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Results for "

6-azauridine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7273
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6-Azuridine
6-Azuridine
TNU002254-25-1
6-Azauridine (6-Azuridine) is a purine nucleoside analog with a broad spectrum of antitumor activity, targeting malignant tumors of the inert lymphatic system and inducing apoptosis.6-Azuridine's anticancer mechanism is dependent on the inhibition of DNA synthesis.
  • $40
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6-Azauridine triphosphate
6-Azauridine 5′-triphosphate
T832706198-30-7
6-Azauridine triphosphate (6-Azauridine 5′-triphosphate), a nucleotide analog similar to uridine triphosphate, facilitates the study of RNA synthesis mechanisms and transcription regulation [1].
  • Inquiry Price
8-10 weeks
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QTY
2'-b-C-Methyl-6-azauridine
TNU0301172605-95-7
2'-b-C-Methyl-6-azauridine is a Nucleoside Derivative - 6-Aza-uridine; 2'-Modified nucleoside.
  • Inquiry Price
7-10 days
Size
QTY
2'-Deoxy-2'-fluoro-b-D-arabino-6-azauridine
TNU0302908129-24-8
2'-Deoxy-2'-fluoro-b-D-arabino-6-azauridine is a Nucleoside Derivative - 6-Aza-uridine; Fluoro-modified nucleoside; Arabino nucleoside.
  • Inquiry Price
7-10 days
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QTY
3'-Deoxy-3'-fluoro-6-azauridine
TNU0303439579-23-4
Nucleoside Derivatives - Fluoro-modified nucleosides, 3'-Modified nucleosides, 6-Aza-uridines
  • Inquiry Price
7-10 days
Size
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2',3',5'-Tri-O-benzoyl-2'-b-C-methyl-6-azauridine
TNU1078622379-83-3
2',3',5'-Tri-O-benzoyl-2'-b-C-methyl-6-azauridine is a nucleoside derivative, specifically a 2'-modified nucleoside of 6-aza-uridine.
  • Inquiry Price
7-10 days
Size
QTY
3',5'-Bis-O-benzoyl-2'-deoxy-2'-fluoro-b-D-arabino-6-azauridine
TNU10791013470-68-2
3',5'-Bis-O-benzoyl-2'-deoxy-2'-fluoro-β-D-arabino-6-azauridine is a nucleoside derivative featuring 6-aza-uridine, a fluoro modification, and arabino nucleoside properties.
  • Inquiry Price
7-10 days
Size
QTY
3'-Azido-3'-deoxy-6-azauridine
TNU1080
3'-Azido-3'-deoxy-6-azauridine (catalog number: TNU1080) is a valuable organic compound for life sciences research.
  • Inquiry Price
7-10 days
Size
QTY
2'-Deoxy-6-azauridine
TNU108120500-29-2
2'-Deoxy-6-azauridine is a useful organic compound for research related to life sciences. The catalog number is TNU1081 and the CAS number is 20500-29-2.
  • Inquiry Price
7-10 days
Size
QTY
2',3',5'-Tri-O-benzoyl-6-azauridine
TNU10921627-29-8
Nucleoside Derivatives - 6-Azauridines
  • Inquiry Price
7-10 days
Size
QTY
2-Thio-6-azauridine
T8984327089-56-1
  • Inquiry Price
7-10 days
Size
QTY
Sorafenib
Bay 43-9006
T0093L284461-73-0
Sorafenib (Bay 43-9006) is a multikinase inhibitor that targets Raf-1, B-Raf, VEGFR2, VEGFR3, VEGFR4, PDGFRβ, FLT3, c-Kit, and others (IC50=6/22/90/15/20/20/57/58 nM) with oral activity. It exhibits antitumor properties and can induce autophagy, apoptosis, and agonistic iron death.
  • $34
In Stock
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QTY
TargetMol | Citations Cited
Staurosporine
CGP 41251, Antibiotic AM-2282, AM-2282
T668062996-74-1
Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6/15/2/3/3000 nM) against PKC, PKA, c-Fgr, phosphorylase kinase and TAOK2. Staurosporine also induces apoptosis.
  • $56
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Rutin
Rutoside, Quercetin 3-O-rutinoside
T0795153-18-4
Rutin (Quercetin 3-O-rutinoside), a flavonoid, has a variety of biological activities including antiallergic, anti-inflammatory, antiproliferative, and anticarcinogenic properties.
  • $36
In Stock
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Acetylcysteine
N-Acetyl-L-cysteine, N-Acetylcysteine, N-Acetyl Cysteine, NAC, LNAC
T0875616-91-1
Acetylcysteine (NAC) is an N-acetyl derivative of cysteine, a ROS inhibitor and mucolytic agent. Acetylcysteine induces apoptosis, can be used to reduce mucus thickness, and has anti-influenza viral activity.
  • $33
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Corticosterone
Kendall's compound B, Corticosterone (From plants), 17-Deoxycortisol, 11β,21-Dihydroxyprogesterone
T0948L50-22-6
Corticosterone (Kendall's compound B) is an adrenocortical steroid with salocorticoid and glucocorticoid activity that is orally active. Corticosterone is involved in the regulation of energy, immune responses, and stress responses in the body.
  • $30
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TargetMol | Inhibitor Hot
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Tanzisertib
CC-930
T14895899805-25-5
Tanzisertib (CC-930) (CC-930) is a potent inhibitor of JNK1/2/3 with IC50s of 61/7/6 nM, respectively, with potential antifibrotic activity.
  • $35
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TargetMol | Inhibitor Hot
Deoxynivalenol
Vomitoxin, 4-Deoxynivalenol
T1509751481-10-8
Deoxynivalenol (Vomitoxin) is a mycotoxin produced by Fusarium spp. of the single trichothecene family and is commonly found in contaminated food and feed.Deoxynivalenol crosses the intestinal mucosa via a cellular bypass at the tight junctions.Deoxynivalenol transporters are unaffected by inhibitors of P-glycoprotein (PgP) or multidrug resistance-associated protein (MRP). Deoxynivalenol commonly causes diarrhea, vomiting, and gastrointestinal inflammation in humans and animals.
  • $89
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TargetMol | Inhibitor Hot
GB1107
(2R,3R,4S,5R,6R)-2-(3,4-dichlorophenyl)sulfanyl-6-(hydroxymethyl)-4-[4-(3,4,5-trifluorophenyl)triazol-1-yl]oxane-3,5-diol
T153721978336-61-6
GB1107 is an effective and selective Galectin-3 inhibitor with a Kd of 37 nM.
  • $54
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Resveratrol
trans-Resveratrol, SRT 501
T1558501-36-0
Resveratrol (SRT 501) is a polyphenolic natural product, a plant antitoxin with antioxidant and chemopreventive activities. Resveratrol has a wide range of targets including COX, SIRT, LOC, etc. Resveratrol induces autophagy and apoptosis.
  • $36
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Kainic acid
T15643487-79-6
Kainic acid is an excitatory amino acid receptor agonist (EC50=16.2 μM). Kainic acid is an effective excitatory toxic agent. Kainic acid induces epileptic seizures.
  • $35
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LMT-28
T157691239600-18-0
LMT-28 is an inhibitor of IL-6 and selectively inhibits IL-6-induced phosphorylation of gp130, STAT3, and JAK2.
  • $37
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Vorinostat
suberoylanilide hydroxamic acid, SAHA, MK0683
T1583149647-78-9
Vorinostat (SAHA) is a pan-histone deacetylase (HDAC) inhibitor (IC50=10 nM) with inhibitory activity against HDAC1/2/3/6/7/11. Vorinostat has antitumor activity, induces cell differentiation, blocks the cell cycle and induces apoptosis.
  • $44
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Empagliflozin
BI 10773
T1766864070-44-0
Empagliflozin (BI 10773) is an SGLT-2 inhibitor (IC50=3.1 nM) that is potent and selective, with more than 300-fold selectivity for SGLT-1/4/5/6. Empagliflozin is used for the treatment of type 2 diabetes.
  • $39
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TargetMol | Citations Cited