country

Change Language

EN - English
FR - Français
DE - Deutsch
ES - Español
JA - 日本語
KO - 한국어

Country or Region:

United States

Product Name	Size / Unit Price	Qty

Total: USD 0.00 Checkout

Cat. No.: HY-N1012

Copy Link Print Information

(-)-11,13-Dehydroeriolin

(-)-11,13-Dehydroeriolin (compound 9), a sesquiterpene lactone, is a nature product that could be isolated from Carpesium abrotanoides L. (-)-11,13-Dehydroeriolin has antiproliferative active. (-)-11,13-Dehydroeriolin can be used in research of cancer.

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

CAS No.: 87441-73-4
Formula: C₁₅H₂₀O₄
Molecular Weight:264.32

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (273 KB)

(-)-11,13-Dehydroeriolin Chemical Structure

CAS No.: 87441-73-4

Size

Price

Stock

Quantity

Amount: USD 0.00

* Please select Quantity before adding items.

Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- Cellular Effect
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

Cellular Effect

Cell Line	Type	Value	Description	References
A549	IC₅₀	2 μM Compound: 3	Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
DU-145	IC₅₀	0.38 μM Compound: 3	Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
HeLa	IC₅₀	1 μM Compound: 3	Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay	[PMID: 26316467]
HL-60	IC₅₀	0.18 μM Compound: 3	Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
K562	IC₅₀	1.7 μM Compound: 3	Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
MCF7	IC₅₀	4.1 μM Compound: 3	Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
MDCK	IC₅₀	10.8 μM Compound: 3	Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining	[PMID: 26316467]
MDCK	IC₅₀	11.6 μM Compound: 3	Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining	[PMID: 26316467]
MOLT-4	IC₅₀	1.2 μM Compound: 3	Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
NCI-H1975	IC₅₀	5.4 μM Compound: 3	Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
SGC-7901	IC₅₀	6.4 μM Compound: 3	Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay	[PMID: 26316467]
U-937	IC₅₀	0.21 μM Compound: 3	Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay	[PMID: 26316467]

Chemical Information

CAS No. 87441-73-4
Molecular Weight 264.32
Formula C₁₅H₂₀O₄
SMILES

C[C@@]1(C[C@@](OC2=O)([H])[C@](C2=C)([H])C[C@]3([H])[C@@]4(O3)C)[C@](CC4)([H])O1
Structure Classification
- Terpenoids
- Sesquiterpenes
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (273 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Yang BJ, et, al. Sesquiterpene lactones from Carpesium abrotanoides L. and their activity in inducing protective autophagy. Nat Prod Res. 2022 Jun;36(12):3207-3210. [Content Brief]

Calculators

Molarity Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Dilution Calculator

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

MOQ

Minimum order quantity

100 mg

Get Quote In-stock

Other size

Get Quote