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Chemical Structure Cat. No. Product Name CAS No.
Temozolomide Chemical Structure
BCP03692 Temozolomide 85622-93-1
Temozolomide is a DNA-methylating agent. Temozolomide is an alkylating cytostatic drug.
D-Luciferin Chemical Structure
BCP15615 D-Luciferin 2591-17-5
D-Luciferin is a chemiluminescent substrate for luciferases. D-Luciferin produces fluorescence upon oxidation by luciferase in the presence of ATP.
Fasudil hydrochloride Chemical Structure
BCP26351 Fasudil hydrochloride 105628-07-7
Fasudil Hydrochloride is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Kis of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.
Fasudil Chemical Structure
BCP26821 Fasudil 103745-39-7
Fasudil, a Rho-kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats.
Vismodegib Chemical Structure
BCP01715 Vismodegib 879085-55-9
Vismodegib is a more potent novel and specific synthetic oral hedgehog pathway inhibitor with an IC50 of 3 nM.
BI 2536 Chemical Structure
BCP01743 BI 2536 755038-02-9
BI 2536 is Plk1 inhibitor with an IC50 of 0.83 nM.
Plerixafor Chemical Structure
BCP02337 Plerixafor 110078-46-1
Plerixafor (AMD3100) is a chemokine receptor antagonist for CXCR4 and CXCL12-mediated chemotaxis with IC50 of 44 nM and 5.7 nM, respectively.
Bedaquiline Chemical Structure
BCP02829 Bedaquiline 843663-66-1
Bedaquiline, also known as TMC207 and R207910, is a diarylquinoline anti-tuberculosis drug.
AZD4547 Chemical Structure
BCP02555 AZD4547 1035270-39-3
AZD4547 is an orally bioavailable inhibitor of the fibroblast growth factor receptor (FGFR) with potential antineoplastic activity.
GSK 650394 Chemical Structure
BCP08392 GSK 650394 890842-28-1
Serum- and glucocorticoid-regulated kinase 1 (SGK1) inhibitor (IC50 values are 62 and 103 nM for SGK1 and SGK2 respectively).
Conivaptan Chemical Structure
BCP07817 Conivaptan 210101-16-9
Conivaptan is a nonpeptide dual V1a/V2 AVP receptor antagonist.
Delamanid Chemical Structure
BCP07838 Delamanid 681492-22-8
Delamanid, a newer mycobacterial cell wall synthesis inhibitor, inhibits the synthesisi of mucolic acids, cruciala component of the cell wall of the Mycobacterium tuberculosis complex.
RGD (Arg-Gly-Asp) Peptides Chemical Structure
BCP12422 RGD (Arg-Gly-Asp) Peptides 99896-85-2
RGD Trifluoroacetate is a tripeptide that effectively triggers cell adhesion, addresses certain cell lines and elicits specific cell responses; binds to integrins. Sequence: Arg-Gly-Asp.
MK-2206 Chemical Structure
BCP20200 MK-2206 1032349-93-1
MK-2206 is a highly selective inhibitor of pan-Akt, namely, of all three Akt isoforms Akt1, Akt2, and Akt3.
Deferasirox Chemical Structure
BCP05341 Deferasirox 201530-41-8
Deferasirox is an iron chelator, also a cytochrome P450 3A4 inducer, Cytochrome P450 2C8 inhibitor, and Cytochrome P450 1A2 inhibitor.
AS1842856 Chemical Structure
BCP17382 AS1842856 836620-48-5
AS1842856 is a cell-permeable Foxo1inhibitor that blocks the transcription activity of Foxo1 with IC50 of 33 nM.
BMS-202 Chemical Structure
BCP16068 BMS-202 1675203-84-5
BMS-202 is an inhibitor of the PD-1/PD-L1 protein/protein interaction, mainly used for cancer treatment.
740Y-P Chemical Structure
BCP16353 740Y-P 1236188-16-1
740 Y-P is a cell-permeable phosphopeptide activator of PI3K.
Cabazitaxel Chemical Structure
BCP27641 Cabazitaxel 183133-96-2
A novel semi-synthetic taxane with antitumor activity used for the treatment of castration-resistant prostate cancer. A microtubule inhibitor.
Sorafenib Chemical Structure
BCP01767 Sorafenib 284461-73-0
Sorafenib is a multikinase inhibitor of Raf-1, B-Raf and VEGFR-2 with IC50 of 6 nM, 22 nM and 90 nM, respectively.
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