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PERUVOSIDE

CAS No.
1182-87-2
Chemical Name:
PERUVOSIDE
Synonyms
Enordin;encordin;Pervoside;peruvosid;PERUVOSIDE;(22)-enolide;PERUVOSIDE(RG);Peruvoside (90%);PERUVOSIDE USP/EP/BP;cannogeninthevetoside
CBNumber:
CB0266619
Molecular Formula:
C30H44O9
Molecular Weight:
548.66
MDL Number:
MFCD00133752
MOL File:
1182-87-2.mol
Last updated:2024-11-19 23:02:33

PERUVOSIDE Properties

Melting point 161-164°C
alpha D22 -71.7° (c = 1.54 in methanol)
Boiling point 540.83°C (rough estimate)
Density 1.1277 (rough estimate)
refractive index 1.5500 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka 12.92±0.70(Predicted)
form powder
color light yellow
FDA UNII CT36KGC6A6
ATC code C01AX02

SAFETY

Risk and Safety Statements

Hazard Codes  T
Risk Statements  23/24/25
Safety Statements  36/37/39-45
WGK Germany  3
RTECS  FH4915000
Toxicity cat,LD50,intravenous,145ug/kg (0.145mg/kg),GASTROINTESTINAL: NAUSEA OR VOMITINGCARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION)CARDIAC: CHANGE IN RATE,Archives Internationales de Pharmacodynamie et de Therapie. Vol. 126, Pg. 412, 1960.

PERUVOSIDE price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC P227570 Peruvoside(90%) 1182-87-2 25mg $380 2021-12-16 Buy
Biosynth Carbosynth FD146105 Peruvoside 1182-87-2 1mg $150 2021-12-16 Buy
Biosynth Carbosynth FD146105 Peruvoside 1182-87-2 2mg $260 2021-12-16 Buy
Biosynth Carbosynth FD146105 Peruvoside 1182-87-2 5mg $350 2021-12-16 Buy
Biosynth Carbosynth FD146105 Peruvoside 1182-87-2 10mg $500 2021-12-16 Buy
Product number Packaging Price Buy
P227570 25mg $380 Buy
FD146105 1mg $150 Buy
FD146105 2mg $260 Buy
FD146105 5mg $350 Buy
FD146105 10mg $500 Buy

PERUVOSIDE Chemical Properties,Uses,Production

Originator

Peruvoside ,Indena

Uses

Peruvoside is a cardiac glycoside with the same inotropic and chronotropic effects on heart function as Ouabain (O714500).

Definition

ChEBI: Peruvoside is a cardenolide glycoside.

Manufacturing Process

Peruvoside is obtained employing the fruit or seeds of ApocynaceaThevetia peruviana by the fermentation and the separation the extracted glucoside mixture by chromatography.
Two kilograms of the ground fruit of ApocynaceaThevetia peruviana is mixed with 100 g of grain chaff and moistened with 900 ml of hot water (approximately 60°C). The mixture is mixed with 20 ml of toluene and maintained at 45°-55°C in a closed vessel for 5 days. The thus fermented material is extracted six times with 1200 ml portions of acetone. The combined extracts are concentrated at 30°C under reduced pressure, until there remains about 600 ml of a dark colored aqueous concentrate. The latter is shaken out with an equal volume of petroleum ether. The organic phase is discarded after recovering the petroleum ether. The thus degreased aqueous concentrate is extracted six times with 500 ml portions of dichloromethane. The dichloromethane extracts are dried over sodium sulfate, combined, and concentrated to about 100 ml. Then the residue is stirred into 250 ml of petroleum ether. After standing overnight, the thus-separated crystallized product is vacuum-filtered, washed petroleum ether and dried at about 40°C. The thus obtained crude glycoside mixture (21 g) is dissolved in a mixture of chloroform/methanol and chromatographed on a column of silica gel. There is thus isolated a small amount of oil and fat, a total of 15.5 g of cerberine, acetylperuvoside and neriifolin, 2.2 g of pure peruvoside, MP: 160°-163°C; [α]22d=70° (c = 1.3 in CH3OH), corresponding to a yield 0.11%, based on the quantity of fruit of Thevetia peruviana employed as the starting material.
One kilogram of ground seeds of Thevetia peruviana is mixed with 300 g of grain chaff and moistened with 500 ml of hot water (60°C). After addition of 10 ml of toluene the mixture is allowed to stand in a sealed vessel for 5 days at 45°-55°C. Thereafter, the moist drug material is extracted six times with 500 ml portions of methanol. The extracts are concentrated at about 30°C to about 300 ml. Without degreasing, glycosides are extracted from this aqueous concentrate with three 300 ml portions followed by three 100 ml portions of chloroform. The chloroform extracts are concentrated at about 40°C to a volume of about 200 ml. This concentrate is then mixed with 500 ml of petroleum ether. After standing overnight, the crystallized product, which separated, is vacuum-filtered, washed with petroleum ether, and dried at 40°C. Yield of rude glycoside: 46.9 g. From this product, after the usual separation by chromatography, 5.1 g of pure peruvoside is obtained, MP: 161°-164°C. Yield 0.51%, based on the weight of the non-degreased seeds of Thevetia peruviana.

Therapeutic Function

Cardiotonic

Enzyme inhibitor

This cardiotonic glycoside or cardenoide (FW = 548.67 g/mol; CAS 1182- 87-2), named systematically as (3b,5b)-3-(6-deoxy-3-O-methyl-a-Lglucopyranosyl)oxyl-14-hydroxy-19-oxocard-20(22)-enolide, a component of neriperside from Thevetia neriifolia (yellow oleander) resembles oubain in its inotropic (force of contraction) and chronotropic (rate of contraction) effects on heart function. Orally administered peruvoside is effective in treating congestive heart failure. Note the structural similarities of the aglycon to digitoxigenin. Target(s): Na+ /K+ -exchanging ATPase.

PERUVOSIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 57)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 997 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897 sales@biopurify.com China 3772 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 22784 58
TargetMol Chemicals Inc.
support@targetmol.com United States 38631 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152 Mandy@hangyubiotech.com China 10986 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43340 58
Mensura Group Limited
+8618109034517 hkd008@vacorda.com China 2900 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 021-61259108 18621169109 market03@meryer.com China 40228 62
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32321 50

View Lastest Price from PERUVOSIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Peruvoside pictures 2024-11-19 Peruvoside
1182-87-2
US $328.00-778.00 / mg 10g TargetMol Chemicals Inc.
PERUVOSIDE pictures 2024-04-12 PERUVOSIDE
1182-87-2
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
  • Peruvoside pictures
  • Peruvoside
    1182-87-2
  • US $328.00-778.00 / mg
  • TargetMol Chemicals Inc.
  • PERUVOSIDE pictures
  • PERUVOSIDE
    1182-87-2
  • US $0.00 / kg
  • 99%
  • Shaanxi Haibo Biotechnology Co., Ltd
PERUVOSIDE (22)-enolide (3β,5β)-3-(6-Deoxy-3-O-methyl-α-L-glucopyranosyl]oxyl)-14-hydroxy-19-oxocard-20(22)-enolide 3β-[(6-Deoxy-3-O-methyl-α-L-glucopyranosyl)oxy]-14-hydroxy-19-oxo-5β,14β-card-20(22)-enolide Cannogenin α-L-thevetoside Enordin Pervoside (3β,5β)-3-[(6-Deoxy-3-O-Methyl-α-L-glucopyranosyl)oxy]-14-hydroxy-19-oxocard-20(22)-enolide Peruvoside (90%) (3beta,5beta)-3-[(6-deoxy-3-O-methyl-alpha-L\-glucopyranosyl)oxy]-14-hydroxy-19-oxocard-20(22)-enolide PERUVOSIDE FROM THEVETIA NERIIFOLIA PERUVOSIDE(RG) (3-beta,5-beta)-oxy-19-oxo 3-((6-deoxy-3-o-methyl-alpha-l-glucopyranosyl)oxy)-14-hydroxy-19-oxo-card-20 cannogeninalpha-l-thevetoside cannogeninthevetoside card-20(22)-enolide,3-((6-deoxy-3-o-methyl-alpha-l-glucopyranosyl)oxy)-14-hydr encordin peruvosid CANNOGENNIN-ALPHA-L-THEVETOSIDE [3BETA,5BETA]-3-[6-DEOXY-3-O-METHYL-ALPHA-L-GLUCOPYRANOSYL)OXYL]-14-HYDROXY-19-OXOCARD-20[22]-ENOLIDE PERUVOSIDE USP/EP/BP (3S,5R,8R,9S,10R,13R,14S,17R)-3-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde Card-20(22)-enolide, 3-[(6-deoxy-3-O-methyl-α-L-glucopyranosyl)oxy]-14-hydroxy-19-oxo-, (3β,5β)- 1182-87-2 C30H44O9