Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • Apoptosis
    (1)
  • Aurora Kinase
    (1)
  • COX
    (1)
  • FAK
    (1)
  • FLT
    (1)
  • IGF-1R
    (1)
  • MEK
    (1)
  • PDGFR
    (1)
  • PKC
    (1)
  • Others
    (8)
Filter
Search Result
Results for "

cs 1

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    17
    TargetMol | Activity
  • Peptide Products
    4
    TargetMol | inventory
  • Inhibitory Antibodies
    1
    TargetMol | natural
  • Dye Reagents
    1
    TargetMol | composition
  • Recombinant Protein
    12
    TargetMol | Activity
CS1
T603801448009-94-6
CS1 is a potent DNA Topo II α inhibitor that exhibits broad-spectrum antitumor effects in vitro, low toxicity in vivo, and potential anti-multidrug resistance capabilities. CS1 induces DNA damage, G2 M phase cell cycle arrest, and apoptosis [1].
  • $1,520
6-8 weeks
Size
QTY
Fibronectin CS1 Peptide acetate
TP1526L1
CS1 peptide is present within type III homology connecting segment (IIICS) as well as C-274 (cell-binding domain). Fibronectin CS1 Peptide lacks the Arg-Gly-Asp-containing domain, actively inhibits tumor metastases in spontaneous and experimental metastas
  • $80
In Stock
Size
QTY
TargetMol | Inhibitor Sale
Delcasertib acetate
T11740L
Delcasertib acetate is a selective δ protein kinase C (δPKC) inhibitor for the study of acute myocardial infarction and pain.
  • $297
In Stock
Size
QTY
Fibronectin CS1 Peptide
TP1526136466-51-8
he connecting segment 1 (CS-1) is a cell attachment domain located in the type III homology connecting segment (IIICS) of fibronectin. CS1 peptide of fibronectin, which lacks the Arg-Gly-Asp-containing domain, actively inhibits tumor metastases in spontan
  • Inquiry Price
Size
QTY
BMS-536924
T6419468740-43-4
BMS-536924 (BMS 536924) is an ATP-competitive IGF-1R IR inhibitor with IC50 of 100 nM 73 nM, modest activity for Mek, Fak, and Lck with very little activity for Akt1, MAPK1 2.
  • $33
In Stock
Size
QTY
Loxoprofen sodium
T0463L80382-23-6
Loxoprofen sodium (CS-600) is an effective and oral sodium inhibitor of COX-1 and COX-2 with IC50 of 6.5 and 13.5 μM, respectively. Loxoprofen sodium works by reducing the synthesis of prostaglandins from arachidonic acid. Loxoprofen sodium has anti-inflammatory and antitumor activity and can be used to treat atherosclerosis.
  • $39
In Stock
Size
QTY
CS-0047390
T92801025796-31-9
CS-0047390, also known as tert-Butyl-DCL, PSMA inhibitor, is a radiopaque peptide reagent.
  • $33
In Stock
Size
QTY
TargetMol | Inhibitor Sale
CS 2100
T22697913827-99-3
CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.
  • $35
In Stock
Size
QTY
TargetMol | Inhibitor Sale
CS-0777
T31107840523-39-9
CS-0777 is a potent, selective, and orally active S1P1 agonist (sphingosine 1-phosphate receptor modulator).
  • $3,320
10-14 weeks
Size
QTY
Octanoyl coenzyme A triammonium
T87054799812-82-1
Octanoyl coenzyme A triammonium, a medium-chain acyl coenzyme A, can inhibit citrate synthase (CS) and glutamate dehydrogenase (GDH) with IC50 values of 0.4-1.6 mM [1].
  • Inquiry Price
Inquiry
Size
QTY
EGFR-IN-70
T73154
EGFR-IN-70 is a potent EGFR inhibitor with IC 50 values of 23.6 and 307.5 nM for EGFR LR/TM/CS and EGFR WT , respectively. EGFR-IN-70 has anti-proliferative activity and suppresses phosphorylation of the EGFR . EGFR-IN-70 can be used for cancer research .
  • $1,520
Backorder
Size
QTY
Tigatuzumab
T76793918127-53-4
Tigatuzumab (CS-1008), a humanized IgG1 monoclonal antibody, specifically targets death receptor 5 (DR5), inducing apoptosis in cancer cells and inhibiting tumor growth in vivo. It holds potential for cancer research applications [1].
  • Inquiry Price
Size
QTY
1-39-Corticotropin (human)(TFA)
TP1242
Adrenocorticotropic Hormone (ACTH) (1-39) human (TFA), a member of the melanocortin family, is a melanocortin receptor agonist that stimulates corticosteroid production by the adrenals; melanocortin receptors are also located in the central nervous system (CNS) and on immune cells.
  • $198
Backorder
Size
QTY
Pactimibe sulfate
T62974608510-47-0
Pactimibe sulfate (CS-505) is a dual ACAT1 2 inhibitor, acting on ACAT1 (IC50: 4.9 μM) and ACAT2 (IC50: 3.0 μM). It inhibits oleoyl-CoA non-competitively (Ki: 5.6 μM) and significantly inhibits cholesterol ester formation (IC50: 6.7 μM). Pactimibe sulfate reduces plasma cholesterol activity and has anti-atherogenic potential.
  • $1,620
8-10 weeks
Size
QTY
Chst15-IN-1
T396312158198-77-5
Chst15-IN-1 is a powerful, reversible, covalent inhibitor of the Chst15 enzyme. It effectively suppresses the sulfation levels of chondroitin sulfate-E (CS-E) and other closely related sulfotransferases responsible for glycosaminoglycans (GAGs) synthesis. Acting as a selective sulfotransferase inhibitor, Chst15-IN-1 can attenuate the inhibitory actions of chondroitin sulfate proteoglycans (CSPGs), making it a promising candidate for enhancing neuronal repair.
  • $53
5 days
Size
QTY
Linafexor
T868122499656-04-9
Linafexor (CS-0159) acts as an agonist for the farnesoid X receptor (FXR) [1].
  • Inquiry Price
10-14 weeks
Size
QTY
Chiauranib
T355701256349-48-0
Chiauranib is a multi-target inhibitor against tumor angiogenesis and exhibits potent anticancer effects. Chiauranib potently inhibits the angiogenesis-related kinases (VEGFR1, VEGFR2, VEGFR3, PDGFRα and c-Kit), mitosis-related kinase Aurora B, and chronic inflammation-related kinase CSF1R, with IC50 values ranging from 1-9 nM.
  • $83
In Stock
Size
QTY