WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H319598
CAS#: 476333-91-2 (HCl)
Description: Ritobegron, also known as KUC-7483, is a potent and selective β3-adrenoceptor agonist. Ritobegron displayed potent and selective β(3)-AR agonistic activity toward transfected human β-AR and exhibited a high selectivity for the bladder versus other organs in rats. Ritobegron decreased intravesical pressure with minimal effects on the cardiovascular system in anesthetized rats. Ritobegron shows promise as a potential agent for the treatment of overactive bladder.
Hodoodo Cat#: H319598
Name: Ritobegron HCl
CAS#: 476333-91-2 (HCl)
Chemical Formula: C23H32ClNO5
Exact Mass: 0.00
Molecular Weight: 437.961
Elemental Analysis: C, 63.08; H, 7.37; Cl, 8.09; N, 3.20; O, 18.27
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Related CAS #: 476333-91-2 (HCl) 255733-81-4 (free base)
Synonym: KUC-7483; KUC 7483; KUC7483; Ritobegron; Ritobegron HCl; Ritobegron hydrochloride; brand name: Myrbetriq.
IUPAC/Chemical Name: ethyl 2-(4-(2-(((1R,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl)amino)ethyl)-2,5-dimethylphenoxy)acetate hydrochloride
InChi Key: SDZAMDXEQUMDBE-DQFHVVJASA-N
InChi Code: InChI=1S/C23H31NO5.ClH/c1-5-28-22(26)14-29-21-13-15(2)19(12-16(21)3)10-11-24-17(4)23(27)18-6-8-20(25)9-7-18;/h6-9,12-13,17,23-25,27H,5,10-11,14H2,1-4H3;1H/t17-,23-;/m0./s1
SMILES Code: O=C(OCC)COC1=CC(C)=C(CCN[C@@H](C)[C@H](O)C2=CC=C(O)C=C2)C=C1C.[H]Cl
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO, not in water
Shelf Life: >2 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
More Info:
Biological target: | |
In vitro activity: | |
In vivo activity: |
The following data is based on the product molecular weight 437.96 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
Formulation protocol: | |
In vitro protocol: | |
In vivo protocol: |
1: Abe Y, Ota E, Endo T, Murakami M, Kobayashi M. Absorption, disposition,
metabolism, and excretion of ritobegron (KUC-7483), a novel selective
β3-adrenoceptor agonist, in rats. Pharmazie. 2014 Dec;69(12):881-8. PubMed PMID:
25951660.
2: Maruyama I, Goi Y, Tatemichi S, Maruyama K, Hoyano Y, Yamazaki Y, Kusama H.
Bladder selectivity of the novel β₃-agonist ritobegron (KUC-7483) explored by in
vitro and in vivo studies in the rat. Naunyn Schmiedebergs Arch Pharmacol. 2012
Aug;385(8):845-52. doi: 10.1007/s00210-012-0755-x. Epub 2012 May 3. PubMed PMID:
22552730.
3: Maruyama I, Tatemichi S, Goi Y, Maruyama K, Hoyano Y, Yamazaki Y, Kusama H.
Effects of ritobegron (KUC-7483), a novel selective β3-adrenoceptor agonist, on
bladder function in cynomolgus monkey. J Pharmacol Exp Ther. 2012
Jul;342(1):163-8. doi: 10.1124/jpet.112.191783. Epub 2012 Apr 16. PubMed PMID:
22511202.
4: Maruyama I, Yonekubo S, Tatemichi S, Maruyama K, Hoyano Y, Yamazaki Y, Kusama
H. Effects of ritobegron (KUC-7483), a novel β3-adrenoceptor agonist, on both rat
bladder function following partial bladder outlet obstruction and on rat salivary
secretion: a comparison with the effects of tolterodine. J Smooth Muscle Res.
2012;48(5-6):115-24. PubMed PMID: 23538508.