Stavudine
CAS No. 3056-17-5
Stavudine( d4T | NSC 163661 )
Catalog No. M13973 CAS No. 3056-17-5
Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 42 | In Stock |
|
| 200MG | 59 | In Stock |
|
| 500MG | 87 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameStavudine
-
NoteResearch use only, not for human use.
-
Brief DescriptionStavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.
-
DescriptionStavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.(In Vitro):Stavudine (d4T) (50 μM) significantly reduces the expression of the NLRP3 inflammasome gene, IL-18 production and Aβ 42-stimulated cellular production of IL-1β in THP-1 derived macrophages.Stavudine (d4T) (50 μM) inhibits the assembly of the NLRP3 inflammasome complex and down-regulates the phagocytosis of Aβ 42 by macrophages.Stavudine (d4T) (10 μM, 7 or 14 days) significantly induced CEM cells apoptosis, especially after 14 days, and increases hydrogen peroxide levels.(In Vivo):Stavudine (d4T) (500 mg/kg, daily liquid, 2 weeks) can rapidly induce fat depletion and mild liver damage at high dose in male RjOrl Swiss mice.
-
In VitroStavudine (d4T) (50 μM) significantly reduces the expression of the NLRP3 inflammasome gene, IL-18 production and Aβ 42-stimulated cellular production of IL-1β in THP-1 derived macrophages.Stavudine (d4T) (50 μM) inhibits the assembly of the NLRP3 inflammasome complex and down-regulates the phagocytosis of Aβ 42 by macrophages.Stavudine (d4T) (10 μM, 7 or 14 days) significantly induced CEM cells apoptosis, especially after 14 days, and increases hydrogen peroxide levels.
-
In VivoStavudine (d4T) (500 mg/kg, daily liquid, 2 weeks) can rapidly induce fat depletion and mild liver damage at high dose in male RjOrl Swiss mice. Animal Model:Male RjOrl Swiss mice weighing 0.028-0.03 kg Dosage:500 mg/kg Administration:Daily liquid; 2 weeks Result:Reduced fat weight gain by 58%, 5.7 g in the control group and 4.9 g in the d4T treated group.Significantly elevated plasma ALT and LDH levels.Reduced plasma acetoacetic acid and beta-hydroxybutyric acid levels.Reduced liver and muscle mtDNA levels at high dose concentration of 500 mg/kg.
-
Synonymsd4T | NSC 163661
-
PathwayMicrobiology/Virology
-
TargetReverse Transcriptase
-
RecptorReverse Transcriptase
-
Research AreaInfection
-
Indication——
Chemical Information
-
CAS Number3056-17-5
-
Formula Weight224.21
-
Molecular FormulaC10H12N2O4
-
Purity>98% (HPLC)
-
SolubilityEthanol: 15 mg/mL (66.9 mM); DMSO: 45 mg/mL (200.7 mM)
-
SMILESOC[C@@H]1C=C[C@H](N2C(NC(C(C)=C2)=O)=O)O1
-
Chemical Name1-((2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Lea AP, Faulds D. Drugs. 1996 May;51(5):846-64.
molnova catalog
related products
-
Didanosine
Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.
-
GS-7340 Tenofovir al...
Tenofovir Alafenamide (GS-7340) is a prodrug of tenofovir, which is a reverse transcriptase inhibitor, used to treat HIV and Hepatitis B.
-
MK-6186
MK-6186 is a novel non-nucleoside reverse transcriptase inhibitor with antiviral activity for the study of viral infections.
Cart
sales@molnova.com