This is a demo store. No orders will be fulfilled.

Valbenazine tosylate - 10mM in DMSO, high purity , CAS No.1639208-54-0, Synaptic vesicular amine transporter inhibitor

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
V422021
Grouped product items
SKU Size
Availability
Price Qty
V422021-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$290.90

VMAT Inhibitors

Basic Description

Synonyms Valbenazine tosylate | Valbenazine ditosylate | 1639208-54-0 | NBI-98854 ditosylate | Valbenazine tosilate | 5SML1T733B | Valbenazine (tosylate) | UNII-5SML1T733B | Valbenazine tosylate [USAN] | 1639208-54-0 (tosylayte) | Valbenazine tosilate (JAN) | Valbenazine tosylate (USAN
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Valbenazine tosylate (NBI-98854) is the tosylate salt of valbenazine, a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki value of 150 nM while displaying no significant binding to VAMT1(Ki<10 μM).
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type INHIBITOR
Mechanism of action Synaptic vesicular amine transporter inhibitor
Product Description

Information

Valbenazine tosylate Valbenazine tosylate (NBI-98854) is the tosylate salt of valbenazine, a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki value of 150 nM while displaying no significant binding to VAMT1(Ki<10 μM).

Targets

VMAT2 150 nM(Ki)

In vitro

Valbenazine is a potent, selective, and specific inhibitor of VMAT2 with no inhibition of the related VMAT1 transporter and minimal off-target interactions at more than 80 other receptor transporters and ion channels.

In vivo

Valbenazine is a novel and highly selective VMAT2 inhibitor that is rapidly absorbed but more slowly metabolized, with a half-life of approximately 20 h that supports once-daily dosing. Valbenazine has moderate absorption with an absolute oral bioavailability of approximately 49%; time to maximum concentration ranges from 0.5 to 1.0 hour. Valbenazine can be taken with or without food. Valbenazine exhibits protein binding of 99%. Valbenazine is primarily metabolized via the hydrolysis of the valine ester and cytochrome P450 (CYP) 3A4/5 into R,R,R-HTBZ and a mono-oxy metabolite.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent Alpha amino acid esters
Alternative Parents Valine and derivatives  p-Methylbenzenesulfonates  Tosyl compounds  Tetrahydroisoquinolines  1-sulfo,2-unsubstituted aromatic compounds  Benzenesulfonyl compounds  Anisoles  Alkyl aryl ethers  Aralkylamines  Fatty acid esters  Piperidines  Sulfonyls  Organosulfonic acids  Carboxylic acid esters  Trialkylamines  Monocarboxylic acids and derivatives  Azacyclic compounds  Carbonyl compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  
Molecular Framework Not available
Substituents Alpha-amino acid ester - Valine or derivatives - P-methylbenzenesulfonate - Tetrahydroisoquinoline - Tosyl compound - Benzenesulfonate - Benzenesulfonyl group - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Anisole - Phenol ether - Alkyl aryl ether - Fatty acid ester - Aralkylamine - Toluene - Monocyclic benzene moiety - Fatty acyl - Piperidine - Benzenoid - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Organoheterocyclic compound - Ether - Azacycle - Monocarboxylic acid or derivatives - Primary amine - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Organic oxide - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
External Descriptors Not available

Product Properties

ALogP 7.062
HBD Count 1
Rotatable Bond 10

Names and Identifiers

IUPAC Name [(2R,3R,11bR)-9,10-dimethoxy-3-(2-methylpropyl)-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl] (2S)-2-amino-3-methylbutanoate;4-methylbenzenesulfonic acid
INCHI InChI=1S/C24H38N2O4.2C7H8O3S/c1-14(2)9-17-13-26-8-7-16-10-21(28-5)22(29-6)11-18(16)19(26)12-20(17)30-24(27)23(25)15(3)4;2*1-6-2-4-7(5-3-6)11(8,9)10/h10-11,14-15,17,19-20,23H,7-9,12-13,25H2,1-6H3;2*2-5H,1H3,(H,8,9,10)/t17-,19-,20-,23+;;/m1../s1
InChIKey BXGKAGLZHGYAMW-TZYFFPFWSA-N
Smiles CC1=CC=C(C=C1)S(=O)(=O)O.CC1=CC=C(C=C1)S(=O)(=O)O.CC(C)CC1CN2CCC3=CC(=C(C=C3C2CC1OC(=O)C(C(C)C)N)OC)OC
Isomeric SMILES CC1=CC=C(C=C1)S(=O)(=O)O.CC1=CC=C(C=C1)S(=O)(=O)O.CC(C)C[C@@H]1CN2CCC3=CC(=C(C=C3[C@H]2C[C@H]1OC(=O)[C@H](C(C)C)N)OC)OC
PubChem CID 92042922
Molecular Weight 762.97

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility 100
DMSO(mM) Max Solubility 131.066278172238
Water(mg / mL) Max Solubility -1
Water(mM) Max Solubility -1.31066278172238
Molecular Weight 763.000 g/mol
XLogP3
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 12
Rotatable Bond Count 10
Exact Mass 762.322 Da
Monoisotopic Mass 762.322 Da
Topological Polar Surface Area 200.000 Ų
Heavy Atom Count 52
Formal Charge 0
Complexity 776.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 4
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 3

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.