(2S,3S)-2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butyric acid

98%

Reagent Code: #232977
fingerprint
CAS Number 120701-87-3

science Other reagents with same CAS 120701-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.26 g/mol
Formula C₇H₁₂N₄O₄S
badge Registry Numbers
MDL Number MFCD13191753
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in biochemical research as a specialized amino acid analog for studying enzyme mechanisms, particularly in sulfur-containing metabolic pathways. Its triazole and sulfino groups make it valuable in probing active site interactions in enzymes that process cysteine or methionine derivatives. Also explored as a potential component in the design of enzyme inhibitors due to its structural similarity to natural amino acids with added functional modifications. Shows utility in click chemistry applications when incorporated into peptide mimetics for labeling or bioconjugation studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿21,260.00
inventory 100mg
10-20 days ฿72,480.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2S,3S)-2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butyric acid
No image available

Used in biochemical research as a specialized amino acid analog for studying enzyme mechanisms, particularly in sulfur-containing metabolic pathways. Its triazole and sulfino groups make it valuable in probing active site interactions in enzymes that process cysteine or methionine derivatives. Also explored as a potential component in the design of enzyme inhibitors due to its structural similarity to natural amino acids with added functional modifications. Shows utility in click chemistry applications w

Used in biochemical research as a specialized amino acid analog for studying enzyme mechanisms, particularly in sulfur-containing metabolic pathways. Its triazole and sulfino groups make it valuable in probing active site interactions in enzymes that process cysteine or methionine derivatives. Also explored as a potential component in the design of enzyme inhibitors due to its structural similarity to natural amino acids with added functional modifications. Shows utility in click chemistry applications when incorporated into peptide mimetics for labeling or bioconjugation studies.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...