gedunin

CAS No.: 2753-30-2

product details:

Purity: 99%

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What is the gedunin ?

gedunin is , while it's Molecular Formula is C28 H34 O7 . Gedunin is a naturally occurring Hsp90 inhibitor. In vitro, Gedunin induces Hsp90-dependent client protein degradation and displays antiproliferative activity (IC50 values are 3.22, 8.84 and 16.8 μM in SKBr3, MCF-7 and CaCo-2 cancer cell lines respectively). Gedunin exhibits antimalarial activity against P. falciparum (IC50 values are 0.14 and 3.1 μM in parasite development and [3H]-hypoxanthine uptake assays respectively).

What is the CAS number for gedunin ?

The CAS number of gedunin is 2753-30-2.

More information of gedunin 2753-30-2 are:

Synonyms

16,17-Seco-24-nor-5a,13a,14b,17a-chola-1,20,22-trien-16-oic acid,14,15b:21,23-diepoxy-7a,17-dihydroxy-4,4,8-trimethyl-3-oxo-,16,17-lactone, acetate (8CI);D-Homo-24-nor-17-oxachola-1,20,22-triene-3,16-dione, 7-(acetyloxy)-14,15:21,23-diepoxy-4,4,8-trimethyl-,(5a,7a,13a,14b,15b,17aa)-; Gedunin (7CI); Gedunine; NSC 113497

CAS?Number

2753-30-2

Molecular Formula

C28 H34 O7

Molecular Weight

482.574

Density

1.28g/cm3

Melting Point

218 °C(Solv: methanol (67-56-1))

Boiling Point

594.3°Cat760mmHg

Flash Point

313.2°C

PSA

95.34000

LogP

4.56070

What is gedunin (2753-30-2) used for?

Gedunin is a natural inhibitor of the heat shock protein (Hsp90; Item Nos. 22734 | 22735) co-chaperone p23 that also inhibits Hsp90 expression in human teratocarcinomal NTERA-2 cells in vitro at 5 μg/ml. This tetranortriterpenoid, which is isolated from A. indica, binds to and blocks the chaperone activity of p23 to induce apoptosis in HeLa-PRB cells in vitro at a concentration of 20 μM. Gedunin inhibits breast cancer cell proliferation in vitro, with IC50 values of 8.84 and 3.22 μM in MCF-7 and SKBr-3 cells, respectively, and inhibits the growth of PANC-1 pancreatic cancer cells (IC50 = 25 μM) by targeting the sonic hedgehog pathway to induce apoptosis. It also exerts anti-inflammatory effects in vivo. In a mouse model of articular inflammation induced by zymosan , gedunin (0.05-0.5 mg/kg, i.p.) reduces edema formation and the production of inflammatory cytokines. Gedunin (0.5 mg/kg) also inhibits the pleural accumulation of eosinophils and activated T lymphocytes in an ovalbumin-sensitized mouse model of allergic inflammation when administered prior to ovalbumin rechallenge. It also targets the lipopolysaccharide binding site and thus blocks Toll-like receptor 4 (TLR4) signaling in macrophages in vitro at a concentration of 10 μM.

InChI:InChI=1/C28H34O7/c1-15(29)33-20-13-18-24(2,3)19(30)8-10-25(18,4)17-7-11-26(5)21(16-9-12-32-14-16)34-23(31)22-28(26,35-22)27(17,20)6/h8-10,12,14,17-18,20-22H,7,11,13H2,1-6H3/t17-,18+,20-,21?,22-,25-,26+,27+,28-/m1/s1

Articles related to gedunin:

Article

Source

Biocatalysis: Fungi mediated novel and selective 12β- or 17β-hydroxylation on the basic limonoid skeleton

Haldar, Saikat,Kolet, Swati P.,Thulasiram, Hirekodathakallu V.

supporting information, p. 1311 - 1317 (2013/06/27)

A New Limonoid Glycoside from the Stem Bark of Melia azedarach Linn.

Saxena, Meera,Srivastava, Santosh K.

, p. 1087 - 1088 (2007/10/02)

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