VPC-13566
CAS No. 218464-59-6
VPC-13566( VPC13566 | VPC 13566 )
Catalog No. M27935 CAS No. 218464-59-6
VPC-13566 is a BF3-specific small molecule, which effectively inhibited the androgen receptor transcriptional activity and displaced the BAG1L peptide from the BF3 pocket.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 191 | Get Quote |
|
| 10MG | 267 | Get Quote |
|
| 25MG | 466 | Get Quote |
|
| 50MG | 674 | Get Quote |
|
| 100MG | 954 | Get Quote |
|
| 500MG | 1881 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameVPC-13566
-
NoteResearch use only, not for human use.
-
Brief DescriptionVPC-13566 is a BF3-specific small molecule, which effectively inhibited the androgen receptor transcriptional activity and displaced the BAG1L peptide from the BF3 pocket.
-
DescriptionVPC-13566 is a BF3-specific small molecule, which effectively inhibited the androgen receptor transcriptional activity and displaced the BAG1L peptide from the BF3 pocket. VPC-13566 inhibits the growth of various prostate cancer cell lines and reduces the growth of AR-dependent prostate cancer xenograft tumors in mice.
-
In Vitro——
-
In Vivo——
-
SynonymsVPC13566 | VPC 13566
-
PathwayEndocrinology/Hormones
-
TargetAndrogen Receptor (AR)
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number218464-59-6
-
Formula Weight258.324
-
Molecular FormulaC18H14N2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (387.12 mM)
-
SMILESCc1cccc2c(c[nH]c12)-c1ccc2ccccc2n1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Anthony Boitano, et al. Aryl hydrocarbon receptor antagonists and methods of use thereof for treating various diseases. WO2020051207A2
molnova catalog
related products
-
AS-601811
AS-601811 is a steroidal 5α-reductase inhibitor and androgen receptor modulator used to study hair loss and acne.
-
Flutamide
Flutamide is an antiandrogen drug, with its active metablolite binding at androgen receptor.
-
DSRM-3716
Isoquinoline, 5-iodo- (9CI) is a potent and selective inhibitor of SARM1(IC50 = 75 nM) by preventing axonal degeneration and by allowing functional recovery of a metastable pool of damaged, but viable, axons.
Cart
sales@molnova.com