Synonym
BE-18591; BE 18591; BE18591
IUPAC/Chemical Name
(E)-N-((4'-methoxy-1H,5'H-[2,2'-bipyrrol]-5'-ylidene)methyl)dodecan-1-amine
InChi Key
FDQXCPYGFLFWFX-DYTRJAOYSA-N
InChi Code
InChI=1S/C22H35N3O/c1-3-4-5-6-7-8-9-10-11-12-15-23-18-21-22(26-2)17-20(25-21)19-14-13-16-24-19/h13-14,16-18,23-24H,3-12,15H2,1-2H3/b21-18+
SMILES Code
CCCCCCCCCCCCN/C=C(C(OC)=C1)/N=C1C2=CC=CN2
Appearance
To be determined
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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
Preparing Stock Solutions
The following data is based on the
product
molecular weight
357.54
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 |
1: Tanigaki K, Sato T, Tanaka Y, Ochi T, Nishikawa A, Nagai K, Kawashima H,
Ohkuma S. BE-18591 as a new H(+)/Cl(-) symport ionophore that inhibits
immunoproliferation and gastritis. FEBS Lett. 2002 Jul 31;524(1-3):37-42. doi:
10.1016/s0014-5793(02)02996-4. PMID: 12135738.
2: Grenade NL, Chiriac DS, Pasternak ARO, Babulic JL, Rowland BE, Howe GW, Ross
AC. Discovery of a Tambjamine Gene Cluster in Streptomyces Suggests
Convergent Evolution in Bipyrrole Natural Product Biosynthesis. ACS Chem Biol.
2023 Feb 17;18(2):223-229. doi: 10.1021/acschembio.2c00685. Epub 2023 Jan 4.
PMID: 36599132.
3: Pinkerton DM, Banwell MG, Willis AC. Total syntheses of tambjamines C, E, F,
G, H, I and J, BE-18591, and a related alkaloid from the marine bacterium
Pseudoalteromonas tunicata. Org Lett. 2007 Nov 22;9(24):5127-30. doi:
10.1021/ol7024313. Epub 2007 Oct 27. PMID: 17963401.
4: Pinkerton DM, Banwell MG, Garson MJ, Kumar N, de Moraes MO, Cavalcanti BC,
Barros FW, Pessoa C. Antimicrobial and cytotoxic activities of synthetically
derived tambjamines C and E - J, BE-18591, and a related alkaloid from the
marine bacterium Pseudoalteromonas tunicata. Chem Biodivers. 2010
May;7(5):1311-24. doi: 10.1002/cbdv.201000030. PMID: 20491087.
5: Kojiri K, Nakajima S, Suzuki H, Okura A, Suda H. A new antitumor substance,
BE-18591, produced by a streptomycete. I. Fermentation, isolation, physico-
chemical and biological properties. J Antibiot (Tokyo). 1993
Dec;46(12):1799-803. doi: 10.7164/antibiotics.46.1799. PMID: 8294236.
6: Nakajima S, Kojiri K, Suda H. A new antitumor substance, BE-18591, produced
by a streptomycete. II. Structure determination. J Antibiot (Tokyo). 1993
Dec;46(12):1894-6. doi: 10.7164/antibiotics.46.1894. PMID: 8294249.