1. Anti-infection
  2. EBV
  3. 21-Hydroxyisoohchininolide

21-Hydroxyisoohchininolide is a salannin-type limonoid. 21-Hydroxyisoohchininolide inhibits lipopolysaccharide (LPS, HY-D1056)-induced nitric oxide production in mouse macrophages. 21-Hydroxyisoohchininolide exhibits cytotoxic activity against leukemia cells and breast cancer cells. 21-Hydroxyisoohchininolide suppresses phorbol 12-myristate 13-acetate (PMA) (HY-18739)-induced activation of Epstein-Barr virus early antigen in lymphocytes. 21-Hydroxyisoohchininolide can be used for the research of leukemia, breast cancer and inflammatory diseases.

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

21-Hydroxyisoohchininolide

21-Hydroxyisoohchininolide Chemical Structure

CAS No. : 1429747-14-7

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Description

21-Hydroxyisoohchininolide is a salannin-type limonoid. 21-Hydroxyisoohchininolide inhibits lipopolysaccharide (LPS, HY-D1056)-induced nitric oxide production in mouse macrophages. 21-Hydroxyisoohchininolide exhibits cytotoxic activity against leukemia cells and breast cancer cells. 21-Hydroxyisoohchininolide suppresses phorbol 12-myristate 13-acetate (PMA) (HY-18739)-induced activation of Epstein-Barr virus early antigen in lymphocytes. 21-Hydroxyisoohchininolide can be used for the research of leukemia, breast cancer and inflammatory diseases[1].

In Vitro

21-Hydroxyisoohchininolide (1×10-6-1×10-4 M; 48 h) exhibits cytotoxicity against HL60 human leukemia cells (IC50 = 22.7 ± 1.6 μM) and SK-BR-3 human breast cancer cells (IC50 = 91.5 ± 2.2 μM), but shows no cytotoxicity against A549 human lung cancer cells and AZ521 human stomach cancer cells after 48 h of treatment[1].
21-Hydroxyisoohchininolide (1×10-6-1×10-4 M; 2 h pre-incubation, 16 h LPS co-incubation) inhibits LPS-induced nitric oxide production in RAW 264.7 murine macrophage cells with an IC50 of 87.3 ± 4.5 μM, with no cytotoxicity to the cells after 16 h of LPS co-incubation[1].
21-Hydroxyisoohchininolide (10-1000 molar ratio relative to 32 pmol TPA) inhibits TPA-induced EBV-EA activation in Raji cells with an IC50 of 493 molar ratio relative to 32 pmol TPA, with 60% cell viability at the highest tested molar ratio of 1000:1[1].

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

Cell Cytotoxicity Assay[1]

Cell Line: HL60 human leukemia cells, AZ521 human stomach cancer cells, A549 human lung cancer cells, SK-BR-3 human breast cancer cells
Concentration: 1, 10 and 100 μM
Incubation Time: 48 h
Result: Exhibited cytotoxicity against HL60 cells with an IC50 of 22.7 μM.
Exhibited cytotoxicity against SK-BR-3 cells with an IC50 of 91.5 μM.
Showed no cytotoxicity (IC50 > 100 μM) against A549 and AZ521 cells.
Molecular Weight

634.71

Formula

C36H42O10

CAS No.
SMILES

C[C@]12[C@@]3([H])[C@](OC[C@@]3([C@@H](C[C@@H]2OC(/C=C/C4=CC=CC=C4)=O)O)C)([H])[C@]5([H])[C@]([C@@H]1CC(OC)=O)(C6=C(C)[C@H](C7=CC(OC7O)=O)C[C@@]6([H])O5)C

Structure Classification
Initial Source
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
21-Hydroxyisoohchininolide
Cat. No.:
HY-N18117
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