MedKoo Cat#: 584291 | Name: BU-E 75

Description:

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

BU-E 75 is a histamine H2 agonist.

Chemical Structure

BU-E 75
BU-E 75
CAS#114667-74-2

Theoretical Analysis

MedKoo Cat#: 584291

Name: BU-E 75

CAS#: 114667-74-2

Chemical Formula: C21H24F2N6

Exact Mass: 398.2031

Molecular Weight: 398.46

Elemental Analysis: C, 63.30; H, 6.07; F, 9.54; N, 21.09

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
BU-E 75; BU E 75
IUPAC/Chemical Name
Guanidine, N-(3-(3,4-difluorophenyl)-3-(2-pyridinyl)propyl)-N'-(3-(1H-imidazol-4-yl)propyl)-
InChi Key
ZHUPJEZTXBUHGR-UHFFFAOYSA-N
InChi Code
InChI=1S/C21H24F2N6/c22-18-7-6-15(12-19(18)23)17(20-5-1-2-9-26-20)8-11-28-21(24)27-10-3-4-16-13-25-14-29-16/h1-2,5-7,9,12-14,17H,3-4,8,10-11H2,(H,25,29)(H3,24,27,28)
SMILES Code
N=C(NCCCC1=CNC=N1)NCCC(C2=CC=C(F)C(F)=C2)C3=NC=CC=C3
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 398.46 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: Felix SB, Buschauer A, Baumann G. Therapeutic value of H2-receptor stimulation in congestive heart failure. Hemodynamic effects of BU-E-76, BU-E-75 and arpromidine (BU-E-50) in comparison to impromidine. Agents Actions Suppl. 1991;33:257-69. PubMed PMID: 1828932. 2: Buschauer A, Baumann G. Structure-activity relationships of histamine H2-agonists, a new class of positive inotropic drugs. Agents Actions Suppl. 1991;33:231-56. PubMed PMID: 1828931. 3: Rixen D, Neugebauer E, Lechleuthner A, Buschauer A, Nagelschmidt M, Thoma S, Rink A. Beneficial effect of H2-agonism and H1-antagonism in rat endotoxic shock. Shock. 1994 Jul;2(1):47-52. PubMed PMID: 7735983. 4: Bungardt E, Buschauer A, Moser U, Schunack W, Lambrecht G, Mutschler E. Histamine H1 receptors mediate vasodilation in guinea-pig ileum resistance vessels: characterization with computer-assisted videomicroscopy and new selective agonists. Eur J Pharmacol. 1992 Oct 6;221(1):91-8. PubMed PMID: 1459193. 5: Lemos Legnazzi B, Shayo C, Monczor F, Martin ME, Fernandez N, Brodsky A, Baldi A, Davio C. Rapid desensitization and slow recovery of the cyclic AMP response mediated by histamine H(2) receptors in the U937 cell line. Biochem Pharmacol. 2000 Jul 15;60(2):159-66. PubMed PMID: 10825460. 6: Kleine-Tebbe J, Buschauer A, Friese A, Schunack W, Kunkel G. Modulation of IgE-mediated histamine release from human leukocytes by a new class of histamine H2-agonists. Agents Actions. 1992 Mar;35(3-4):185-91. PubMed PMID: 1382368. 7: Monczor F, Legnazzi BL, Rivera E, Davio C. Tiotidine, a classical H2-antagonist, presents characteristics of an inverse agonist in U937 cell line. Inflamm Res. 1998;47 Suppl 1:S42-3. PubMed PMID: 9561408.