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United States

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Cat. No.: HY-119729

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Axinysterol

Axinysterol is a steroidal compound isolated from marine sponges of the genus Axinyssa, possessing anticancer activity. Axinysterol is employed in research within the field of oncology.

Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.

CAS No.: 151606-24-5
Formule: C₂₈H₄₂O₃
Masse moléculaire:426.63

Stockage:

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

Data Sheet (265 KB)

Axinysterol Chemical Structure

CAS No.: 151606-24-5

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Quantité

Amount: USD 0.00

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Use of MCE Products

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

Activité biologique
- Description
- Cellular Effect
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
Bioz

Activité biologique

Description

Axinysterol is a steroidal compound isolated from marine sponges of the genus Axinyssa, possessing anticancer activity. Axinysterol is employed in research within the field of oncology^[1]^[2].

Cellular Effect

Cell Line	Type	Value	Description	References
Huh-7	IC₅₀	26 μM Compound: 5	Cytotoxicity against human HuH7 cells assessed as cell viability after 72 hrs by WST-1 assay Cytotoxicity against human HuH7 cells assessed as cell viability after 72 hrs by WST-1 assay	[PMID: 26711144]

Chemical Information

CAS No. 151606-24-5
Masse moléculaire 426.63
Formule C₂₈H₄₂O₃
SMILES

C[C@@]12[C@]3([H])[C@]4(C=C[C@]1(C[C@H](CC2)O)OO4)[C@@]5([H])[C@](CC3)([C@@](CC5)([H])[C@H](C)/C=C/[C@H](C)C(C)=C)C
Structure Classification
- Steroids
Initial Source
- Marine natural products
- Sponge
formosan sponge
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

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

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (265 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)
Instruction de manipulation (2659 KB)

Références

[1]. Iguchi K, et al. A new 5α, 8α-epidioxy sterol from the Okinawan marine sponge of the Axinyssa genus[J]. Steroids, 1993, 58(9): 410-413. [Content Brief]

[2]. Su T R, et al. 5α, 8α-Epidioxysterols from a Formosan sponge, Axinyssa sp[J]. Natural Product Communications, 2013, 8(11): 1934578X1300801108. [Content Brief]

Calculators

Calculateur de molarité

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

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

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.

Bioz

Keywords

MOQ

Minimum order quantity

100 mg

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