Ro 4468

Modify Date: 2025-08-25 22:08:18

Ro 4468 Structure
Ro 4468 structure
Common Name Ro 4468
CAS Number 49669-74-1 Molecular Weight 160.17100
Density 1.232g/cm3 Boiling Point 363.7ºC at 760 mmHg
Molecular Formula C6H12N2O3 Melting Point N/A
MSDS N/A Flash Point 173.7ºC

 Use of Ro 4468


Aviglycine (ABG-3168 free base) is an inhibitor of ethylene biosynthesis. Aviglycine (ABG-3168 (free base)) application delays natural flowering in pineapple[1].

 Names

Name aviglycine
Synonym More Synonyms

 Ro 4468 Biological Activity

Description Aviglycine (ABG-3168 free base) is an inhibitor of ethylene biosynthesis. Aviglycine (ABG-3168 (free base)) application delays natural flowering in pineapple[1].
Related Catalog
References

[1]. Ren-Huang Wang, et al. Delaying Natural Flowering in Pineapple Through Foliar Application of Aviglycine, an Inhibitor of Ethylene Biosynthesis.

 Chemical & Physical Properties

Density 1.232g/cm3
Boiling Point 363.7ºC at 760 mmHg
Molecular Formula C6H12N2O3
Molecular Weight 160.17100
Flash Point 173.7ºC
Exact Mass 160.08500
PSA 98.57000
LogP 0.28790
Index of Refraction 1.531
InChIKey USGUVNUTPWXWBA-JRIXXDKMSA-N
SMILES NCCOC=CC(N)C(=O)O

 Ro 4468Bioassay

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Name: Human Cystathionine gamma-lyase (Hydrogen sulphide synthesis)
Source: IUPHAR-DB
Target: Cystathionine gamma-lyase (Hydrogen sulphide synthesis) [Homo sapiens]
External Id: 1444_Human
Name: Inhibition of cystathionine gamma-lyase (unknown origin)
Source: ChEMBL
Target: Cystathionine gamma-lyase
External Id: CHEMBL4136611
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 Synonyms

Ro-4468
(2S,3E)-2-Amino-4-(2-aminoethoxy)-3-butenoic acid
TMP-941
Aviglycine
(2S,3E)-2-amino-4-(2-aminoethoxy)but-3-enoic acid
Ro 20-4468/001
ANTIBIOTIC RO 20-4468/001
AVG
(2S,3E)-2-amino-4-(2-aminoethoxy)-3-butenoic acid
(E)-L-2-[2-(2-aminoethoxy)vinyl]glycine
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid
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