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Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
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- Epigenetics
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GPCR/G Protein
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Neuro Signaling Pathway
- Imidazoline Receptor
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Protease/Metabolic Enzyme
- COMT
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- Phospholipase
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
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Research Areas
- Metabolic Disease
- Neurological Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinazoline
- Pyrazole Series
- Boric acid
- Pyrimidine Series
- Quinoline Series
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
VDA
Chemical Structure | Cat. No. | Product Name | CAS No. |
---|
BCP09127 | Verubulin | 827031-83-4 | |
Verubulin, Radiation Therapy, and Temozolomide to Treat Patients With Newly Diagnosed Glioblastoma Multiforme.
|
BCP07754 | Ombrabulin | 181816-48-8 | |
Ombrabulin is a synthetic water-soluble analogue of combretastatin A4, derived from the South African willow bush (Combretum caffrum), with potential vascular-disrupting and antineoplastic activities.
|
BCP04084 | AZD-6126 | 219923-05-4 | |
AZD6126 was being investigated by AstraZeneca as a VDA (vascular disrupting agent).AZD-6126 is an angiogenesis inhibitor and tubulin inhibitor potentially for the treatment of solid tumours.
|
BCP04200 | BNC105P | 945771-96-0 | |
BNC105P is a benzofuran-based vascular disrupting agent (VDA) prodrug with potential anti-vascular and antineoplastic activities.
|
BCP19547 | BNC105 | 945771-74-4 | |
BNC105 is a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties.
|
BCP04238 | Verteporfin New | 129497-78-5 | |
Verteporfin, a benzoporphyrin derivative, is a medication used as a photosensitizer for photodynamic therapy.
|
BCP02849 | Plinabulin | 714272-27-2 | |
NPI-2358 (Plinabulin) is a novel vascular disrupting agent (VDA) with an IC50 of 15 nM against HT-29 cells.
|
BCP01949 | DMXAA | 117570-53-3 | |
DMXAA is a vascular disrupting agents (VDA) and competitive inhibitor of DT-diaphorase with Ki of 20 μM and IC50 of 62.5 μM in cell-free assays, respectively.
|