Acevaltrate
{{Chembox
| ImageFile = Acevaltrate.svg
| ImageSize = 200px
| ImageAlt =
| PIN = (1S,2′R,6S,7aS)-4-[(Acetyloxy)methyl]-1-[(3-methylbutanoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2′-oxiran]-6-yl 3-(acetyloxy)-3-methylbutanoate
| OtherNames = Acetoxyvaltrate; Acetovaltrate
|Section1={{Chembox Identifiers
| CASNo = 25161-41-5
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = S9MFK45GY9
| PubChem = 65717
| EINECS = 246-685-1
| ChemSpiderID = 59141
| ChEMBL = 563350
| SMILES = CC(C)CC(=O)O[C@H]1[C@H]2C(=C[C@@H]([C@]23CO3)OC(=O)CC(C)(C)OC(=O)C)C(=CO1)COC(=O)C
| InChI = 1/C24H32O10/c1-13(2)7-19(27)33-22-21-17(16(11-30-22)10-29-14(3)25)8-18(24(21)12-31-24)32-20(28)9-23(5,6)34-15(4)26/h8,11,13,18,21-22H,7,9-10,12H2,1-6H3/t18-,21+,22-,24+/m0/s1
| InChIKey = FWKBQAVMKVZEOT-STCFVSJZBV
| StdInChI = 1S/C24H32O10/c1-13(2)7-19(27)33-22-21-17(16(11-30-22)10-29-14(3)25)8-18(24(21)12-31-24)32-20(28)9-23(5,6)34-15(4)26/h8,11,13,18,21-22H,7,9-10,12H2,1-6H3/t18-,21+,22-,24+/m0/s1
| StdInChIKey = FWKBQAVMKVZEOT-STCFVSJZSA-N}}
|Section2={{Chembox Properties
| C=24 | H=32 | O=10
| Appearance =
| Density =
| MeltingPtC = 80-81
| BoilingPt =
| Solubility = }}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt = }}
}}
Acevaltrate is an iridoid isolated from Valeriana glechomifolia.{{cite journal|pmid=21567360|year=2011|last1=Bettero|first1=GM|last2=Salles|first2=L|last3=Rosário Figueira|first3=RM|last4=Poser|first4=Gv|last5=Rates|first5=SM|last6=Noël|first6=F|last7=Quintas|first7=LE|title=In vitro effect of valepotriates isolated from Valeriana glechomifolia on rat P-type ATPases|volume=77|issue=15|pages=1702–6|doi=10.1055/s-0030-1271084|journal=Planta Medica|s2cid=260284677 }}
References
{{Reflist}}
External links
- {{Commonscatinline}}
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