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jolkinolide A

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jolkinolide A Basic information

Product Name:
jolkinolide A
Synonyms:
  • jolkinolide A
  • (4aR,6aS,7aβ)-2,3,4,4aα,5,6,11aα,11b-Octahydro-4,4,8,11bβ-tetramethyl-1H-oxireno[1,10a]phenanthro[3,2-b]furan-9(7aH)-one
  • (5β,9β,10α)-8β,14β:12,16-Diepoxyabieta-11,13(15)-dien-16-one
  • 1H-Oxireno[1,10a]phenanthro[3,2-b]furan-9(7aH)-one, 2,3,4,4a,5,6,11a,11b-octahydro-4,4,8,11b-tetramethyl-, (4aR,6aS,7aR,11aS,11bR)-
CAS:
37905-07-0
MF:
C20H26O3
MW:
314.42
Mol File:
37905-07-0.mol
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jolkinolide A Chemical Properties

Boiling point:
479.5±45.0 °C(Predicted)
Density 
1.19±0.1 g/cm3(Predicted)
InChI
InChI=1S/C20H26O3/c1-11-15-12(22-17(11)21)10-14-19(4)8-5-7-18(2,3)13(19)6-9-20(14)16(15)23-20/h10,13-14,16H,5-9H2,1-4H3/t13-,14+,16-,19-,20+/m1/s1
InChIKey
OYXDHOVYZKWSRM-PHJMNMFVSA-N
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jolkinolide A Usage And Synthesis

Uses

Jolkinolide A can be used as a bone marrow mesenchymal stem cell osteogenic differentiation accelerator. It can be developed using matrix solid-phase dispersion coupled with high-performance liquid chromatography.

Definition

ChEBI: A natural product found in Euphorbia fischeriana.

in vivo

Jolkinolide A (40 mg/kg; i.p.; once every 3 days, for 2 months) inhibits the expression of the VEGF protein in A549 cell xenograft tumor model in mouse[1].

Animal Model:Female BALB/c nude mice (4-5 weeks old) injected with A549 cells[1]
Dosage:40 mg/kg
Administration:Intraperitoneal injection; once every 3 days for 2 months
Result:Significantly inhibited the expression of VEGF protein on the first, 10th, 30th, 45th, and 60th day of administration.

jolkinolide ASupplier

Nanjing Dasf Biotechnology Co., Ltd. Gold
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