Capromorelin Tartrate
CAS No. 193273-69-7
Capromorelin Tartrate( CP 424391-18 )
Catalog No. M23880 CAS No. 193273-69-7
Capromorelin Tartrate is a potent, orally active growth hormone secretagogue receptor (GHSR) agonist (Ki: 7 nM for hGHS-R1a).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 46 | In Stock |
|
| 5MG | 31 | In Stock |
|
| 10MG | 55 | In Stock |
|
| 25MG | 122 | In Stock |
|
| 50MG | 210 | In Stock |
|
| 100MG | 312 | In Stock |
|
| 200MG | 445 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCapromorelin Tartrate
-
NoteResearch use only, not for human use.
-
Brief DescriptionCapromorelin Tartrate is a potent, orally active growth hormone secretagogue receptor (GHSR) agonist (Ki: 7 nM for hGHS-R1a).
-
DescriptionCapromorelin Tartrate is a potent, orally active growth hormone secretagogue receptor (GHSR) agonist (Ki: 7 nM for hGHS-R1a).(In Vitro):Capromorelin stimulates GH release in rat pituitary cell cultures with EC50 of 3 nM.(In Vivo):Dogs receiving capromorelin (30 mg/mL) have food consumption that is significantly greater than dogs treated with placebo. All dogs in the capromorelin group gain weight by 0.52 kg, more than that of placebo group. Capromorelin shows enhanced intestinal absorption in rodent models and exhibits superior pharmacokinetic properties, including high bioavailabilities in two animal species [F(rat)=65%, F(dog)=44%]. Capromorelin stimulates GH release in anesthesized rat model, with ED50 of 0.05 mg/kg iv.
-
In VitroCapromorelin stimulates GH release in rat pituitary cell cultures with EC50 of 3 nM.
-
In VivoDogs receiving capromorelin (30 mg/mL) have food consumption that is significantly greater than dogs treated with placebo. All dogs in the capromorelin group gain weight by 0.52 kg, more than that of placebo group. Capromorelin shows enhanced intestinal absorption in rodent models and exhibits superior pharmacokinetic properties, including high bioavailabilities in two animal species [F(rat)=65%, F(dog)=44%]. Capromorelin stimulates GH release in anesthesized rat model, with ED50 of 0.05 mg/kg iv.
-
SynonymsCP 424391-18
-
PathwayGPCR/G Protein
-
TargetGHSR
-
RecptorhGHS-R1a
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number193273-69-7
-
Formula Weight655.7
-
Molecular FormulaC32H40N5O10
-
Purity>98% (HPLC)
-
SolubilityDMSO:100 mg/mL (152.51 mM)
-
SMILESO=C([C@@H]([C@@H](O)C(O)=O)O)O.CC(C)(N)C(N[C@H](COCC1=CC=CC=C1)C(N(C[C@]23CC4=CC=CC=C4)CCC2=NN(C)C3=O)=O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Carpino PA, et al. Pyrazolinone-piperidine dipeptide growth hormone secretagogues (GHSs). Discovery of capromorelin. Bioorg Med Chem. 2003 Feb 20;11(4):581-90.
molnova catalog
related products
-
Anamorelin
A non-peptide, centrally-penetrant and selective agonist of GHSR with appetite-enhancing and anabolic effects.
-
GHRP-6 acetate
GHRP-6 acetate is a synthetic growth hormone (GH) secretagogue and an agonist of the GH secretagogue receptor (GHS-R) which is also known as the ghrelin receptor.
-
TAPI-1
TAPI-1, an ADAM17/TACE inhibitor, inhibits shedding of cytokine receptors.
Cart
sales@molnova.com