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626-69-7

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626-69-7 Usage

Uses

H-Ser(SO3H)-OH is used in methods and combinations for modulating tolerance to opiates, opioids or opioid analgesics and treating acute and chronic pain.

Definition

ChEBI: A non-proteinogenic L-alpha-amino acid that is the O-sulfo derivative of L-serine.

Check Digit Verification of cas no

The CAS Registry Mumber 626-69-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 626-69:
(5*6)+(4*2)+(3*6)+(2*6)+(1*9)=77
77 % 10 = 7
So 626-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO6S/c4-2(3(5)6)1-10-11(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1

626-69-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name L-serine O-sulfate

1.2 Other means of identification

Product number -
Other names serine sulfuric acid ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:626-69-7 SDS

626-69-7Upstream product

626-69-7Downstream Products

626-69-7Relevant articles and documents

Mechanism and Stereochemistry of the Activation of (2S)- and (2R)-Serine O-Sulfate as Suicide Inhibitors for Escherichia coli Glutamic Acid Decarboxylase

Rose, Janet E.,Leeson, Paul D.,Gani, David

, p. 3089 - 3094 (2007/10/02)

E. coli glutamic acid decarboxylase is inactivated by both enantiomers of the suicide inhibitor serine O-sulfate; inactivation by the (2S)-enantiomer involves Cα-H bond cleavage while inactivation by the (2R)-isomer involves Cα-decarboxylation.Both processes occur on the 4'-Re-face of the coenzyme, the opposite face to that utilised in physiological decarboxylation.

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