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Cargutocin

Product Name
Cargutocin
CAS No.
33605-67-3
Chemical Name
Cargutocin
Synonyms
Y-5350;Statogin;Cargutocin;Cargutocin USP/EP/BP;1-Butyryl-7-glycyl-1,6-dicarbaoxytocin;Butyryl(1)-L-Tyr-L-Ile-L-Gln-L-Asn-L-Abu(1)-Gly-L-Leu-Gly-NH2;Glycinamide, L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-(2S)-7-carboxyheptanoylglycyl-L-leucyl-, (5→1)-lactam;(2S,5S,8S,11S)-5-[(2S)-butan-2-yl]-8-(2-carbamoylethyl)-11-(carbamoylmethyl)-N-[[(1S)-1-(carbamoylmethylcarbamoyl)-3-methyl-butyl]carbamoylmethyl]-2-[(4-hydroxyphenyl)methyl]-3,6,9,12,20-pentaoxo-1,4,7,10,13-pentazacycloicosane-14-carboxamide
CBNumber
CB11178220
Molecular Formula
C42H65N11O12
Formula Weight
916.041
MOL File
33605-67-3.mol
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Cargutocin Property

alpha 
D25 -44.0° (c = 0.55 in water)
Boiling point:
801.01°C (rough estimate)
Density 
1.1903 (rough estimate)
refractive index 
1.6500 (estimate)
CAS DataBase Reference
33605-67-3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0010942
Product name
CARGUTOCIN
Purity
95.00%
Packaging
5MG
Price
$505.15
Updated
2021/12/16
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Cargutocin Chemical Properties,Usage,Production

Originator

Statocin,Yoshitomi,Japan,1982

Definition

ChEBI: Cargutocin is an oligopeptide.

Manufacturing Process

To a suspension of Z-Tyr(Bz)-Ile-Gln-Asn-Asu(OTCP)-Gly-Leu-Gly-NH2 (1,310 mg) in DMF (350 ml) is added a suitable amount of palladium black. Hydrogen gas is introduced with stirring at room temperature (25°C) for about 40 hours. After stirring the mixture at 30°-35°C for several hours, the catalyst is filtered off and the filtrate is concentrated under reduced pressure. A large amount of ether is added to the residue, and the white coagulum is collected by filtration, washed with ether and dried. This is dissolved in water (30 ml), and the solution is filtered. The filtrate is passed through a column (3 x 11.5 cm) of Amerlite IR-45 (OH-form). The fractions which show a UV-absorption maximum at 280 nm are combined and passed through a column (3 x 125 cm) of CM-Sephadex C-25 to remove the noncyclic compound and obtain neutral parts. The detection of the objective compound is made by UV_x0002_absorption at 280 nm. The aqueous solution of the neutral parts is concentrated below 35°C, under reduced pressure, and the concentrate is lyophilized to give 504 mg of the crude title compound in the form of 5 hydrate.

Therapeutic Function

Oxytocic

Cargutocin Preparation Products And Raw materials

Raw materials

Preparation Products

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Cargutocin Suppliers

Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-89586680 +86-18192503167
Fax
+86-29-88380327
Email
1026@dideu.com
Country
China
ProdList
9231
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354
Email
support@targetmol.com
Country
United States
ProdList
19973
Advantage
58

33605-67-3, CargutocinRelated Search:


  • Cargutocin
  • 1-Butyryl-7-glycyl-1,6-dicarbaoxytocin
  • Butyryl(1)-L-Tyr-L-Ile-L-Gln-L-Asn-L-Abu(1)-Gly-L-Leu-Gly-NH2
  • Statogin
  • Y-5350
  • (2S,5S,8S,11S)-5-[(2S)-butan-2-yl]-8-(2-carbamoylethyl)-11-(carbamoylmethyl)-N-[[(1S)-1-(carbamoylmethylcarbamoyl)-3-methyl-butyl]carbamoylmethyl]-2-[(4-hydroxyphenyl)methyl]-3,6,9,12,20-pentaoxo-1,4,7,10,13-pentazacycloicosane-14-carboxamide
  • Glycinamide, L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-(2S)-7-carboxyheptanoylglycyl-L-leucyl-, (5→1)-lactam
  • Cargutocin USP/EP/BP
  • 33605-67-3
  • C42H65N11O12