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RN 1 dihydrochloride Sale

(Synonyms: LSD1 Inhibitor IV) 目录号 : GC10148

An irreversible LSD1 inhibitor

RN 1 dihydrochloride Chemical Structure

Cas No.:1781835-13-9

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50mg
¥6,647.00
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10mg
¥1,428.00
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产品描述

RN 1 dihydrochloride is a potent and selective inhibitor of LSD1 with IC50 value of 70 nM [1].

Lysine (K) -specific demethylase 1A (LSD1) is a flavin-dependent histone demethylase that demethylates mono- and di-methylated lysines and plays an important role in oocyte growth, embryogenesis and tissue-specific differentiation. LSD1 plays a role in acute myeloid leukemia (AML).

RN 1 dihydrochloride is a potent and selective LSD1 inhibitor. RN-1 inhibited monoamine oxidase MAO A and MAO B with IC50 values of 0.51 and 2.79 μM, respectively [1]. In baboon erythroid progenitor cells, RN-1 increased γ-globin expression [2].

In mice, RN-1 significantly impairs long-term memory but didn’t affect short-term memory [1]. In sickle cell disease (SCD) mice, RN-1 induced the expression of γ-globin and increased amounts of F cells and F reticulocytes [2]. In SCD mouse model, RN-1 induced HbF synthesis and increased amounts of mature erythrocytes and HbF-positive cells. Also, RN-1 reduced sickle cells and reticulocytes in the peripheral blood [3].

References:
[1].  Neelamegam R, Ricq EL, Malvaez M, et al. Brain-penetrant LSD1 inhibitors can block memory consolidation. ACS Chem Neurosci, 2012, 3(2): 120-128.
[2].  Rivers A, Vaitkus K, Ruiz MA, et al. RN-1, a potent and selective lysine-specific demethylase 1 inhibitor, increases γ-globin expression, F reticulocytes, and F cells in a sickle cell disease mouse model. Exp Hematol, 2015, 43(7): 546-553.e3.
[3].  Cui S, Lim KC, Shi L, et al. The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice. Blood, 2015, pii: blood-2015-02-626259.

Chemical Properties

Cas No. 1781835-13-9 SDF
别名 LSD1 Inhibitor IV
化学名 2-(((1R,2S)-2-(4-(benzyloxy)phenyl)cyclopropyl)amino)-1-(4-methylpiperazin-1-yl)ethanone dihydrochloride
Canonical SMILES CN1CCN(C(CN[C@]2([H])C[C@@]2([H])C3=CC=C(OCC4=CC=CC=C4)C=C3)=O)CC1.Cl.Cl
分子式 C23H29N3O2.2HCl 分子量 452.42
溶解度 <9.05mg/ml in Water; <9.05mg/ml in DMSO 储存条件 Store at -20°C
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1 mM 2.2103 mL 11.0517 mL 22.1034 mL
5 mM 0.4421 mL 2.2103 mL 4.4207 mL
10 mM 0.221 mL 1.1052 mL 2.2103 mL
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