VU 6008667

VU 6008667 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:VU 6008667
CAS:2092923-21-0
Purity:98.00% Package:1 mL * 10mM (in DMSO);10 mg;100 mg;200 mg;25 mg;5 mg;50 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Email: support@targetmol.com
Products Intro: Product Name:VU 6008667
CAS:2092923-21-0
Package:25mg;854USD|50mg;1110USD|100mg;1860USD
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:VU 6008667
CAS:2092923-21-0
Purity:99% Package:2mg;5mg;25mg
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com
Products Intro: Product Name:VU 6008667
CAS:2092923-21-0
Purity:97.0% Package:5mg
Company Name: BOC Sciences  
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Products Intro: Product Name:VU 6008667
CAS:2092923-21-0
Purity:99% Remarks:VU 6008667 is a selective negative allosteric modulator (NAM) of M5 muscarinic acetylcholine receptor (mAChR) (IC50 values of 1.2 and 1.6 μM in human and rat M5, respectively). Moreover, VU6008667 has

VU 6008667 manufacturers

  • VU 6008667
  • VU 6008667 pictures
  • $854.00 / 25mg
  • 2025-08-21
  • CAS:2092923-21-0
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  • Supply Ability: 10g
VU 6008667 Basic information
Product Name:VU 6008667
Synonyms:VU 6008667;5H-Imidazo[2,1-a]isoindol-5-one, 9b-(4-chloro-3-methylphenyl)-1-(3,4-difluorobenzoyl)-1,2,3,9b-tetrahydro-, (9bS)-
CAS:2092923-21-0
MF:C24H17ClF2N2O2
MW:438.85
EINECS:
Product Categories:
Mol File:2092923-21-0.mol
VU 6008667 Structure
VU 6008667 Chemical Properties
Boiling point 616.1±55.0 °C(Predicted)
density 1.48±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 100 mg/mL (227.87 mM)
pka-2.76±0.40(Predicted)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
VU 6008667 Usage And Synthesis
UsesVU 6008667 is a selective negative allosteric modulator of M5 NAM with IC50s of 1.2 μM and 1.6 μM for human M5 and rat M5, respectively. High CNS penetration[1].
in vivo

VU 6008667 (1 mg/kg)/PO (3 mg/kg, solution dose) displays a diminished elimination half-life (t1/2=2.3 hr) driven by a smaller volume (Vss=7.4 L/kg) and higher clearance (CLp=82 mL/min/kg), with moderate oral bioavailability (17% F)[1].

Animal Model:RAT (PK study)[1]
Dosage:1 mg/kg; 3 mg/kg
Administration:oral adminstration
Result:Had a desired short half-life in rat (t1/2= 2.3 hr), with moderate oral bioavailability (17% F).
IC 50mAChR5
References[1] McGowan KM et al, Continued optimization of the M5 NAM ML375: Discovery of VU6008667, an M5 NAM with high CNS penetration and a desired short half-life in rat for addiction studies. Bioorg Med Chem Lett. 2017 Mar 15;27(6):1356-1359. DOI:10.1016/j.bmcl.2017.02.020
VU 6008667 Preparation Products And Raw materials
Tag:VU 6008667(2092923-21-0) Related Product Information
N-(4-Methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide VU0134992(hydrochloride) VU6005649 VU 591 hydrochloride VU0810464 VU0483605 N-(4-Chloro-3-methoxyphenyl)-2-pyridinecarboxamide 1-(4-Methoxybenzyl)-5-trifluoromethoxyisatin (1R,2R)-N-([S]-1-{4-[5-broMo-2-oxo-2,3-dihydro-1H-benzo(d)iMidazol-1-yl]piperidin-1-yl}propan-2-yl)-2-phenylcyclopropanecarboxaMide 5-Amino-3,4-dimethyl-thieno[2,3-c]pyridazine-6-carboxylic acid 4-trifluoromethanesulfonyl-benzylamide 3-methylsulfanyl-7,8-dihydro-6H-cyclopenta[4,5]thieno[1,2-c]pyrimidin-1-amine VU 0360172 VU 0365114 VU 0357121 VU 0360223 VU 0364439 VU0650786 VU0661013

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