(R)-Elagolix

目录号: A21184

GnRHR antagonist

(R)-Elagolix

(R)-Elagolix Chemical Structure

CAS NO. 834153-87-6

Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM).

库存: 现货

规格 价格 数量
2 mg
¥ 378.00
5 mg
¥ 756.00
10 mg
¥ 1,470.00
50 mg
¥ 4,326.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM).
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 15.83 mL 79.17 mL 158.33 mL
0.5 mM 3.17 mL 15.83 mL 31.67 mL
1 mM 1.58 mL 7.92 mL 15.83 mL
5 mM 0.32 mL 1.58 mL 3.17 mL

*The above data is based on the productmolecular weight 631.59. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A21184
作用机制 Antagonist (拮抗剂)
M. Wt 631.59
Formula C32H30F5N3O5
Purity >99%
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

CAS No. 834153-87-6
Synonyms NBI-56418, NBI56418, NBI 56418
SMILES FC1=C(C2=C(C)N(CC3=C(C(F)(F)F)C=CC=C3F)C(N(C[C@](C4=CC=CC=C4)([H])NCCCC(O)=O)C2=O)=O)C=CC=C1OC

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