ML352
- Product Name
- ML352
- CAS No.
- 1649450-12-3
- Chemical Name
- ML352
- Synonyms
- ML352;CS-1661;VU-0476201;VU-0476201;CS-1661;ML-352;Benzamide, 4-methoxy-N-[[3-(1-methylethyl)-5-isoxazolyl]methyl]-3-[(1-methyl-4-piperidinyl)oxy]-
- CBNumber
- CB63040791
- Molecular Formula
- C21H29N3O4
- Formula Weight
- 387.47
- MOL File
- 1649450-12-3.mol
ML352 Property
- Boiling point:
- 538.1±50.0 °C(Predicted)
- Density
- 1.145±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- Soluble in DMSO
- form
- Powder
- pka
- 13.03±0.46(Predicted)
N-Bromosuccinimide Price
- Product number
- 21878
- Product name
- ML-352
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $37
- Updated
- 2024/03/01
- Product number
- 21878
- Product name
- ML-352
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $98
- Updated
- 2024/03/01
- Product number
- 21878
- Product name
- ML-352
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $178
- Updated
- 2024/03/01
- Product number
- M425350
- Product name
- ML352
- Packaging
- 50mg
- Price
- $340
- Updated
- 2021/12/16
- Product number
- B5897
- Product name
- ML352
- Packaging
- 10mg
- Price
- $201
- Updated
- 2021/12/16
ML352 Chemical Properties,Usage,Production
Uses
ML352 is a novel, noncompetitive inhibitor of the presynaptic choline transporter (1).
Biological Activity
the neurotransmitter acetylcholine (ach) plays a critical role in autonomic function, motor control, attention, learning, and memory, and reward. the high-affinity choline transporter (cht) is the ratelimiting determinant of ach synthesis, yet the transporter remains a largely undeveloped target for the detection and manipulation of synaptic cholinergic signaling. ml352 is a novel, noncompetitive inhibitor of the presynaptic choline transporter.
in vitro
at concentrations fully antagonized cht in transfected cells and nerve terminal preparations, ml352 exhibited no inhibition of acetylcholinesterase or cholineacetyltransferase and also lacked activity at dopamine, serotonin, and norepinephrine transporters, as well as many receptors and ion channels. ml352 exhibited noncompetitive choline uptake inhibition in intact cells and reduced the apparent density of hemicholinium-3 binding sites in membrane assays, indicating allosteric transporter interactions [1].
in vivo
dmpk studies revealed a high intravenous plasma clearance, a combination of the oral bioavailability and total brain concentrations indicate ml352 to be a suitable probe for studies of altered in vivo ach signaling and behavioral effects in rodents [2].
References
[1] ennis ea, wright j, retzlaff cl, mcmanus ob, lin z, huang x, wu m, li m, daniels js, lindsley cw, hopkins cr, blakely rd. identification and characterization of ml352: a novel, noncompetitive inhibitor of the presynaptic choline transporter. acs chem neurosci. 2015 mar 18;6(3):417-27.
[2] elizabeth ennis miss, jane wright, james tarr, charles locuson, corey hopkins, j daniels, craig lindsley and randy blakely. a novel approach to cholinergic signaling modulation: development and characterization of ml352, a novel, noncompetitive inhibitor of the presynaptic choline transporter. the faseb journal vol. 29 no. 1 supplement 932.6
ML352 Preparation Products And Raw materials
Raw materials
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