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Art. -Nr.: HY-N4055

Hennadiol

(Synonyms: Lup-20(29)-ene-3β,30-diol; Wallichenol)

Hennadiol (Lup-20(29)-ene-3β,30-diol) is a product that can be isolated from .

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Speicherung:

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

CAS. Nr.: 20065-99-0

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Use of MCE Products

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

Biologische Aktivität

Beschreibung

Hennadiol (Lup-20(29)-ene-3β,30-diol) is a product that can be isolated from ^[1].

Cellular Effect

Cell Line	Type	Value	Description	References
A2780	IC₅₀	>10 μM Compound: 22	Cytotoxicity against human A2780 cells after 96 hrs by MTT assay Cytotoxicity against human A2780 cells after 96 hrs by MTT assay	[PMID: 24467317]
A2780	IC₅₀	12.2 μg/mL Compound: 3	Cytotoxicity against human A2780 cells by clonogenic assay Cytotoxicity against human A2780 cells by clonogenic assay	[PMID: 16499334]
A549	IC₅₀	>10 μM Compound: 22	Cytotoxicity against human A549 cells after 96 hrs by MTT assay Cytotoxicity against human A549 cells after 96 hrs by MTT assay	[PMID: 24467317]
Bel-7402	IC₅₀	>10 μM Compound: 22	Cytotoxicity against human Bel7402 cells after 96 hrs by MTT assay Cytotoxicity against human Bel7402 cells after 96 hrs by MTT assay	[PMID: 24467317]
BGC-823	IC₅₀	>10 μM Compound: 22	Cytotoxicity against human BGC823 cells after 96 hrs by MTT assay Cytotoxicity against human BGC823 cells after 96 hrs by MTT assay	[PMID: 24467317]
BV-2	IC₅₀	>10 μM Compound: 22	Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method	[PMID: 24467317]
HCT-8	IC₅₀	>10 μM Compound: 22	Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay	[PMID: 24467317]

CAS. Nr. 20065-99-0
Molecular Weight 442.72
Formel C₃₀H₅₀O₂
SMILES

C[C@]12[C@@](CC[C@@]3([H])[C@]2(CC[C@]4([H])[C@@]3(CC[C@@H](C4(C)C)O)C)C)([H])[C@]5([H])[C@@](CC1)(CC[C@H]5C(CO)=C)C
Synonyms

Lup-20(29)-ene-3β,30-diol; Wallichenol
Structure Classification
- Terpenoids
- Triterpenes
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

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