AC-262536|CAS 870888-46-3|DC Chemicals

Cas No.:	870888-46-3
Chemical Name:	1-Naphthalenecarbonitrile,4-[(3-endo)-3-hydroxy-8-azabicyclo[3.2.1]oct-8-yl]-
Synonyms:	AC262536;AC-262536;AC 262536;AC-262536
SMILES:	N#CC1=C2C=CC=CC2=C(N2[C@@H]3CC(O)C[C@H]2CC3)C=C1
Formula:	C₁₈H₁₈N₂O
M.Wt:	278.348324298859
Purity:	>98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Description:	AC-262536 is a selective and non-steroidal androgen receptor modulators (SARMs) with beneficial anabolic effects. AC-262536 exhibits potent agonist activity at the androgen receptor, with an affinity in the low nanomolar range (1-10 nM)[1].
In Vivo:	AC-262536 (3, 10, 30 mg/kg) reverses the luteinizing hormone (LH) spike in castrated rats[1]. Animal Model: Male Sprague-Dawley rats (200-225 g)[1] Dosage: 3, 10 and 30 mg/kg Administration: Administered subcutaneously; once daily for 14 consecutive days Result: Significantly decreased LH levels by about 40% at the 3 mg/kg dose. The ED50 was determined to be 2.8 mg/kg. At the 10 and 30 mg/kg doses, the effects of AC-262536 were significantly stronger than Testosterone Propionate (TP) : 1.91±0.32 ng/mL and 1.53±0.34 ng/mL vs. 3.12±0.69 ng/mL, respectively.
In Vitro:	AC-262536 dose-dependently inhibits dihydroxytestosterone (DHT)-induced proliferation of LNCaP. The effects are significant with 100 nM AC-262536 (%inhibition 47.2±12.2), and reaches a plateau with 1 μM treatment (%inhibition 50.7±7.6). Thus, AC-262536 can act as a functional antagonist in prostate cells[1].
References:	[1]. Fabrice Piu, et al. Pharmacological characterization of AC-262536, a novel selective androgen receptor modulator. J Steroid Biochem Mol Biol. 2008 Mar;109(1-2):129-37.

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