SRD5A1-IN-1

CAS No. 2279077-93-7

SRD5A1-IN-1( —— )

Catalog No. M36063 CAS No. 2279077-93-7

SRD5A1-IN-1 is an inhibitor of steroid 5α-reductase type 1 (SRD5A1, IC50 = 1.44 μM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 150 In Stock
5MG 136 In Stock
10MG 198 In Stock
25MG 320 In Stock
50MG 434 In Stock
100MG 551 In Stock
200MG 728 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SRD5A1-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    SRD5A1-IN-1 is an inhibitor of steroid 5α-reductase type 1 (SRD5A1, IC50 = 1.44 μM).
  • Description
    SRD5A1-IN-1 (Compound 4) is a competitive and covalent steroid 5α-reductase type 1 (SRD5A1) inhibitor with an IC50 of 1.44 μM. SRD5A1-IN-1 modulates SRD5A1 function, leading to a lower level of dihydrotestosterone (DHT) production and SRD5A1 protein suppression.
  • In Vitro
    Western Blot Analysis Cell Line:HaCaT Concentration:0.5, 1, and 2.5 μM Incubation Time:12 h and 24 hResult:Showed a significant decrease in SRD5A1 protein expression at 1 and 2.5 μM at 24 h, whereas there were no significant changes in the level of SRD5A1 protein at 12 h.RT-PCR Cell Line:HaCaT Concentration:0.5, 1, and 2.5 μM Incubation Time:12 h and 24 h Result:Did not affect the mRNA expression of SRD5A1 at both incubation times.Cell Cytotoxicity Assay Cell Line:HaCaT Concentration:0.2, 0.5, 1, and 2.5 μM Incubation Time:24 h Result:Displayed no significant cytotoxicity (IC50: 29.99?±?8.69 μM).
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2279077-93-7
  • Formula Weight
    391.27
  • Molecular Formula
    C17H11F6NO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (255.58 mM; Ultrasonic )
  • SMILES
    N(C(/C=C/C1=CC(O)=C(O)C=C1)=O)C2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Lin A C K, et al. Caffeic acid N-[3, 5-bis (trifluoromethyl) phenyl] amide as a non-steroidal inhibitor for steroid 5α-reductase type 1 using a human keratinocyte cell-based assay and molecular dynamics. Scientific Reports, 2022, 12(1): 1-20.
molnova catalog
related products
  • N-phenylthiophene-2-...

    N-phenylthiophene-2-carboximidamide is a compound used as a molecular building block.

  • GSK9027

    GSK9027 (GR agonist 23a) is a nonsteroidal glucocorticoid receptor (GR) agonist.GSK9027 is a partial agonist on the 2×GRE reporter gene compared to dexamethasone and is less active than dexamethasone activity.

  • Memantine

    Memantine, an amantadine derivative with some dopaminergic effects, has been proposed as an antiparkinson agent and has may be used to treat moderate to severe Alzheimer's disease. It acts on the glutamatergic system by blocking NMDA receptors.