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  • China
  • Product Name: Ginkgolide B
  • Price: ¥Inquiry/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng



15291-77-7

15291-77-7 structure
15291-77-7 structure
  • Name: Ginkgolide B
  • Chemical Name: Ginkgolide B
  • CAS Number: 15291-77-7
  • Molecular Formula: C20H24O10
  • Molecular Weight: 424.399
  • Catalog: Natural product Moss
  • Create Date: 2018-06-07 15:40:30
  • Modify Date: 2024-01-03 08:58:42
  • Ginkgolide B, an important active terpenoid from Ginkgo biloba leaves, is reported to increase cell viability and decrease cell apoptosis.IC50 value:Target:In vitro: Ginkgolide B (0.2 or 0.4 μg/ml) was added to the culture medium in vitro led to increases in cell viability and decreases in the number of hippocampal cells undergoing AAPH-induced apoptosis [1]. Ginkgolide B caused a dose-related protection against dysrhythmias; the antiarrhythmic effect of ginkgolide B was comparable to that of diltiazem and superior to the activity of metoprolol. Ginkgolide B can presumably prevent the re-entry mechanism involved in the development of ischemia-induced rhythm disturbances [2].In vivo: Oral administration of ginkgolide B (2 mg/kg/day, p.o.) caused a significant increase in cell viability and a highly significant decrease in the numbers of both spontaneously occurring and AAPH-induced apoptoses.

Name Ginkgolide B
Synonyms (1R,3R,6R,7S,8S,10R,11R,12R,13S,16S,17R)-6,12,17-Trihydroxy-16-methyl-8-(2-methyl-2-propanyl)-2,4,14,19-tetraoxahexacyclo[8.7.2.0.0.0.0]nonadecane-5,15,18-trione
ginkgolide b from ginkgo biloba leaves
6H-9,4a-(Epoxymethano)-3aH,9H-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-2,6,13(1H)-trione, 11-(1,1-dimethylethyl)hexahydro-1,4b,8-trihydroxy-5-methyl-, (1R,3aR,4aR,4bR,5S,8R,8aS,9R,11S,11aS)-
7-DEOXYGINKGOLIDE C
6H-9,4a-(Epoxymethano)-3aH,9H-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-2,6,13(1H)-trione, 11-(1,1-dimethylethyl)hexahydro-1,4b,8-trihydroxy-5-methyl-, (1R,3aR,4aR,4bR,5S,7aS,8R,8aR,9R,11S,11aS)-
6H-9,4a-(epoxymethano)-3aH,9H-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-2,6,13(1H)-trione, 11-(1,1-dimethylethyl)hexahydro-1,4b,8-trihydroxy-5-methyl-, (1R,3aR,4aR,4bR,5S,7aS,8aR,9R,11aS)-
(1R,3R,6R,7S,8S,10R,11R,12R,13S,16S,17R)-8-tert-Butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.0.0.0.0]nonadecane-5,15,18-trione
3-tert-butyl hexahydro-4,-7b-11 hydroxy-8-methyl
MFCD05662347
(1R,3R,7S,8S,10R,11R,12R,13S,16S,17R)-8-tert-Butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.0.0.0.0]nonadecane-5,15,18-trione
(1R,3R,6R,7S,8S,10R,11S,12R,16S,17R)-6,12,17-Trihydroxy-16-methyl-8-(2-methyl-2-propanyl)-2,4,14,19-tetraoxahexacyclo[8.7.2.0.0.0.0]nonadecane-5,15,18-trione
ginkgolide B from ginkgo leaves
GinkgolideB
Description Ginkgolide B, an important active terpenoid from Ginkgo biloba leaves, is reported to increase cell viability and decrease cell apoptosis.IC50 value:Target:In vitro: Ginkgolide B (0.2 or 0.4 μg/ml) was added to the culture medium in vitro led to increases in cell viability and decreases in the number of hippocampal cells undergoing AAPH-induced apoptosis [1]. Ginkgolide B caused a dose-related protection against dysrhythmias; the antiarrhythmic effect of ginkgolide B was comparable to that of diltiazem and superior to the activity of metoprolol. Ginkgolide B can presumably prevent the re-entry mechanism involved in the development of ischemia-induced rhythm disturbances [2].In vivo: Oral administration of ginkgolide B (2 mg/kg/day, p.o.) caused a significant increase in cell viability and a highly significant decrease in the numbers of both spontaneously occurring and AAPH-induced apoptoses.
Related Catalog
References

[1]. Jean R. Rapin, et al. In vitro and in vivo effects of an extract of Ginkgo biloba (EGb 761), ginkgolide B, and bilobalide on apoptosis in primary cultures of rat hippocampal neurons. Drug Development Research, 1998, 45 (1):1-43

[2]. Matyas Koltai, et al. Ginkgolide B protects isolated hearts against arrhythmias induced by ischemia but not reperfusion. European Journal of Pharmacology, 1989, 164 (2): 293-302

Density 1.6±0.1 g/cm3
Boiling Point 762.4±60.0 °C at 760 mmHg
Melting Point 280°C (dec.)
Molecular Formula C20H24O10
Molecular Weight 424.399
Flash Point 274.3±26.4 °C
Exact Mass 424.136932
PSA 148.82000
LogP 0.52
Vapour Pressure 0.0±5.8 mmHg at 25°C
Index of Refraction 1.651
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3

~95%

15291-77-7 structure

15291-77-7

Literature: Jaracz, Stanislav; Malik, Shahid; Nakanishi, Koji Phytochemistry, 2004 , vol. 65, # 21 SPEC. ISS. p. 2897 - 2902

~%

15291-77-7 structure

15291-77-7

Literature: Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958

~73%

15291-77-7 structure

15291-77-7

Literature: Weinges, Klaus; Schick, Hartmut Liebigs Annalen der Chemie, 1991 , # 1 p. 81 - 83

~%

15291-77-7 structure

15291-77-7

Literature: Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958

~%

15291-77-7 structure

15291-77-7

Literature: Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958

~%

15291-77-7 structure

15291-77-7

Literature: Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958

~%

15291-77-7 structure

15291-77-7

Literature: Liebigs Annalen der Chemie, , # 1 p. 81 - 83

~%

15291-77-7 structure

15291-77-7

Literature: Liebigs Annalen der Chemie, , # 1 p. 81 - 83

~%

15291-77-7 structure

15291-77-7

Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 14, # 22 p. 5673 - 5675
Precursor  2

DownStream  1