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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
Molecular Weight:
387.47
MDL Number:
MFCD28975158
MOL File:
1649450-12-3.mol
Last updated:2023-05-18 11:31:03

ML352 Properties

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)

ML352 price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21878 ML-352 ≥98% 1649450-12-3 1mg $37 2024-03-01 Buy
Cayman Chemical 21878 ML-352 ≥98% 1649450-12-3 5mg $98 2024-03-01 Buy
Cayman Chemical 21878 ML-352 ≥98% 1649450-12-3 10mg $178 2024-03-01 Buy
TRC M425350 ML352 1649450-12-3 50mg $340 2021-12-16 Buy
ApexBio Technology B5897 ML352 1649450-12-3 10mg $201 2021-12-16 Buy
Product number Packaging Price Buy
21878 1mg $37 Buy
21878 5mg $98 Buy
21878 10mg $178 Buy
M425350 50mg $340 Buy
B5897 10mg $201 Buy

ML352 Chemical Properties,Uses,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

Preparation Products

ML352 Suppliers

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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]- 1649450-12-3