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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 |
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| 5MG | 38 | In Stock |
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| 10MG | 57 | In Stock |
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| 25MG | 101 | In Stock |
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| 50MG | 147 | In Stock |
|
| 100MG | 212 | In Stock |
|
| 200MG | 318 | In Stock |
|
| 500MG | 532 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameSandalore
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NoteResearch use only, not for human use.
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Brief DescriptionSandalore 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.
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DescriptionSandalore 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.
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In Vitro3-Campholenyl-2-butanol (500 μM; 6 days) retards spontaneous hair follicle (HF) regression (catagen development) ex vivo and significantly reduces hair matrix keratinocyte apoptosis.
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In Vivo——
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorGABAA
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Research Area——
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Indication——
Chemical Information
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CAS Number65113-99-7
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Formula Weight210.36
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Molecular FormulaC14H26O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (475.38 mM)
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SMILESCC(CCC1C(C)(C)C(C)=CC1)C(C)O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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.
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