Cas no 15291-75-5 (Ginkgolide A)

Ginkgolide A is a diterpenoid lactone compound primarily derived from Ginkgo biloba leaves. As a key bioactive constituent, it exhibits notable pharmacological properties, particularly as a selective platelet-activating factor (PAF) receptor antagonist. This mechanism underpins its potential therapeutic applications in inflammation, cardiovascular disorders, and neuroprotection. Ginkgolide A is characterized by its unique cage-like molecular structure, contributing to its stability and specificity in biological interactions. Its high purity and well-defined chemical profile make it valuable for research in vascular biology, oxidative stress, and neurodegenerative diseases. The compound is typically isolated via chromatographic techniques, ensuring consistency for experimental and preclinical studies.
Ginkgolide A structure
Ginkgolide A structure
Product Name:Ginkgolide A
CAS No:15291-75-5
MF:C20H24O9
MW:408.399167060852
MDL:MFCD07437829
CID:50071
PubChem ID:354335522
Update Time:2026-01-04

Ginkgolide A Chemical and Physical Properties

Names and Identifiers

    • ginkgolide A
    • Ginkgolide A from Ginkgo biloba leaves
    • GINKGOLIDE A(AS)
    • GINKGOLIDE A(P) (AHP Verified) PrintBack
    • 1,7-DIDEOXYGINKGOLIDE C
    • BN 5202
    • gingkolide A
    • GINKGOBILOBAP.E.
    • Ginkgolid A
    • GINKGOLIDE A FROM GINKGO LEAVES
    • GINKGOLIDE A,GINKGO BILOBA L
    • ginkolide A
    • PRIMULIC ACID 1
    • [ "" ]
    • (1R,7S,11S,13R,17R)-8-Tert-butyl-6,17-dihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03
    • Ginkgolide A,(S)
    • (1R,3R,6R,7R,8S,10R,11S,13S,16S,17R)-8-tert-butyl-6,17-dihydroxy-16-methyl-2,4,14,19-tetraoxahexacyc
    • BN-52020
    • L000778
    • GinkgolideA
    • CHEBI:181554
    • 15291-75-5
    • FPUXKXIZEIDQKW-UHFFFAOYSA-N
    • NCGC00142512-01
    • NSC-603665
    • NCGC00017329-02
    • LS-14792
    • AKOS024463027
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-4,7b-dihydroxy-8-methyl-
    • 8-Tert-butyl-6,17-dihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
    • SCHEMBL14029426
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-4,7b-dihydroxy-8-methyl-, [1R-(1.alpha.,3.beta.,3aS*,4.beta.,6a.alpha.,7a.alpha.,7b.alpha.,8.alpha.,10a.alpha.,11aS*)]-
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3',2':3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione, 3-tert-butylhexahydro-4,7b-dihydroxy-8-methyl-
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta(c)furo(2,3-b)furo(3',2':3,4)cyclopenta(1,2-d)furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-4,7b-dihydroxy-8-methyl-, (1R,3S,3aS,4R,6aR,7aR,7bR,8S,10aS,11aS)-
    • CHEMBL1408113
    • (1S,3R,6R,7S,8S,10R,11S,13S,16S,17R)-8-Tert-butyl-6,17-dihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
    • NSC603665
    • C20H24O9
    • HMS2864P03
    • GINKGOLIDE A [MI]
    • AS-17563
    • BN 52020
    • 119460-49-0
    • Q27095718
    • BN52020
    • ginkgolide-A
    • SMR000544404
    • HMS2089P12
    • MLS001216228
    • GINKGOLIDE A (CONSTITUENT OF GINKGO)
    • SR-01000801389
    • MFCD00133365
    • DTXCID40820729
    • AB00827840-06
    • 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-dihydroxy-5-methyl-, (3aR,4aR,4bR,5S,7aS,8aS,9R,11S, 11aS)-
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta(c)furo(2,3-b)furo(3',2':3,4)cyclopenta(1,2-d)furan-5,9,12(4H)-trione, 3-tert-butylhexahydro-4,7b-dihydroxy-8-methyl-
    • NS00024980
    • BDBM50292287
    • Q-100178
    • DTXSID10873222
    • GINKGOLIDE A [WHO-DD]
    • CHEMBL465161
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta(c)furo(2,3-b)furo(3',2':3,4)cyclopenta(1,2-d)furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-4,7b-dihydroxy-8-methyl-, (1R,3S,3aS,4R,6aR,7aR,7bR,8S,10aS,11aS)-
    • 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta(c)furo(2,3-b)furo(3',2':3,4)cyclopenta(1,2-d)furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-4,7b-dihydroxy-8-methyl-, (1R-(1alpha,3beta,3aS*,4beta,6aalpha,7aalpha,7balpha,8alpha,10aalpha,11 aS*))-
    • AKOS030485969
    • SR-01000801389-2
    • GINKGOLIDE A (CONSTITUENT OF GINKGO) [DSC]
    • UNII-TAZ2DPR77B
    • DB06743
    • TAZ2DPR77B
    • Ginkgolide C; 1,7-Dideoxy
    • 8-TERT-BUTYL-6,17-DIHYDROXY-16-METHYL-2,4,14,19-TETRAOXAHEXACYCLO[8.7.2.0(1),(1)(1).0(3),?.0?,(1)(1).0(1)(3),(1)?]NONADECANE-5,15,18-TRIONE
    • DB-043164
    • Ginkgolide A
    • MDL: MFCD07437829
    • Inchi: 1S/C20H24O9/c1-7-12(22)26-10-6-17-9-5-8(16(2,3)4)18(17)11(21)13(23)28-15(18)29-20(17,14(24)27-9)19(7,10)25/h7-11,15,21,25H,5-6H2,1-4H3
    • InChI Key: FPUXKXIZEIDQKW-UHFFFAOYSA-N
    • SMILES: O1C2C3(C(C(=O)O2)O)C(C(C)(C)C)CC2C43CC3C(C(C)C(=O)O3)(C14C(=O)O2)O

Computed Properties

  • Exact Mass: 408.14200
  • Monoisotopic Mass: 408.14203234 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 29
  • Rotatable Bond Count: 1
  • Complexity: 893
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 7
  • Undefined Atom Stereocenter Count : 3
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 6
  • XLogP3: 0.6
  • Topological Polar Surface Area: 129
  • Molecular Weight: 408.4

Experimental Properties

  • Color/Form: Powder
  • Density: 1.5600
  • Melting Point: 300°C(dec.)(lit.)
  • Boiling Point: 710.1°C at 760 mmHg
  • Flash Point: 256.5±26.4 °C
  • Refractive Index: 1.631
  • Solubility: In vitro: DMSO solubility 100 mg/ml (244.86 mm; need ultrasonic)
  • PSA: 128.59000
  • LogP: -0.34030
  • Specific Rotation: -53°, (c = 0.5 in ethanol)
  • λmax: 219(EtOH)(lit.)
  • Solubility: Not determined

Ginkgolide A Security Information

Ginkgolide A Pricemore >>

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Ginkgolide A Production Method

Ginkgolide A Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:15291-75-5)Ginkgolide A
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Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:02
Price ($):discuss personally
Amadis Chemical Company Limited
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(CAS:15291-75-5)Ginkgolide A
Order Number:A883862
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Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 11:10
Price ($):355.0/182.0

Ginkgolide A Spectrogram

LC-MS QqQ
LC-MS
13C NMR
13C NMR
1H NMR 300 MHz DMSO
1H NMR

Additional information on Ginkgolide A

Introduction to Ginkgolide A (CAS No. 15291-75-5)

Ginkgolide A, a naturally occurring compound with the chemical formula C??H??O??, is widely recognized for its significant pharmacological properties. This compound is primarily derived from the Ginkgo biloba tree, a species renowned for its medicinal applications in traditional and modern medicine. The CAS number 15291-75-5 uniquely identifies Ginkgolide A in scientific and industrial contexts, facilitating its accurate classification and research utilization.

The structural complexity of Ginkgolide A, characterized by its lactone ring and multiple hydroxyl groups, contributes to its diverse biological activities. Over the years, extensive research has been conducted to elucidate its mechanisms of action and therapeutic potential. One of the most notable findings is its ability to inhibit platelet-activating factor (PAF), a key mediator in various inflammatory and immune responses. This inhibitory effect has garnered significant attention in the field of cardiovascular and neurodegenerative diseases.

Recent studies have highlighted the therapeutic implications of Ginkgolide A in neuroprotection. Research indicates that it may help mitigate oxidative stress and inflammation, which are pivotal factors in the pathogenesis of Alzheimer's disease and other neurodegenerative disorders. The compound's ability to cross the blood-brain barrier further enhances its potential as a therapeutic agent for central nervous system disorders. These findings have spurred interest in developing Ginkgolide A-based drugs for treating cognitive decline and memory loss.

In addition to its neuroprotective properties, Ginkgolide A has shown promise in cardiovascular health. Studies suggest that it can improve blood circulation by dilating blood vessels and reducing platelet aggregation. This makes it a candidate for managing conditions such as angina pectoris and peripheral artery disease. The compound's anti-inflammatory effects also contribute to its potential role in preventing atherosclerosis, a major risk factor for heart disease.

The pharmacokinetics of Ginkgolide A have been extensively studied to optimize its delivery and efficacy. Research has demonstrated that oral administration can yield significant bioavailability, although the compound's rapid metabolism necessitates careful dosing strategies. Advances in drug delivery systems, such as nanoparticle formulations, have shown promise in enhancing the stability and bioavailability of Ginkgolide A, thereby improving therapeutic outcomes.

The safety profile of Ginkgolide A has been thoroughly evaluated through preclinical and clinical trials. These studies have consistently shown that the compound is well-tolerated at therapeutic doses, with minimal side effects reported. However, as with any pharmacological agent, careful monitoring is essential to ensure patient safety. Future research aims to explore synergistic combinations with other drugs to enhance therapeutic efficacy while minimizing adverse effects.

The industrial production of Ginkgolide A has evolved significantly over the years, with advancements in extraction and synthesis techniques. Modern methodologies leverage biotechnological approaches to produce high-purity compounds efficiently. These innovations have not only improved the availability of Ginkgolide A but also reduced costs, making it more accessible for research and commercial applications.

The future prospects of Ginkgolide A are promising, with ongoing research exploring new therapeutic applications. Emerging evidence suggests potential benefits in treating metabolic disorders, such as diabetes and obesity, by modulating lipid metabolism and insulin sensitivity. Additionally, its anti-aging properties are being investigated in-depth, with preliminary results indicating that Ginkgolide A may help delay age-related physiological decline.

In conclusion, Ginkgolide A (CAS No. 15291-75-5) is a multifaceted compound with significant therapeutic potential across various medical domains. Its ability to modulate inflammatory pathways, protect against neurodegenerative diseases, enhance cardiovascular health, and exhibit anti-aging effects positions it as a valuable candidate for future pharmaceutical development. As research continues to uncover new applications and optimize delivery methods, Ginkgolide A is poised to play an increasingly important role in modern medicine.

Recommended suppliers
Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:15291-75-5)Ginkgolide A
LE10151
Purity:99%
Quantity:25KG,200KG,1000KG
Price ($):Inquiry
Email
Amadis Chemical Company Limited
(CAS:15291-75-5)Ginkgolide A
A883862
Purity:99%/99%
Quantity:500g/100mg
Price ($):355.0/182.0
Email