Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(1R,2S,3R,4S,5R)-4-acetamido-1-O-acetyl-2-O-phenoxythiocarbonyl-3-O-phenylcarbamoyl-1,2,3-cyclopentanetriol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

229306-11-0

Post Buying Request

229306-11-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

229306-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229306-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,3,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 229306-11:
(8*2)+(7*2)+(6*9)+(5*3)+(4*0)+(3*6)+(2*1)+(1*1)=120
120 % 10 = 0
So 229306-11-0 is a valid CAS Registry Number.

229306-11-0Relevant articles and documents

Synthesis and α-mannosidase inhibitory activity of three deoxy derivatives of mannostatin A

Ogawa, Seiichiro,Morikawa, Takayuki

, p. 1759 - 1765 (2007/10/03)

Three deoxy derivatives 2-4 of the α-mannosidase inhibitor mannostatin A (1) were synthesized, and their inhibition of Jack bean α-mannosidase was evaluated in order to elucidate the roles of each of the three hydroxyl groups of the inhibitor. The 1- and 2-deoxy derivatives 2 and 3 retained some inhibitory activity, although reduced by a factor of about 100 relative to the parent, whereas it was completely lost with the 3-deoxy derivative 4. Structure and activity relationships are discussed in the light of these findings.

Synthesis and biological evaluation of α-mannosidase inhibitory activity of three deoxy derivatives of mannostatin A

Ogawa, Seiichiro,Morikawa, Takayuki

, p. 1499 - 1504 (2007/10/03)

Three deoxy derivatives of α-mannosidase inhibitor mannostatin A have been synthesized and their inhibitory activity for Jack beans α-mannosidase evaluated in order to elucidate roles of each hydroxyl groups of the inhibitor. The 1- and 2-deoxy derivatives have preserved inhibitory potentials although they lowered the activity one-hundred fold compared to the parent, but the 3-deoxy derivative lost activity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 229306-11-0