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  3. Eriocalyxin B

Eriocalyxin B is a diterpenoid compound that can be isolated from Chinese herb Isodon eriocalyx. Eriocalyxin B exhibits multiple activities, such as anti-cancer, anti-inflammatory, and inhibition of adipogenesis. Eriocalyxin B is capable of inducing apoptosis and autophagy in tumor cells. Eriocalyxin B can be used in the research of cancers, autoimmune diseases, and other conditions.

For research use only. We do not sell to patients.

Eriocalyxin B Chemical Structure

Eriocalyxin B Chemical Structure

CAS No. : 84745-95-9

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  • Biological Activity

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Description

Eriocalyxin B is a diterpenoid compound that can be isolated from Chinese herb Isodon eriocalyx. Eriocalyxin B exhibits multiple activities, such as anti-cancer, anti-inflammatory, and inhibition of adipogenesis. Eriocalyxin B is capable of inducing apoptosis and autophagy in tumor cells. Eriocalyxin B can be used in the research of cancers, autoimmune diseases, and other conditions[1][2][3][4][5].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
3.1 μM
Compound: 8
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
[PMID: 22624550]
HL-60 IC50
0.3 μM
Compound: 8
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
[PMID: 22624550]
MCF7 IC50
0.6 μM
Compound: 8
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
[PMID: 22624550]
SMMC-7721 IC50
0.8 μM
Compound: 8
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
[PMID: 22624550]
SW480 IC50
0.5 μM
Compound: 8
Cytotoxicity against human SW480 cells after 48 hrs by MTT assay
Cytotoxicity against human SW480 cells after 48 hrs by MTT assay
[PMID: 22624550]
In Vitro

Eriocalyxin B (0-3.5 μM; 7 days) inhibits adipogenesis (IC50: 2.745 μM) and suppresses the expression of key regulators of adipocyte differentiation, including C/EBPα, C/EBPβ, PPARγ, and FABP4 in 3T3-L1 preadipocytes[1].
Eriocalyxin B (1.25-3.5 μM; 16-48 h) induces G2/M phase arrest and inhibits the expression levels of cell cycle regulators in differentiated 3T3-L1 cells[1].
Eriocalyxin B (48 h) is cytotoxic to tumor cells such as A-549, MCF-7, SMMC-7721, SW-480, and HL-60, with IC50 values ranging from 0.3-3.1 μM[2].
Eriocalyxin B (0.35-2.25 μM; 24-72 h) inhibits cell viability, increases intracellular ROS production, and induces apoptosis and autophagy in MCF-7 and MDA-MB-231. The mechanism involves the inhibition of the Akt/mTOR/p70S6K signaling pathway[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: 3T3-L1 cells
Concentration: 1.25, 2.5, 3 and 3.5 μM
Incubation Time: 24 h
Result: Inhibited the levels of CDK1, CDK2, Cyclin A and Cyclin B1.
In Vivo

Eriocalyxin B (10 mg/kg; intraperitoneal injection; 27 days) exhibits anti-tumor activity in a mouse model of breast cancer[3].
Eriocalyxin B (10 mg/kg; intraperitoneal injection; 18-28 days) has an ameliorating effect in a mouse model of experimental autoimmune encephalomyelitis (EAE)[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female NOD/SCID mice aged 6-8 weeks old treated MDA-MB-231 cells[3]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection (i.p.); 27 days
Result: Led to a slower tumor growth rate and reduced final tumor weight.
Caused no significant change in body weight and liver enzyme levels in plasma (ALT, AST and LDH) after treatment.
Activated autophagy and apoptosis in vivo.
Animal Model: Female C57BL/6 mice aged 6-8 weeks old with EAE model[4]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection (i.p.); 11 days after or on the day of immunization for the treatment, continued until 28 days
Result: Led to amelioration of EAE, which correlated with reduced spinal cord inflammation and demyelination.
Abolished encephalitogenic T-cell responses to myelin oligodendrocyte glycoprotein in an adoptive transfer EAE model. The underlying mechanism of EriB-induced effects involved inhibition of T helper (Th) 1 and Th17 cell differentiation through Janus Kinase/Signal Transducer and Activator Of Transcription and Nuclear factor-κB signaling pathways as well as elevation of reactive oxygen species.
Molecular Weight

344.40

Formula

C20H24O5

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O[C@]1(OC2)[C@](C[C@]3([H])C4=C)(C4=O)[C@](CC3)([H])[C@]2(C(C=C5)=O)[C@](C5(C)C)([H])[C@@H]1O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Solvent & Solubility
In Vitro: 

DMSO : 20 mg/mL (58.07 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.9036 mL 14.5180 mL 29.0360 mL
5 mM 0.5807 mL 2.9036 mL 5.8072 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

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In Vivo Dissolution Calculator
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Purity & Documentation

Purity: 99.93%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.9036 mL 14.5180 mL 29.0360 mL 72.5900 mL
5 mM 0.5807 mL 2.9036 mL 5.8072 mL 14.5180 mL
10 mM 0.2904 mL 1.4518 mL 2.9036 mL 7.2590 mL
15 mM 0.1936 mL 0.9679 mL 1.9357 mL 4.8393 mL
20 mM 0.1452 mL 0.7259 mL 1.4518 mL 3.6295 mL
25 mM 0.1161 mL 0.5807 mL 1.1614 mL 2.9036 mL
30 mM 0.0968 mL 0.4839 mL 0.9679 mL 2.4197 mL
40 mM 0.0726 mL 0.3630 mL 0.7259 mL 1.8148 mL
50 mM 0.0581 mL 0.2904 mL 0.5807 mL 1.4518 mL
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Eriocalyxin B
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