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渥曼青霉素

From Penicillium funiculosum, ≥98% (HPLC and TLC), phosphatidylinositol 3-kinase inhibitor, powder

别名:

KY 12420

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关于此项目

经验公式（希尔记法）:
C23H24O8
化学文摘社编号:
19545-26-7
分子量:
428.43
NACRES:
NA.77
PubChem Substance ID:
24278777
UNSPSC Code:
12352207
MDL number:
MFCD00133927
Beilstein/REAXYS Number:
67676
Assay:
≥98% (HPLC and TLC)
Form:
powder
Quality level:
300
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产品名称

渥曼青霉素, from Penicillium funiculosum, ≥98% (HPLC and TLC)

biological source

Penicillium funiculosum

Quality Level

300

assay

≥98% (HPLC and TLC)

form

powder

color

off-white

solubility

DMSO: soluble, H2O: unstable

storage temp.

2-8°C

SMILES string

[H][C@@]12CCC(=O)[C@@]1(C)C[C@@H](OC(C)=O)C3=C2C(=O)c4occ5C(=O)O[C@H](COC)[C@@]3(C)c45

InChI

1S/C23H24O8/c1-10(24)30-13-7-22(2)12(5-6-14(22)25)16-18(13)23(3)15(9-28-4)31-21(27)11-8-29-20(17(11)23)19(16)26/h8,12-13,15H,5-7,9H2,1-4H3/t12-,13+,15+,22-,23-/m0/s1

InChI key

QDLHCMPXEPAAMD-QAIWCSMKSA-N

Gene Information

human ... PIK3CD(5293), PIK3CG(5294), PIK3R1(5295)

Biochem/physiol Actions

渥曼青霉素是一种有效和特异性磷脂酰肌醇 3-激酶（PI3-K）抑制剂，IC50 为 2-4 nM。抑制 PI3-K/Akt 信号转导级联可增强放射或血清剥夺引起的凋亡作用，并阻断细胞因子的抗凋亡作用。渥曼青霉素对 PI3-K 的抑制作用还阻断了胰岛素受体激活引起的许多短期代谢作用。
渥曼青霉素是一种有效和特异性磷脂酰肌醇 3-激酶（PI3-K）抑制剂，IC50 为 2-4 nM。

Features and Benefits

《受体分类和信号转导》手册的G蛋白质（异三聚体）和磷酸肌醇激酶页面有该化合物的介绍。想要浏览手册的其他页面， 请单击此处。
该化合物是环核苷酸和激酶磷酸酶生物学研究的特色产品。发现更多环核苷酸和激酶磷酸酶生物学特色产品。想要了解有关生物活性小分子在其他研究领域应用的更多信息，请访问 sigma.com/discover-bsm。

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pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Acute Tox. 2 Dermal

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
108M4006V
079M4044V
14171002
077M4083V
105M4020V

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S Nakanishi et al.
The Journal of biological chemistry, 267(4), 2157-2163 (1992-02-05)
We have found that a fungal strain, Talaromyces wortmannin KY12420, produces a potent inhibitor of smooth muscle myosin light chain kinase (MLCK). This active product, designated as MS-54, was isolated and purified from the culture broth of the fungus and
Alban R Pereira et al.
Journal of medicinal chemistry, 53(24), 8523-8533 (2010-12-03)
Analogues of the sponge meroterpenoid liphagal have been synthesized and evaluated for inhibition of PI3Kα and PI3Kγ as part of a program aimed at developing new isoform-selective PI3K inhibitors. One of the analogues, compound 24, with IC₅₀ values of 66
Alexander D Crawford et al.
PloS one, 6(2), e14694-e14694 (2011-03-08)
Natural products represent a significant reservoir of unexplored chemical diversity for early-stage drug discovery. The identification of lead compounds of natural origin would benefit from therapeutically relevant bioassays capable of facilitating the isolation of bioactive molecules from multi-constituent extracts. Towards
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全球贸易项目编号

货号GTIN
W1628-10MG04061833265956
W1628-1MG04061837488665
W1628-5MG04061837488672