Pristimerin

For research use only. Not for therapeutic Use.

  • CAT Number: R016219
  • CAS Number: 1258-84-0
  • Molecular Formula: C30H40O4
  • Molecular Weight: 464.60
  • Purity: ≥95%
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Pristimerin(Cat No.:R016219)is a naturally occurring quinone methide triterpenoid extracted from Celastraceae plants, known for its potent anticancer, anti-inflammatory, and antioxidant properties. It has shown promising activity in cancer research, primarily by inducing apoptosis and inhibiting the proteasome and NF-κB pathways, making it a potential candidate for anticancer therapies. Additionally, pristimerin exhibits antimicrobial and antimalarial effects, expanding its relevance across therapeutic fields. Pristimerin is widely studied for its effects on cellular signaling pathways, supporting advancements in cancer treatment, inflammation control, and novel drug development from natural compounds.


CAS Number 1258-84-0
Synonyms

(9β,13α,14β,20α)-3-Hydroxy-9,13-dimethyl-2-oxo-24,25,26-trinoroleana-1(10),3,5,7-tetraen-29-oic Acid Methyl Ester; 3-Hydroxy-2-oxo-24-Nor-D:A-friedooleana-1(10),3,5,7-tetraen-29-oic Acid Methyl Ester; (20α)-3-Hydroxy-2-oxo-D:A-friedo-24-noroleana-1(

Molecular Formula C30H40O4
Purity ≥95%
Target Bacterial
Solubility Soluble in DMSO > 10 mM
Storage Store at -20°C
IUPAC Name methyl (2R,4aS,6aR,6aS,14aS,14bR)-10-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate
InChI InChI=1S/C30H40O4/c1-18-19-8-9-22-28(4,20(19)16-21(31)24(18)32)13-15-30(6)23-17-27(3,25(33)34-7)11-10-26(23,2)12-14-29(22,30)5/h8-9,16,23,32H,10-15,17H2,1-7H3/t23-,26-,27-,28+,29-,30+/m1/s1
InChIKey JFACETXYABVHFD-WXPPGMDDSA-N
SMILES CC1=C(C(=O)C=C2C1=CC=C3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4C[C@](CC5)(C)C(=O)OC)C)C)C)C)O
Reference

1: Yang H, Landis-Piwowar KR, Lu D, Yuan P, Li L, Reddy GP, Yuan X, Dou QP. Pristimerin induces apoptosis by targeting the proteasome in prostate cancer cells. J Cell Biochem. 2008 Jan 1;103(1):234-44. PubMed PMID: 17541980.<br />
2: Luo DQ, Wang H, Tian X, Shao HJ, Liu JK. Antifungal properties of pristimerin and celastrol isolated from Celastrus hypoleucus. Pest Manag Sci. 2005 Jan;61(1):85-90. PubMed PMID: 15593077.<br />
3: Monache FD, Bett&oacute;lo GV, de Lima OG, D/&#39;Albuquerque IL, de Barros Co&ecirc;lho JS. The structure of tingenone, a quinonoid triterpene related to pristimerin. J Chem Soc Perkin 1. 1973;22:2725-8. PubMed PMID: 4799459.

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