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MedKoo Cat#: 584162 | Name: BFE-55

Description:

WARNING: This product is for research use only, not for human or veterinary use.

BFE-55 is derivative of befunolol (a beta-adrenergic partial agonist). BFE-55 interacts with only the high affinity sites in beta-adrenoceptors

Chemical Structure

BFE-55
BFE-55
CAS#21151-91-7

Theoretical Analysis

MedKoo Cat#: 584162

Name: BFE-55

CAS#: 21151-91-7

Chemical Formula: C14H19NO3

Exact Mass: 249.1365

Molecular Weight: 249.31

Elemental Analysis: C, 67.45; H, 7.68; N, 5.62; O, 19.25

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
BFE-55; BFE55; BFE 55.
IUPAC/Chemical Name
2-Propanol, 1-(7-benzofuranyloxy)-3-((1-methylethyl)amino)-
InChi Key
JSBPDRDKVNCRIK-UHFFFAOYSA-N
InChi Code
InChI=1S/C14H19NO3/c1-10(2)15-8-12(16)9-18-13-5-3-4-11-6-7-17-14(11)13/h3-7,10,12,15-16H,8-9H2,1-2H3
SMILES Code
OC(CNC(C)C)COC1=C(OC=C2)C2=CC=C1
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
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

Preparing Stock Solutions

The following data is based on the product molecular weight 249.31 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.

Recalculate based on batch purity %
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
1: Takayanagi I, Ogishima M, Koike K, Hisayama T, Hayashida M, Fujii M. Dose difference in beta-adrenergic blockers with intrinsic sympathomimetic action to block beta-adrenoceptors and induce sympathomimetic action. Gen Pharmacol. 1989;20(4):417-9. PubMed PMID: 2568966. 2: Takayanagi I, Koike K, Ogishima M, Hayashida M, Fujii M. Effect of histamine on two different affinity sites in beta-adrenoceptors. Gen Pharmacol. 1989;20(2):219-22. PubMed PMID: 2565848. 3: Koike K, Nakagoshi A, Takayanagi I. A derivative of befunolol, BFE-55, interacts with only the high affinity sites in beta-adrenoceptors. Can J Physiol Pharmacol. 1987 Oct;65(10):2150-3. PubMed PMID: 2827874. 4: Koike K, Takayanagi I. Interactions of befunolol, a beta-adrenergic partial agonist, and its derivatives with high and low affinity sites in beta-adrenoceptors. J Pharmacobiodyn. 1987 Sep;10(9):494-8. PubMed PMID: 2893834. 5: Takayanagi I, Koike K, Nakagoshi A. Interactions of some partial agonists with high and low affinity binding sites in beta-adrenoceptors. Can J Physiol Pharmacol. 1987 Jan;65(1):18-22. PubMed PMID: 2882827.