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307:. It crystallizes as needles that melt at 170−171 °C. It was isolated in 1997 by S. Begum and others.
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Sabira Begum, Mansour Ahmed, Bina S. Siddiqui, Abdullah Khan, Zafar S. Saify, and
Mohammed Arif (1997),
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Triterpenes, a sterol and a monocyclic alcohol from
Momordica charantia.
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Except where otherwise noted, data are given for materials in their
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CC/C=C/C(C)(O)OC1(2CC3((2(CCC1=O)C)CC43(CC5(4((CC5)C)C)C)C)C)C
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Phytochemistry, volume 44, issue 7, pages 1313-1320
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284:, found in the fresh fruit of the
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228:(at 25 °C , 100 kPa).
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295:The compound is soluble in
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250:is a chemical compound, a
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40:(4β)-23-oxy]-ursan-3-one
290:Momordica charantia
218: g·mol
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446:Biochemistry stubs
232:Infobox references
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240:Chemical compound
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124:CompTox Dashboard
87:Interactive image
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248:24--ursan-3-one
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17:Momordicilin
391:expanding it
383:biochemistry
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327:Momordicinin
317:Momordicin I
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286:bitter melon
252:triterpenoid
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244:Momordicilin
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46:Identifiers
436:Triterpenes
303:but not in
176:Properties
63:189156-40-9
430:Categories
343:References
332:Momordenol
301:chloroform
211:Molar mass
74:3D model (
53:CAS Number
37:IUPAC name
112:102066427
337:Momordol
311:See also
441:Ketones
216:540.873
99:PubChem
305:petrol
160:SMILES
31:Names
381:This
76:JSmol
387:stub
299:and
292:).
246:or
129:EPA
102:CID
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351:^
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274:O
265:H
256:C
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201:O
195:H
189:C
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