Cart
sales@molnova.com
Valnemulin HCl
CAS No. 133868-46-9
Valnemulin HCl( —— )
Catalog No. M17959 CAS No. 133868-46-9
Valnemulin HCl is a broad-spectrum bacteriostatic agent inhibiting protein synthesis in bacteria by binding to the peptidyl transferase component of the 50S subunit of ribosomes.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 40 | In Stock |
|
| 10MG | 31 | In Stock |
|
| 25MG | 48 | In Stock |
|
| 50MG | 57 | In Stock |
|
| 100MG | 91 | In Stock |
|
| 200MG | 133 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameValnemulin HCl
-
NoteResearch use only, not for human use.
-
Brief DescriptionValnemulin HCl is a broad-spectrum bacteriostatic agent inhibiting protein synthesis in bacteria by binding to the peptidyl transferase component of the 50S subunit of ribosomes.
-
DescriptionValnemulin HCl is a broad-spectrum bacteriostatic agent inhibiting protein synthesis in bacteria by binding to the peptidyl transferase component of the 50S subunit of ribosomes.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptorpeptidyl transferase
-
Research AreaInfection
-
Indication——
Chemical Information
-
CAS Number133868-46-9
-
Formula Weight601.28
-
Molecular FormulaC31H52N2O5S·HCl
-
Purity>98% (HPLC)
-
SolubilityDMSO : ≥ 26 mg/mL; 43.24 mM
-
SMILESCl.[H][C@@]12C(=O)CC[C@]11CC[C@@H](C)[C@@]2(C)[C@@H](C[C@@](C)(C=C)[C@@H](O)[C@@H]1C)OC(=O)CSC(C)(C)CNC(=O)[C@H](N)C(C)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Poulsen SM, et al. Mol Microbiol, 2001, 41(5), 1091-1099.
molnova catalog
related products
-
Mesna
Mesna(Uromitexan, Mesnex), a sulfhydryl compound that is used to reduce the incidence of hemorrhagic cystitis associated with certain chemotherapeutic agents.
-
4-Hydroxy-35-dimetho...
4-Hydroxy-35-dimethoxybenzyl alcohol is a kind of phenol with antiviral properties.
-
R 892
Potent and selective bradykinin B1 receptor antagonist (ID50 values are 2.8 and > 600 nM at B1 and B2 receptors respectively). Exhibits no intrinsic agonist activity and is resistant to aminopeptidase and kininase II (ACE) cleavage. Displays hypertensive activity in vivo.
