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Vasicine

Vasicine Suppliers list
Company Name: Huzhou ZhanShu Biotechnology Co.,Ltd  Gold
Tel: 0572-8889530 18167260939
Email: zsubio@163.com
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
Email: sales@BioChemBest.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Sinopharm Chemical Reagent Co,Ltd.  
Tel: 86-21-63210123
Email: sj_scrc@sinopharm.com
Company Name: BioBioPha Co., Ltd.  
Tel: 0871-65217109
Email: y.liu@mail.biobiopha.com

Vasicine manufacturers

  • VASICINE
  • VASICINE pictures
  • $1080.00
  • 2024-04-02
  • CAS:6159-55-3
  • Min. Order: 1mg
  • Purity: 98
  • Supply Ability: 5 Kg
  • Vasicine
  • Vasicine pictures
  • 2023-02-24
  • CAS:6159-55-3
  • Min. Order: 5mg
  • Purity: ≥97%(HPLC)
  • Supply Ability: 10 g
Vasicine Basic information
Product Name:Vasicine
Synonyms:1-b)quinazolin-3-ol,1,2,3,9-tetrahydro-pyrrolo(;vasicin;AKOS NCG1-0080;VITAS-BB TBB000541;VASICINE;C10733;HARMALINE HCL(RG);(3R)-1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-3-ol
CAS:6159-55-3
MF:C11H12N2O
MW:188.23
EINECS:228-180-8
Product Categories:Miscellaneous Natural Products;Alkaloids
Mol File:6159-55-3.mol
Vasicine Structure
Vasicine Chemical Properties
Melting point 211.5°C
Boiling point 323.23°C (rough estimate)
density 1.1124 (rough estimate)
refractive index 1.5850 (estimate)
storage temp. 2-8°C
solubility DMSO : 83.33 mg/mL (442.70 mM; Need ultrasonic)
form Powder
pKa13.08±0.20(Predicted)
color White to off-white
Major Applicationpharmaceutical
InChIInChI=1S/C11H12N2O/c14-10-5-6-13-7-8-3-1-2-4-9(8)12-11(10)13/h1-4,10,14H,5-7H2/t10-/m0/s1
InChIKeyYIICVSCAKJMMDJ-JTQLQIEISA-N
SMILESN1C2=C(C=CC=C2)CN2CC[C@H](O)C=12
Safety Information
Hazard Codes Xn
Risk Statements 22
RIDADR 1544
WGK Germany WGK 3
HazardClass 6.1(b)
PackingGroup III
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
Vasicine Usage And Synthesis
DescriptionThis quinazoline alkaloid was first isolated from the leaves of Adhatoda vasica Nees by Hooper and subsequently discovered in Peganum harmala under the name Peganine. The base is optically inactive although Spath and Kesztler have reported the isolation of the (-)-form from the fresh leaves of A. vasica and Rosenfeld and Kolesnikow have obtained the same form from the flowers and stems of Peganum harmala. The salts are readily obtained crystalline, e.g. the hydrochloride dihydrate, m.p. 208°C (dry); hydriodide dihydrate, m.p. 195°C (dry); picrate, m.p. 199°C (dec.) and the methiodide, m.p. 187°C.
With AcOH, the alkaloid gives an anomalous acetyl derivative, m.p. 165°C, subsequently shown to be N-acetylpedadiene. Oxidation with KMn04 gives 4-quinazolone and 4-keto-3 :4-dihydroxyquinazolyl-3-acetic acid, the latter characterized as the methyl ester, m.p. 152°C.
The crude drug from A. vasica is used in India as a remedy for asthma while the pure alkaloid acts as a bronchodilator.
Chemical PropertiesWhite needle-like crystals, soluble in organic solvents such as methanol, ethanol, DMSO, etc., derived from camels.
UsesVasicine is used for content determination/identification/pharmacological experiments, etc.
Biological ActivityVasicine, isolated from A. vasica, is an alkaloid. It is a natural cholinesterase (cholinesterase) inhibitor, has anticholinesterase activity in preclinical models, and can be used for the development of therapeutic drugs for Alzheimer's disease.
targetAntifection | AChR
ReferencesHooper., Pharm. J., 18,841 (1888)
Sen, Ghose.,J. Ind. Chem. Soc., 1,315 (1924)
Ghose., ibid, 4, 1 (1927)
Spath, Nakawitz., Ber., 67,45 (1934)
Spath, Kuffner., ibid, 67, 1494 (1934)
Narang, Ray., Chem. & Ind., 53,698 (1934)
Hanford, Liang, Adams., J. Amer. Chem. Soc., 56, 2780 (1934)
Ghoseetal., ibid, 57,921,951 (1935)
Rosenfeld, Kolesnikov., Ber., 69, 2022 (1936)
Pharmacology: Chopra., Ind. Med. Gaz., 60, 354 (1925)
Tutaev, Makarova., Trans. Ukraine Inst. Exp. Pharm., 1,32 (1938)
Vasicine Preparation Products And Raw materials
Tag:Vasicine(6159-55-3) Related Product Information
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