diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate
Calcium Ionophore I
CAS: 58801-34-6
Molecular Formula: C38H72N2O8
diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate - Names and Identifiers
| Name | Calcium Ionophore I |
| Synonyms | CA 1001 ETH 1001 CALCIUM IONOPHORE CALCIUM IONOPHORE I Calcium Ionophore I (-)-(R,R)-N,N'-BIS[11-(ETHOXYCARBONYL)UNDECYL]-N,N',4,5-TETRAMETHYL-3,5-DIOXAOCTANEDIAMIDE (-)-(R,R)-N,N'-BIS-[11-(ETHOXYCARBONYL)UNDECYL]-N,N'-4,5-TETRAMETHYL-3,6-DIOXAOCTANEDIAMIDE DIETHYL-N,N'-[(4R,5R)-4,5-DIMETHYL-1,8-DIOXO-3,6-DIOXAOCTAMETHYLENE]BIS(12-METHYLAMINODODECANOATE) diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate |
| CAS | 58801-34-6 |
| EINECS | 261-449-8 |
diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate - Physico-chemical Properties
| Molecular Formula | C38H72N2O8 |
| Molar Mass | 684.99 |
| Density | 1.000±0.06 g/cm3(Predicted) |
| Boling Point | 715.1±50.0 °C(Predicted) |
| Appearance | Light yellow, translucent, highly viscous oil |
| BRN | 2343275 |
| pKa | -0.52±0.70(Predicted) |
| Storage Condition | 2-8°C |
| Use | Calcium ionophore I is a Ca2+-selective ionophore for biological membranes that can be used in micro |
diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate - Risk and Safety
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 9-23 |
diethyl [R-(R*,R*)]-13,17,18,22-tetramethyl-14,21-dioxo-16,19-dioxa-13,22-diazatetratriacontanedioate - Introduction
Calcium Ionophore I, also known as A23187, is an organic compound with the chemical formula C29H37N3O6, which has the morphology of a white crystalline powder. It is a naturally occurring enzyme inhibitor.
The main use of Calcium Ionophore I is as a research tool, especially in the field of cell biology and molecular biology. It can be used to study the role of calcium ions in cell signal transduction, regulation of intracellular calcium homeostasis, and processes related to cell motility and differentiation. In addition, it can also be used to study the transport of charged ions and cell membrane permeability.
The common method for preparing Calcium Ionophore I is extraction from strains of the genus Streptomyces. In addition, there are synthetic methods that can be used to prepare the compounds.
When using Calcium Ionophore I, you need to pay attention to its safety. The compound is irritating to the skin and eyes and may cause allergic reactions. Wear appropriate personal protective equipment such as gloves and goggles during use. At the same time, it should be stored in a dry, cool place, avoid contact with oxygen and moisture. If inhaled or ingested, seek medical attention immediately.
The main use of Calcium Ionophore I is as a research tool, especially in the field of cell biology and molecular biology. It can be used to study the role of calcium ions in cell signal transduction, regulation of intracellular calcium homeostasis, and processes related to cell motility and differentiation. In addition, it can also be used to study the transport of charged ions and cell membrane permeability.
The common method for preparing Calcium Ionophore I is extraction from strains of the genus Streptomyces. In addition, there are synthetic methods that can be used to prepare the compounds.
When using Calcium Ionophore I, you need to pay attention to its safety. The compound is irritating to the skin and eyes and may cause allergic reactions. Wear appropriate personal protective equipment such as gloves and goggles during use. At the same time, it should be stored in a dry, cool place, avoid contact with oxygen and moisture. If inhaled or ingested, seek medical attention immediately.
Last Update：2024-04-10 22:29:15
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