CC\C=C(/C)C
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98:)-1--3a,3b,6,6,9a-pentamethylhexadecahydro-1
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260:Key: SHCBCKBYTHZQGZ-DLHMIPLTSA-N
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397:) is an organic compound that is an
102:-cyclopentaphenanthrene-5,7,11-triol
270:Key: SHCBCKBYTHZQGZ-DLHMIPLTBT
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47:)-Dammar-24-ene-3β,6α,12β,20-tetrol
525:. You can help Knowledge (XXG) by
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352:(at 25 °C , 100 kPa).
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517:This article about an
54:Systematic IUPAC name
16:Ginseng plant extract
434:Panax pseudoginseng
342: g·mol
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413:-type tetracyclic
407:steroid glycosides
379:Infobox references
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478:(19): 1577–1586.
387:Chemical compound
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150:Interactive image
20:Protopanaxatriol
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109:Identifiers
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577:Triterpenes
446:Panaxatriol
430:notoginseng
300:Properties
566:Categories
457:References
418:sapogenins
415:triterpene
409:. It is a
335:Molar mass
235:ZMK19P3WMP
161:ChemSpider
137:3D model (
126:34080-08-5
116:CAS Number
40:IUPAC name
428:) and in
420:found in
411:dammarane
587:Steroids
440:See also
399:aglycone
582:Tetrols
519:alcohol
492:7723586
422:ginseng
372:what is
370: (
340:476.742
215:9847853
202:PubChem
170:8023566
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367:verify
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284:SMILES
190:C20716
34:Names
521:is a
249:InChI
139:JSmol
523:stub
488:PMID
226:UNII
181:KEGG
94:,11a
480:doi
436:).
401:of
395:PPT
205:CID
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