Apohyoscine | CAS:535-26-2 | Manufacturer ChemFaces

Apohyoscine

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Size /Price /Stock	10 mM * 1 mL in DMSO / Inquiry
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Apohyoscine Description

Source:	The aerial parts of Datura innoxia.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

Planta Medica, 1980,38(4):356-358.

Metabolism of hyoscine fed to the aerial parts of Solandra grandiflora.[Reference: WebLink]

METHODS AND RESULTS:
(-)-Hyoscine infiltrated into the aerial parts of S. grandiflora was transformed to ( plus or minus )-hyoscine, Apohyoscine, ( plus or minus )-norhyoscine, scopine and oscine.

Phytochemistry,1976,15(2): 287-9.

Biosynthesis of C6-C3 acids in Datura innoxia[Reference: WebLink]

METHODS AND RESULTS:
Datura innoxia plants were fed via the roots with cinnamic acid-[214C], (±)-phenyllactic (2-hydroxy-3-phenylpropanoic) acid-[214C] and phenylalanine-[2-14C]. In each case Apohyoscine, hyoscine, hyoscyamine and littorine were isolated from the aerial parts, and hyoscine, hyoscyamine and littorine from the roots. Cinnamic acid was not incorporated into the acid moieties of the alkaloids. Phenyllactic acid served as a better precursor than phenylalanine for tropic acid (hyoscine and hyoscyamine) and atropic acid (Apohyoscine).
CONCLUSIONS:
Phenylalanine served as an effective precursor for the phenyllactic acid moiety of Littorine.

Product Name	Apohyoscine
Price:
CAS No.:	535-26-2
Catalog No.:	CFN00150
Molecular Formula:	C₁₇H₁₉NO₃
Molecular Weight:	285.34 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:	The aerial parts of Datura innoxia.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Alkaloids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	3.5046 mL	17.523 mL	35.0459 mL	70.0918 mL	87.6148 mL
5 mM	0.7009 mL	3.5046 mL	7.0092 mL	14.0184 mL	17.523 mL
10 mM	0.3505 mL	1.7523 mL	3.5046 mL	7.0092 mL	8.7615 mL
50 mM	0.0701 mL	0.3505 mL	0.7009 mL	1.4018 mL	1.7523 mL
100 mM	0.035 mL	0.1752 mL	0.3505 mL	0.7009 mL	0.8761 mL

CFN00148	Anisodine	52646-92-1	319.36	C₁₇H₂₁NO₅
CFN00149	Apoatropine	500-55-0	271.36	C₁₇H₂₁NO₂
CFN00150	Apohyoscine	535-26-2	285.34	C₁₇H₁₉NO₃
CFN00151	Aponorhyoscine	25650-56-0	271.31	C₁₆H₁₇NO₃
CFN00171	Nortropacocaine	18470-33-2	231.29	C₁₄H₁₇NO₂
CFN00177	Bellendine	32152-73-1	205.26	C₁₂H₁₅NO₂
CFN00181	Brugine	14912-30-2	273.42	C₁₂H₁₉NO₂S₂
CFN00182	Chalcostrobamine	75638-72-1	269.34	C₁₇H₁₉NO₂
CFN00183	Cocaine	50-36-2	303.35	C₁₇H₂₁NO₄
CFN00184	Pseudococaine	478-73-9	303.35	C₁₇H₂₁NO₄