42 Results for "

Vascular disrupting

" in MedChemExpress (MCE) Product Catalog:
Products (42)

42 Results for "Vascular disrupting" in MCE Product Catalog:

80
80 Publications Verification
Cat. No.: HY-10964
CAS No.: 117570-53-3
Purity:  99.93%
Synonyms: DMXAA; ASA-404
Research Areas:  

Infection Cancer

Vadimezan (DMXAA), the tumor vascular disrupting agent (tumor-VDA), is a murine agonist of the stimulator of interferon genes (STING) and also a potent inducer of type I IFNs and other cytokines. Vadimezan is unable to activate human STING. Vadimezan has anti-influenza virus H1N1-PR8 activities.
loading...
    loading...
17
17 Cited Publications
Cat. No.: HY-126010
CAS No.: 2253744-54-4
Purity:  99.93%
Target:  

Piezo Channel

Research Areas:  

Others

Dooku1 is a reversibly Yoda1 antagonist with IC50 value of 1.3 μM and 1.5 μM for 2 μM Yoda1-induced Ca 2+ entry HEK 293 cells and HUVECs, respectively. Dooku1 can disrupt Yoda1-induced Piezo1 channel activity and inhibit Yoda1-induced relaxation of aorta. Dooku1 can be used for vascular physiology and disease research .
loading...
    loading...
4
4 Cited Publications
Cat. No.: HY-14444
CAS No.: 714272-27-2
Purity:  ≥98.0%
Synonyms: NPI-2358
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Plinabulin (NPI-2358) is a vascular disrupting agen (VDA) against tubulin-depolymerizing with an IC50 of 9.8 nM against HT-29 cells . Plinabulin binds the colchicine binding site of β-tubulin preventing polymerization and has potent inhibitory to tumor cells .
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-Y0488A
CAS No.: 540-69-2
Synonyms: Ammonium formate
Formic acid ammonium is the ammonium salt form of formic acid, which is an endogenous metabolite. Formic acid ammonium activates the nitric oxide/cyclic guanosine monophosphate (NO/cGMP) signaling pathway in endothelial cells and inhibits calcium ion influx in vascular smooth muscle cells, resulting in vasomotor relaxation. Formic acid ammonium inhibits cytochrome C oxidase (CcO) and disrupts the electron transport chain, leading to ATP depletion. Formic acid ammonium can be used as a feed additive, which can lower the feed pH value, inhibit the growth of microorganisms (such as Escherichia coli, Salmonella), and extend the shelf life of the feed .
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-10498
CAS No.: 917111-44-5
Purity:  99.50%
Synonyms: CYT-997
Lexibulin (CYT-997) is a potent and orally active tubulin polymerisation inhibitor with IC50s of 10-100 nM in cancer cell lines; with potent cytotoxic and vascular disrupting activity in vitro and in vivo . Lexibulin induces cell apoptosis and induces mitochondrial ROS generation in GC cells .
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-125864B
CAS No.: 9001-32-5
Target:  

MMP Cadherin

Murine Fibrinogen is a native fibrinogen derived from mouse plasma. Murine Fibrinogen acts as a cerebrovascular permeability enhancer. Murine Fibrinogen activates matrix metalloproteinase-9 (MMP-9), downregulates the expression of vascular endothelial cadherin (VE-cadherin), and upregulates the expression of plasmalemmal vesicle-associated protein-1 (PV-1). Murine Fibrinogen increases macromolecular leakage from pial veins, thereby disrupting the microvascular integrity of cerebral blood vessels. Murine Fibrinogen can be used in studies related to cerebrovascular dysfunction .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-116940
CAS No.: 365542-77-4
Purity:  99.37%
Target:  

Oct3/4 Notch STAT

Research Areas:  

Cancer

Sm4 is a selective and orally active SOX18 inhibitor. Sm4 inhibits SOX18-DNA binding (IC50 = 97.5 μM); Sm4 disrupts the SOX18-RBPJ protein-protein interaction (IC50 = 42.3 μM). Sm4 blocks SOX18 DNA binding, disrupts multiple SOX18 protein-protein interactions with RBPJ, DDX1, DDX17, ILF3, SOX7 and STAT1, modulates SOX18 chromatin binding dynamics. Sm4 exerts anti‑angiogenic and anti‑lymphangiogenic effects, reduces tumor vascular density, triggers vascular defects in zebrafish, prolongs survival in mouse metastatic cancer models. Sm4 can be used for the research of breast cancer .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-N2173
CAS No.: 93675-88-8
Forsythoside E is a phenylethanoid glycoside compound. Forsythoside E can be isolated from Shuanghuanglian. Forsythoside E does not induce vascular leakage or promote histamine release in mice. Forsythoside E does not cause pseudo-allergic reactions .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-16114
CAS No.: 945771-74-4
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

BNC105 is a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties.
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-B2062
CAS No.: 1861-32-1
Synonyms: Dimethyl tetrachloroterephthalate
Chlorthal-dimethyl (Dimethyl tetrachloroterephthalate) is a plant growth regulator. Chlorthal-dimethyl affects cell division and differentiation, interfering with the normal development of vascular tissue. Chlorthal-dimethyl causes localized swelling of tomato hypocotyls and disrupts normal mitosis in germinating millet seedlings .
loading...
    loading...
Cat. No.: HY-113205
CAS No.: 26441-05-4
Purity:  ≥99.0%
Synonyms: 15-keto-PGE2
15-keto-Prostaglandin E2 (15-keto-PGE2) is an endogenous PGE2 metabolite. 15-keto-Prostaglandin E2 inhibits STAT3 activation by binding to the Cys259 residue of STAT3. 15-keto-Prostaglandin E2 binds to and stabilizes EP2 and EP4 receptors. 15-keto-Prostaglandin E2 inhibits the growth and progression of breast cancer cells. 15-keto-Prostaglandin E2 activates PPAR-γ and promotes fungal growth. 15-keto-Prostaglandin E2 disrupts glomerular vascularization during zebrafish development and reduces the surface area of the glomerular filtration barrier .
loading...
    loading...
Cat. No.: HY-N3677
CAS No.: 14351-29-2
Dammarenediol II is a ginsenoside precursor . Dammarenediol II reduces the activity of O-GlcNAc transferase (OGT) and downregulates the global O-GlcNAcylation level. Dammarenediol II inhibits the phosphorylation of Akt, mTOR and GSK3β. Dammarenediol II inhibits human carboxylesterase activity, VEGF-induced ROS production, stress fiber formation and vascular endothelial cadherin disruption. Dammarenediol II promotes cell apoptosis (apoptosis), increases the levels of cleaved PARP1 and p53, and inhibits retinal microvascular leakage. Dammarenediol II can be used in studies related to liver cancer and diabetic retinopathy .
loading...
    loading...
Cat. No.: HY-B0263S
CAS No.: 1190007-20-5
Synonyms: 2-(4-Thiazolyl)benzimidazole-d4
Thiabendazole-d4 is a deuterated form of Thiabendazole, which is an antiseptic, antifungal and antiparasitic agent .
loading...
    loading...
Cat. No.: HY-N2558
CAS No.: 19668-69-0
Murrayone is a coumarin compound with antifungal and antiplatelet activities. Murrayone disrupts fungal redox homeostasis, impairs cell membrane integrity, inhibits sporulation, spore germination and hyphal growth, and causes morphological damage to fungal cells. Murrayone reduces the disease severity of blueberry fruits infected with Botrytis cinerea. Murrayone can be used in studies related to fungal infections and vascular diseases .
loading...
    loading...
Cat. No.: HY-121287
CAS No.: 1689-83-4
Purity:  ≥98.0%
Target:  

Herbicide

Research Areas:  

Cardiovascular Disease

Ioxynil is an herbicide that act as endocrine disruptor. Ioxynil can disrupt vascular and heart development in zebrafish .
loading...
    loading...
Cat. No.: HY-13598
CAS No.: 1188371-47-2
Purity:  98.47%
Synonyms: CKD-516
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Valecobulin (CKD516) is a valine proagent of (S516) and a vascular disrupting agent (VDA). Valecobulin is a potent β-tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors .
loading...
    loading...
Cat. No.: HY-16147
CAS No.: 288847-35-8
Synonyms: Oxi4503; CA1P; Combretastatin A1 diphosphate
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Combretastatin A1 phosphate (Oxi4503) is a potent vascular disruptive agent. Combretastatin A1 phosphate exerts anti-angiogenic effects on tumors. Combretastatin A1 phosphate has the potential for the research of pancreatic neuroendocrine tumors .
loading...
    loading...
Cat. No.: HY-13598A
CAS No.: 1240321-53-2
Purity:  98.46%
Synonyms: CKD-516 hydrochloride
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Valecobulin hydrochloride (CKD-516 hydrochloride) is a valine proagent of S516 (HY-130233) and a vascular disrupting agent (VDA). Valecobulin hydrochloride is a potent β-tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors .
loading...
    loading...
Cat. No.: HY-15855
CAS No.: 404886-32-4
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Fosbretabulin (tromethamine), also known as combretastatin A4 phosphate (CA4P), is a vascular disrupting agent evaluated for its efficacy against anaplastic thyroid carcinoma (ATC). It targets tumor neovasculature, causing acute and reversible reductions in tumor blood flow and central necrosis .
loading...
    loading...
Cat. No.: HY-10964R
CAS No.: 117570-53-3
Synonyms: DMXAA (Standard); ASA-404 (Standard)
Vadimezan (Standard) (DMXAA (Standard)) is the analytical standard of Vadimezan (HY-10964). This product is intended for research and analytical applications. Vadimezan (DMXAA; ASA-404), the tumor vascular disrupting agent (tumor-VDA), is a murine agonist of the stimulator of interferon genes (STING) and also a potent inducer of type I IFNs and other cytokines. Vadimezan is unable to activate human STING. Vadimezan has anti-influenza virus H1N1-PR8 activities.
loading...
    loading...