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Sodium deoxyribose cytidylic acid

  • USD 1 - 100 / Gram  
  • 10 Gram/Grams
  • Pharmaceutical Grade
  • 3-5 days afer your payment
  • CAS 16789-98-3
  • Keep in cool dry and dark place
  • Tag:Desmopressin acetate
  • Supplier - Shenzhen Simeiquan BioChemical Tech Co.ltd
  • China (Mainland)China (Mainland)
  • US$10 Million - US$50 Million
  • Above 1000 People
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Post Date : August 01
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Item specifics

Pharmaceutical Grade
3-5 days afer your payment
CAS 16789-98-3
Keep in cool dry and dark place
Western Union, Money gram, T/T
DDAVP
Auxiliaries and Other Medicinal Chemicals
bella.lee36
C46H64N14O12S2
99%
China (Mainland),Hubei
White crystalline powder
Discreet Package as your requirement
smile2bella@ycphar.com
16789-98-3
Medicine Grade
YC

Specifications

CAS 16789-98-3 Desmopressin acetate/Sodium deoxyribose cytidylic acid

Polypeptide Hormones Desmopressin Acetate CAS 16789-98-3 For Coagulation Zdisorders & Diabetes Insipidus

Desmopressin Acetate

Alias : Sodium deoxyribose cytidylic acid,DDAVP

Cas No. : 16789-98-3

Molecular Formula : C46H64N14O12S2

Molecular Weight :1189.32

Purity (HPLC) : 98.0%min.

Appearance : White powder

Single Impurity (HPLC) : 0.5%max

Amino Acid Composition : ±10% of theoretical

Peptide Content (N%) : ≥80.0%

Water Content (Karl Fischer) : ≤8.0%

Acetate Content (HPIC) : ≤12.0%

MS (ESI) : Consistent

Mass Balance : 95.0~105.0%

Grade : Pharmaceutical Grade

Storage: Closed, below 2 ~ 8°C preservation

Usage : Desmopressin Acetate is used for nocturnal enuresis, coagulation zdisorders and diabetes insipidus.

Description:

Desmopressin (trade names: DDAVP, DesmoMelt, Minirin, Minirin Melt, Octim, Stimate) is a synthetic replacement for vasopressin, the hormone that reduces urine production. It may be taken nasally, intravenously, or as an oral or sublingual tablet. Physicians prescribe desmopressin most frequently for treatment of diabetes insipidus, bedwetting, or nocturia.

Application :

Doctors prescribe desmopressin frequently for treatment of nocturnal enuresis (bedwetting). It is usually prescribed in the form of oral desmopressin acetate, DDAVP. Patients taking DDAVP are 4.5 times more likely to sleep without disruption compared with placebo.

Desmopressin can be used to promote the release of von Willebrand factor (with subsequent increase in factor VIII survival secondary to vWF complexing) in patients with coagulation disorders such as von Willebrand disease, mild hemophilia A (factor VIII deficiency), and thrombocytopenia. It can be used with uremic induced platelet dysfunction. It is not effective in the treatment of hemophilia B (factor IX deficiency), severe hemophilia A, or von Willebrand 2B.

Desmopressin is used in the treatment of central diabetes insipidus (DI), to replace endogenous ADH that is missing in the central nervous system type of this disorder (decreased production of ADH from the posterior pituitary). It is also used in the diagnostic workup for diabetes insipidus, in order to distinguish central from nephrogenic DI.

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Desmopressin acetate

Desmopressin acetate

Desmopressin acetate

CAS 16789-98-3 Desmopressin acetate

Polypeptide Hormones Desmopressin Acetate CAS 16789-98-3 For Coagulation Zdisorders & Diabetes Insipidus

Desmopressin Acetate

Alias : Sodium deoxyribose cytidylic acid,DDAVP

Cas No. : 16789-98-3

Molecular Formula : C46H64N14O12S2

Molecular Weight :1189.32

Purity (HPLC) : 98.0%min.

Appearance : White powder

Single Impurity (HPLC) : 0.5%max

Amino Acid Composition : ±10% of theoretical

Peptide Content (N%) : ≥80.0%

Water Content (Karl Fischer) : ≤8.0%

Acetate Content (HPIC) : ≤12.0%

MS (ESI) : Consistent

Mass Balance : 95.0~105.0%

Grade : Pharmaceutical Grade

Storage: Closed, below 2 ~ 8°C preservation

Usage : Desmopressin Acetate is used for nocturnal enuresis, coagulation zdisorders and diabetes insipidus.

Description:

Desmopressin (trade names: DDAVP, DesmoMelt, Minirin, Minirin Melt, Octim, Stimate) is a synthetic replacement for vasopressin, the hormone that reduces urine production. It may be taken nasally, intravenously, or as an oral or sublingual tablet. Physicians prescribe desmopressin most frequently for treatment of diabetes insipidus, bedwetting, or nocturia.

Application :

Doctors prescribe desmopressin frequently for treatment of nocturnal enuresis (bedwetting). It is usually prescribed in the form of oral desmopressin acetate, DDAVP. Patients taking DDAVP are 4.5 times more likely to sleep without disruption compared with placebo.

Desmopressin can be used to promote the release of von Willebrand factor (with subsequent increase in factor VIII survival secondary to vWF complexing) in patients with coagulation disorders such as von Willebrand disease, mild hemophilia A (factor VIII deficiency), and thrombocytopenia. It can be used with uremic induced platelet dysfunction. It is not effective in the treatment of hemophilia B (factor IX deficiency), severe hemophilia A, or von Willebrand 2B.

Desmopressin is used in the treatment of central diabetes insipidus (DI), to replace endogenous ADH that is missing in the central nervous system type of this disorder (decreased production of ADH from the posterior pituitary). It is also used in the diagnostic workup for diabetes insipidus, in order to distinguish central from nephrogenic DI.

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Deslorelin acetate

Deslorelin acetate

Deslorelin acetate

CAS 57773-65-6 Deslorelin acetate

99% Polypeptide Hormones Deslorelin AcetateCAS 57773-65-6 For The Initial Flare Effect Upon The Pituitary

Deslorelin Acetate

Sequence : Glp-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-Pro-NHEt

Cas No. : 57773-65-6

Molecular Formula : C64H83N17O12

Molecular Weight : 1282.47

Purity (HPLC) : 99.0%min.

Appearance : White powder

Single Impurity (HPLC) : 0.5%max

Amino Acid Composition : ±10% of theoretical

Peptide Content (N%) : ≥80.0%

Water Content (Karl Fischer) : ≤8.0%

Acetate Content (HPIC) : ≤12.0%

MS (ESI) : Consistent

Mass Balance : 95.0~105.0%

Grade : Pharmaceutical Grade

Storage: Closed, below 2 ~ 8°C preservation

Usage : Deslorelin is primarily used for the initial flare effect upon the pituitary, and its associated surge of LH secretion.

Deslorelin acetate is an injectable gonadotropin releasing hormone super-agonist (GnRH agonist) also known as an LHRH agonist. It stops the production of sex hormones (testosterone and oestrogen).

Deslorelin Acetate is marketed by Peptech with the brand name Ovuplant. It is currently approved for use in veterinary medicine and is used to induce ovulation in mares as part of the artificial insemination process. It is also used to stabilize high-risk pregnancies, mainly of livestock. Unlike other GnRH agonists, which are mainly used to inhibit luteinizing hormone and follicle-stimulating hormone by their ultimate downregulation of the pituitary gland, Deslorelin is primarily used for the initial flare effect upon the pituitary, and its associated surge of LH secretion.

Application:

Deslorelin was successfully trialed in the US and was approved for veterinary use under certain circumstances. In Europe, it was approved for use in equine assisted reproduction.

It is also being trialed in humans to study its efficacy in treatment of breast cancer in women,and in treating precocious puberty and congenital adrenal hyperplasia in male and female children.

Detail more >>
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