Splitomicin

Modify Date: 2024-01-14 17:34:28

Splitomicin Structure
Splitomicin structure
Common Name Splitomicin
CAS Number 5690-03-9 Molecular Weight 198.217
Density 1.3±0.1 g/cm3 Boiling Point 383.6±17.0 °C at 760 mmHg
Molecular Formula C13H10O2 Melting Point 73-74.5℃
MSDS Chinese USA Flash Point 161.2±18.4 °C

 Use of Splitomicin


Splitomicin (Splitomycin) is a selective Sir2p inhibitor. Splitomicin inhibits NAD+-dependent HDAC activity of Sir2 protein. Splitomicin induces dose-dependent inhibition of HDAC in the yeast extract with an IC50 of 60 μM[1].

 Names

Name Splitomicin
Synonym More Synonyms

 Splitomicin Biological Activity

Description Splitomicin (Splitomycin) is a selective Sir2p inhibitor. Splitomicin inhibits NAD+-dependent HDAC activity of Sir2 protein. Splitomicin induces dose-dependent inhibition of HDAC in the yeast extract with an IC50 of 60 μM[1].
Related Catalog
Target

Sir2p:60 μM (IC50)

In Vivo Splitomicin (80 mg/kg with an intraperitoneal injection every 24 h for 5 days, in mice) enhances tissue factor (TF) activity in the arterial vessel wall and accelerates carotid artery thrombus formation in a photochemical injury model[2]. Animal Model: C57BL/6 mice aged 12-14 weeks weighing on average 27 g[2] Dosage: 80 mg/kg Administration: Intraperitoneal injection every 24 h for 5 days Result: Increased TF activity in mouse carotid artery as compared with the controls.
References

[1]. Bedalov A, et al. Identification of a small molecule inhibitor of Sir2p. Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15113-8.

[2]. Breitenstein A, et al. Sirt1 inhibition promotes in vivo arterial thrombosis and tissue factor expression in stimulated cells. Cardiovasc Res. 2011 Feb 1;89(2):464-72.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 383.6±17.0 °C at 760 mmHg
Melting Point 73-74.5℃
Molecular Formula C13H10O2
Molecular Weight 198.217
Flash Point 161.2±18.4 °C
Exact Mass 198.068085
PSA 26.30000
LogP 3.03
Appearance of Characters solid
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.656
Storage condition 2-8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2914399090

 Synthetic Route

~87%

Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: National University Corporation Nagoya University; ISHIHARA, Kazuaki; UYANIK, Muhammet; YASUI, Takeshi Patent: EP2684863 A1, 2014 ; Location in patent: Paragraph 0106 ;

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Journal of the American Chemical Society, , vol. 70, p. 2119

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Journal of the American Chemical Society, , vol. 70, p. 2119

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Journal of Chemical Research, Miniprint, , # 11 p. 1175 - 1184

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Journal of Organic Chemistry, , vol. 20, p. 1282,1285

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Angewandte Chemie - International Edition, , vol. 50, # 26 p. 5834 - 5838

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: US2005/79995 A1, ; Page/Page column 13 ;

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Splitomicin Structure

Splitomicin

CAS#:5690-03-9

Literature: Sb. Statei Obshch. Khim., , p. 610,613 Chem.Abstr., , p. 986 Journal of the American Chemical Society, , vol. 70, p. 2119

 Customs

HS Code 2914399090
Summary 2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles8

More Articles
SIRT1 decreases Lox-1-mediated foam cell formation in atherogenesis.

Eur. Heart J. 31 , 2301-9, (2010)

Endothelial activation, macrophage infiltration, and foam cell formation are pivotal steps in atherogenesis. Our aim in this study was to analyse the role of SIRT1, a class III deacetylase with import...

Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection.

PLoS ONE 4(6) , e6093, (2009)

The persistence of transcriptionally silent but replication-competent HIV-1 reservoirs in Highly Active Anti-Retroviral Therapy (HAART)-treated infected individuals, represents a major hurdle to virus...

Sirt1 inhibition promotes in vivo arterial thrombosis and tissue factor expression in stimulated cells.

Cardiovasc. Res. 89 , 464-72, (2011)

The mammalian silent information regulator-two 1 (Sirt1) blunts the noxious effects of cardiovascular risk factors such as type 2 diabetes mellitus and obesity. Nevertheless, the role of Sirt1 in regu...

 Synonyms

Splitomicin
1,2-dihydrobenzo[f]chromen-3-one
1,2-Dihydro-3H-benzo[f]chromen-3-one
MFCD03792600
3H-Naphtho[2,1-b]pyran-3-one, 1,2-dihydro-
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