Sandalore

CAS No. 65113-99-7

Sandalore( —— )

Catalog No. M28810 CAS No. 65113-99-7

Sandalore prolongs human hair growth by decreasing apoptosis and increasing the production of the anagen-prolonging growth factor IGF-1 in the outer root sheath. Sandalore is a selective agonist of olfactory receptor OR2AT4.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 42 In Stock
5MG 38 In Stock
10MG 57 In Stock
25MG 101 In Stock
50MG 147 In Stock
100MG 212 In Stock
200MG 318 In Stock
500MG 532 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Sandalore
  • Note
    Research use only, not for human use.
  • Brief Description
    Sandalore prolongs human hair growth by decreasing apoptosis and increasing the production of the anagen-prolonging growth factor IGF-1 in the outer root sheath. Sandalore is a selective agonist of olfactory receptor OR2AT4.
  • Description
    Sandalore prolongs human hair growth by decreasing apoptosis and increasing the production of the anagen-prolonging growth factor IGF-1 in the outer root sheath. Sandalore is a selective agonist of olfactory receptor OR2AT4.(In Vitro):Sandalore (500 μM) significantly reduced hair matrix keratinocyte apoptosis and retarded spontaneous hair follicle (HF) regression (catagen development) ex vivo.
  • In Vitro
    3-Campholenyl-2-butanol (500 μM; 6 days) retards spontaneous hair follicle (HF) regression (catagen development) ex vivo and significantly reduces hair matrix keratinocyte apoptosis.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    GABAA
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    65113-99-7
  • Formula Weight
    210.36
  • Molecular Formula
    C14H26O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (475.38 mM)
  • SMILES
    CC(CCC1C(C)(C)C(C)=CC1)C(C)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Taliani S, et al. Identification of anxiolytic/nonsedative agents among indol-3-ylglyoxylamides acting as functionally selective agonists at the gamma-aminobutyric acid-A (GABAA) alpha2 benzodiazepine receptor. J Med Chem. 2009 Jun 25;52(12):3723-34.
molnova catalog
related products
  • AEG 3482

    AEG 3482 is a potent antiapoptotic compound. AEG 3482 inhibits Jun kinase (JNK) activity through induced expression of heat shock protein 70 (HSP70). AEG 3482 directly binds HSP90, thereby facilitating HSF1-dependent expression of HSP70 and HSP25.

  • Tafasitamab

    Tafasitamab (XmAb5574) is an FC-modified humanized monoclonal antibody targeting the human B-cell surface antigen CD19 for the study of diffuse large B-cell lymphoma.

  • Tubulin inhibitor 32

    Tubulin inhibitor 32 is an orally active novel microtubule inhibitor with antiproliferative and antitumor activity, inhibits microtubule polymerization, induces apoptosis and cell cycle arrest in G2/M phase.