Euscaphic Acid
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Hodoodo CAT#: H112163

CAS#: 53155-25-2

Description: Euscaphic acid is a triterpene that inhibits the proliferation of CNE-1 and C666-1 nasopharyngeal carcinoma cells.


Chemical Structure

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Euscaphic Acid
CAS# 53155-25-2

Theoretical Analysis

Hodoodo Cat#: H112163
Name: Euscaphic Acid
CAS#: 53155-25-2
Chemical Formula: C30H48O5
Exact Mass: 488.35
Molecular Weight: 488.710
Elemental Analysis: C, 73.73; H, 9.90; O, 16.37

Price and Availability

Size Price Availability Quantity
1mg USD 355 2 Weeks
5mg USD 1100 2 Weeks
10mg USD 1950 2 Weeks
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Synonym: Euscaphic Acid

IUPAC/Chemical Name: (1R,2R,4aS,6aS,6bR,8aR,10S,11R,12aR,12bR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylic acid

InChi Key: OXVUXGFZHDKYLS-QUFHAEKXSA-N

InChi Code: InChI=1S/C30H48O5/c1-17-10-13-30(24(33)34)15-14-27(5)18(22(30)29(17,7)35)8-9-21-26(4)16-19(31)23(32)25(2,3)20(26)11-12-28(21,27)6/h8,17,19-23,31-32,35H,9-16H2,1-7H3,(H,33,34)/t17-,19-,20+,21-,22-,23-,26+,27-,28-,29-,30+/m1/s1

SMILES Code: C[C@@H]1CC[C@]2(C(O)=O)CC[C@@]3(C)[C@]4(C)CC[C@@]5([H])C(C)(C)[C@H](O)[C@H](O)C[C@]5(C)[C@@]4([H])CC=C3[C@]2([H])[C@]1(C)O

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: To be determined

Shelf Life: >2 years if stored properly

Drug Formulation: To be determined

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 488.71 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Shi C, Li Z, Wu Y, Li X, Li Y, Wei J, Li J, Zhang Y, Li L. Euscaphic acid and Tormentic acid protect vascular endothelial cells against hypoxia-induced apoptosis via PI3K/AKT or ERK 1/2 signaling pathway. Life Sci. 2020 Jul 1;252:117666. doi: 10.1016/j.lfs.2020.117666. Epub 2020 Apr 13. PMID: 32298737.


2: Dai W, Dong P, Liu J, Gao Y, Hu Y, Lin H, Song Y, Mei Q. Euscaphic acid inhibits proliferation and promotes apoptosis of nasopharyngeal carcinoma cells by silencing the PI3K/AKT/mTOR signaling pathway. Am J Transl Res. 2019 Apr 15;11(4):2090-2098. PMID: 31105820; PMCID: PMC6511751.


3: Li JJ, Li Y, Bai M, Tan JF, Wang Q, Yang J. Simultaneous determination of corosolic acid and euscaphic acid in the plasma of normal and diabetic rat after oral administration of extract of Potentilla discolor Bunge by high-performance liquid chromatography/electrospray ionization mass spectrometry. Biomed Chromatogr. 2014 May;28(5):717-24. doi: 10.1002/bmc.3098. Epub 2013 Dec 6. PMID: 24311372.


4: Jeong NH, Lee S, Choi YA, Song KS, Kim SH. Inhibitory Effects of Euscaphic Acid in the Atopic Dermatitis Model by Reducing Skin Inflammation and Intense Pruritus. Inflammation. 2022 Aug;45(4):1680-1691. doi: 10.1007/s10753-022-01652-x. Epub 2022 Mar 7. PMID: 35257273.


5: Kim IT, Ryu S, Shin JS, Choi JH, Park HJ, Lee KT. Euscaphic acid isolated from roots of Rosa rugosa inhibits LPS-induced inflammatory responses via TLR4-mediated NF-κB inactivation in RAW 264.7 macrophages. J Cell Biochem. 2012 Jun;113(6):1936-46. doi: 10.1002/jcb.24062. PMID: 22234926.


6: Chen J, Li WL, Wu JL, Ren BR, Zhang HQ. Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae. Pharmazie. 2008 Oct;63(10):765-7. PMID: 18972842.