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Cat. No.: HY-N10984

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Jacquilenin

Jacquilenin is a natural product that can be isolated from the flowers of Picris hieracioides L..

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

CAS No.: 7726-34-3
Formula: C₁₅H₁₈O₄
Molecular Weight:262.30

Storage:

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

Data Sheet (274 KB)

Jacquilenin Chemical Structure

CAS No.: 7726-34-3

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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

Jacquilenin is a natural product that can be isolated from the flowers of Picris hieracioides L.^[1].

Cellular Effect

Cell Line	Type	Value	Description	References
A549	IC₅₀	>100 μM Compound: 9	Cytotoxicity against human A549 cells after 24 hrs by MTT method Cytotoxicity against human A549 cells after 24 hrs by MTT method	[PMID: 17067155]
A549	IC₅₀	16.1 μM Compound: 9	Inhibition of ICAM1 induction in human A549 cells pretreated for 1 hr in presence of IL1alpha for 6 hrs Inhibition of ICAM1 induction in human A549 cells pretreated for 1 hr in presence of IL1alpha for 6 hrs	[PMID: 17067155]
A549	IC₅₀	20.1 μM Compound: 9	Inhibition of ICAM1 induction in human A549 cells pretreated for 1 hr in presence of TNFalpha for 6 hrs Inhibition of ICAM1 induction in human A549 cells pretreated for 1 hr in presence of TNFalpha for 6 hrs	[PMID: 17067155]
HepG2	IC₅₀	25 μM Compound: 9	Cytotoxicity against human Hep G2 cells Cytotoxicity against human Hep G2 cells	[PMID: 17067155]
WI-38	IC₅₀	2.7 μM Compound: 9	Cytotoxicity against human WI38 cells Cytotoxicity against human WI38 cells	[PMID: 17067155]
WI-38 VA13	IC₅₀	8.5 μM Compound: 9	Cytotoxicity against human VA13 cells Cytotoxicity against human VA13 cells	[PMID: 17067155]

Chemical Information

CAS No. 7726-34-3
Molecular Weight 262.30
Formula C₁₅H₁₈O₄
SMILES

O=C1[C@@H](C)[C@@](CCC(C)=C23)([H])[C@]([C@@]3([H])C(CO)=CC2=O)([H])O1
Structure Classification
- Terpenoids
- Sesquiterpenes
Initial Source
- Plants
- Compositae
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 (274 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]. Kanayama T, et al. Sesquiterpene lactones from flowers of Picris hieracioides L. Bulletin of the Chemical Society of Japan, 1988, 61(8): 2971-2972.

Calculators

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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.

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MOQ

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100 mg

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