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SML0340

Sigma-Aldrich

Hydroxy-Dynasore

≥98% (HPLC)

Sinônimo(s):

3-Hydroxy-2-naphthalenecarboxylic acid 2-[(2,4,5-trihydroxyphenyl)methylene]hydrazide, 3-Hydroxy-N′-[(2,4,5-trihydroxyphenyl)methylidene]naphthalene-2-carbohydrazide

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5 MG
R$ 677,00
25 MG
R$ 2.712,00

R$ 677,00


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5 MG
R$ 677,00
25 MG
R$ 2.712,00

About This Item

Fórmula empírica (Notação de Hill):
C18H14N2O5
Número CAS:
Peso molecular:
338.31
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:
NACRES:
NA.77

R$ 677,00


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Nível de qualidade

Ensaio

≥98% (HPLC)

Formulário

powder

condição de armazenamento

protect from light

cor

faintly yellow to dark yellow

solubilidade

DMSO: >10 mg/mL

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Oc1cc(O)c(\C=N\NC(=O)c2cc3ccccc3cc2O)cc1O

InChI

1S/C18H14N2O5/c21-14-8-17(24)16(23)7-12(14)9-19-20-18(25)13-5-10-3-1-2-4-11(10)6-15(13)22/h1-9,21-24H,(H,20,25)/b19-9+

chave InChI

UAXHPUSKEWEOAP-DJKKODMXSA-N

Ações bioquímicas/fisiológicas

Hydroxy-Dynasore is a cell permeable and potent dynamin inhibitor that prevents uptake of recombinant botulinum neurotoxin A heavy chain binding domain (BoNT/A-Hc). Apparently, Hydroxy-Dynasore prevents dynamin-mediated fission of endocytic vesicles from the plasma membrane.
Hydroxy-Dynasore is a cell permeable and potent dynamin inhibitor.

Outras notas

Air sensitive.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Thao Nguyen et al.
Oncogene, 38(35), 6283-6300 (2019-07-18)
N-cadherin adhesion has been reported to enhance cancer and neuronal cell migration either by mediating actomyosin-based force transduction or initiating fibroblast growth factor receptor (FGFR)-dependent biochemical signalling. Here we show that FGFR1 reduces N-cadherin-mediated cell migration. Both proteins are co-stabilised
Keisuke Shirakura et al.
EMBO molecular medicine, 15(4), e16128-e16128 (2023-02-07)
Vascular endothelial protein tyrosine phosphatase (VE-PTP) influences endothelial barrier function by regulating the activation of tyrosine kinase receptor Tie2. We determined whether this action is linked to the development of atherosclerosis by examining the influence of arterial shear stress on
Alekhya Mazumdar et al.
International journal of molecular sciences, 21(15) (2020-08-06)
Tumor-secreted extracellular vesicles (EVs) have been identified as mediators of cancer-host intercellular communication and shown to support pre-metastatic niche formation by modulating stromal cells at future metastatic sites. While osteosarcoma, the most common primary malignant bone tumor in children and
Hui Yi Chew et al.
Cell, 180(5), 895-914 (2020-03-07)
A safe and controlled manipulation of endocytosis in vivo may have disruptive therapeutic potential. Here, we demonstrate that the anti-emetic/anti-psychotic prochlorperazine can be repurposed to reversibly inhibit the in vivo endocytosis of membrane proteins targeted by therapeutic monoclonal antibodies, as directly demonstrated
Yi-Zhi Wang et al.
Cell reports, 43(2), 113680-113680 (2024-01-19)
Extracellular vesicles (EVs) facilitate intercellular communication by transferring cargo between cells in a variety of tissues. However, how EVs achieve cell-type-specific intercellular communication is still largely unknown. We found that Notch1 and Notch2 proteins are expressed on the surface of

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