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TTA-Q6

CAT: 0804-HY-10388-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-10388-01Size:5 mg
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Description
TTA-Q6 is a selective T-type Ca2+ channel antagonist, which can be used in the research of neurological disease[1].
CAS Number
910484-28-5
UNSPSC
12352005
Target
Calcium Channel
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/TTA-Q6.html
Concentration
10mM
Purity
99.97
Solubility
DMSO : 125 mg/mL (ultrasonic)
Smiles
N#CC1=CC=C([C@]2(C3CC3)N(CC(F)(F)F)C(NC4=C2C=C(Cl)C=C4)=O)C=C1
Molecular Formula
C20H15ClF3N3O
Molecular Weight
405.80
References & Citations
[1]Schlegel KA, et al. Discovery and expanded SAR of 4,4-disubstituted quinazolin-2-ones as potent T-type calcium channel antagonists. Bioorg Med Chem Lett. 2010 Sep 1;20 (17) :5147-52.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
T-type calcium channel

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Alternative Products

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MBS5754065TTA-Q6
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A21360-50TTA-Q6 50mg
A21360-25TTA-Q6 25mg
A21360-1TTA-Q6 1mg
A21360-10TTA-Q6 10mg
A21360-100TTA-Q6 100mg
A21360-5TTA-Q6 5mg
A21724-10TTA-Q6 (isomer) 10mg
A21724-100TTA-Q6 (isomer) 100mg

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