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Erinacine A Erinacin A

Product Name
Erinacine A Erinacin A
CAS No.
156101-08-5
Chemical Name
Erinacine A Erinacin A
Synonyms
(+)-Erinacin A;Erinacine A Erinacin A;Cyclohept[e]indene-8-carboxaldehyde, 2,3,3a,4,5,5a,6,7-octahydro-3a,5a-dimethyl-1-(1-methylethyl)-6-(β-D-xylopyranosyloxy)-, (3aR,5aR,6S)-
CBNumber
CB51470355
Molecular Formula
C25H36O6
Formula Weight
432.55
MOL File
156101-08-5.mol
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Erinacine A Erinacin A Property

Boiling point:
610.8±55.0 °C(Predicted)
Density 
1.24±0.1 g/cm3(Predicted)
solubility 
Acetonitrile: Soluble
Methanol: Soluble
form 
Solid
pka
13.01±0.70(Predicted)
color 
Light yellow to yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
E600090
Product name
(+)-ErinacinA
Packaging
5mg
Price
$23625
Updated
2021/12/16
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Erinacine A Erinacin A Chemical Properties,Usage,Production

Uses

(+)-Erinacin A is a diterpenoid derivative isolated from the mushroom Hericium erinaceum. It can increase the catecholamine and nerve growth factor (NGF) content in the central nervous system of rats.

in vivo

(+)-Erinacin A (1, 5 and 10 mg/kg, i.p.; single dose) inhibits neuronal cell death in SAM rats with transient stroke and suppresses the expression of inflammatory cytokines in SAM brain tissues with transient stroke[4]. (+)-Erinacin A (1, 2 and 5 mg/kg, i.p.; once a day for 5 days) significantly reduces tumor volume in DLD-1 xenograft mice[5].

Animal Model:DLD-1 xenograft mouse model[5].
Dosage:1, 2 and 5 mg/kg
Administration:Intraperitoneal injection (i.p.) once a day for 5 days
Result:Inhibited tumor volume by 60%, 32% and 26%.
Animal Model:SAM rats with transient stroke[4].
Dosage:1, 5 and 10 mg/kg
Administration:Intraperitoneal injection (i.p.) single dose
Result:Induced NeuN immune response in the entire brain region of SAM rats, and increased the number of NeuN cells. Inhibited the activation of iNOS and p38/MAPK pathways and the expression of CHOP and nitrotyrosine proteins in rat brain tissue.

References

[1] HIROKAZU KAWAGISHI ∗ . Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum[J]. Tetrahedron Letters, 1994, 35 10: Pages 1569-1572. DOI: 10.1016/s0040-4039(00)76760-8
[2] CHIEN-CHANG LU . Inhibitory effect of Erinacines A on the growth of DLD-1 colorectal cancer cells is induced by generation of reactive oxygen species and activation of p70S6K and p21[J]. Journal of Functional Foods, 2016, 21: Pages 474-484. DOI: 10.1016/j.jff.2015.12.031
[3] KAM-FAI LEE. Post-Treatment with Erinacine A, a Derived Diterpenoid of H. erinaceus, Attenuates Neurotoxicity in MPTP Model of Parkinson’s Disease.[J]. Antioxidants, 2020. DOI: 10.3390/antiox9020137
[4] PEI-CHIEN HSU . Erinacine A attenuates glutamate transporter 1 downregulation and protects against ischemic brain injury[J]. Life sciences, 2022, 306: Article 120833. DOI: 10.1016/j.lfs.2022.120833

Erinacine A Erinacin A Preparation Products And Raw materials

Raw materials

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Erinacine A Erinacin A Suppliers

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156101-08-5, Erinacine A Erinacin ARelated Search:


  • Erinacine A Erinacin A
  • Cyclohept[e]indene-8-carboxaldehyde, 2,3,3a,4,5,5a,6,7-octahydro-3a,5a-dimethyl-1-(1-methylethyl)-6-(β-D-xylopyranosyloxy)-, (3aR,5aR,6S)-
  • (+)-Erinacin A
  • 156101-08-5