Arylsulfatase

Names

[ Name ]:
Arylsulfatase

[Synonym ]:
EINECS 232-772-1
Arylsulfatase

Biological Activity

[Description]:

Arylsulfatase is a type I enzyme of prokaryotes and eukaryotes. Arylsulfatase is a sulfatase enzyme, is often used in biochemical studies[1].

[Related Catalog]:

Research Areas >> Others

[References]

[1]. Zhang J, et al. Sulfite may disrupt estrogen homeostasis in human via inhibition of steroid arylsulfatase. Environ Sci Pollut Res Int. 2022 Mar;29(13):19913-19917.

Chemical & Physical Properties

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H317-H334

[ Precautionary Statements ]:
P261-P280-P284-P304 + P340-P333 + P313-P342 + P311

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
42/43

[ Safety Phrases ]:
22-24/25-45-36/37/39-36/37-23

[ RIDADR ]:
UN3373 - class 6.2 Biological substance, Category B

[ WGK Germany ]:
3

Articles

Effects of the halophytes Tecticornia indica and Suaeda fruticosa on soil enzyme activities in a Mediterranean Sabkha.

Int. J. Phytoremediation 15(2) , 188-97, (2013)

In the present work, we studied the effectiveness of the predominant halophytes of Soliman sabkha (Tecticornia indica and Suaeda fruticosa) to promote soil biological activities and ecosystem producti...

Disposition of bisphenol AF, a bisphenol A analogue, in hepatocytes in vitro and in male and female Harlan Sprague-Dawley rats and B6C3F1/N mice following oral and intravenous administration.

Xenobiotica 45 , 811-9, (2015)

1. Bisphenol AF (BPAF) is used as a crosslinking agent for polymers and is being considered as a replacement for bisphenol A (BPA). 2. In this study, comparative clearance and metabolism of BPAF and B...

Proton-in-flight mechanism for the spontaneous hydrolysis of N-methyl O-phenyl sulfamate: implications for the design of steroid sulfatase inhibitors.

J. Org. Chem. 77(9) , 4450-3, (2012)

The hydrolysis of N-methyl O-phenyl sulfamate (1) has been studied as a model for steroid sulfatase inhibitors such as Coumate, 667 Coumate, and EMATE. At neutral pH, simulating physiological conditio...

Related Compounds

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