Comparison

AL 082D06

Item no. CS-3964-25mg
Manufacturer ChemScene
Amount 25mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 256925-03-8
Similar products 256925-03-8
Available
Alternative Names
D06; D-06
CAS
256925-03-8
Purity
>98%
MWt
409.91
Formula
C23H24ClN3O2
Solubility
DMSO : 7.5 mg/mL (18.30 mM; Need ultrasonic and warming)
Clinical Information
No Development Reported
Pathway
GPCR/G Protein
Target
Glucocorticoid Receptor
Biological Activity
AL 082D06 is a selective, nonsteroidal glucocorticoid receptor (GR) antagonist with Ki of 210 nM. IC50 & Target: Ki: 210 nM (GR)[1] In Vitro: AL 082D06 (D06) binds specifically to GR with nanomolar affinity. Addition of AL 082D06 causes a dose-dependent decrease in transcriptional activation from the MMTV:Luc reporter stimulated with half-maximal DEX concentrations. AL 082D06 acts to antagonize reporter activity using several glucocorticoid-responsive promoter- reporter systems including the 3-kb tyrosine amino transferase (TAT) promoter and less complex promoters comprised of isolated glucocorticoid response element (GRE) sequences. AL 082D06 competes with 3H-Dex for baculovirus-expressed GR with nanomolar affinity. Other intracellular receptors (AR, ER, PR, and MR) have no affinity for AL 082D06 in a similarly structured binding assay with the appropriate receptor and tritiated ligand (>2500 nM). AL 082D06 has no activation efficacy on the progesterone, androgen, mineralocorticoid, retinoid, glucocorticoid, or estrogen receptors. AL 082D06 is very efficacious at antagonizing GR activity but exhibits much weaker efficacy when tested against the other steroid receptors in contrast to the reference antagonists used as controls[1].
Research Area
Endocrinology

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 25mg
Available: In stock
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