(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid
15-ketoprostaglandin F2A
CAS: 35850-13-6
Molecular Formula: C20H32O5
(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid - Names and Identifiers
| Name | 15-ketoprostaglandin F2A |
| Synonyms | 15-ketoprostaglandin F2A 15-Ketoprostaglandinef2alpha 15-oxo-prostaglandin F2alpha 15-KETO PROSTAGLANDIN F2ALPHA 15-keto Prostaglandin F2 MaxSpecStandard 15-keto Prostaglandin F2α Lipid Maps MS Standard 9,11-Dihydroxy-15-oxo-[5Z,9α,11α,13E]-prosta-5,13-dien-1-oic acid (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid |
| CAS | 35850-13-6 |
| InChI | InChI=1/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,16-19,22-23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t16-,17-,18+,19-/m1/s1 |
(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid - Physico-chemical Properties
| Molecular Formula | C20H32O5 |
| Molar Mass | 352.47 |
| Density | 1.149±0.06 g/cm3(Predicted) |
| Boling Point | 535.2±50.0 °C(Predicted) |
| Flash Point | 291.5°C |
| Vapor Presure | 1.1E-13mmHg at 25°C |
| pKa | 4.76±0.10(Predicted) |
| Storage Condition | −20°C |
| Refractive Index | 1.561 |
(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid - Introduction
15-ketostaglandin F2A (15-ketostaglandin F2A) is a biologically active substance, one of the prostaglandin compounds. It is produced from arachidonic acid after a series of enzymatic reactions.
15-ketoprostaglandin F2A has a variety of physiological functions in vivo, including regulation of blood pressure and blood coagulation, anti-inflammatory and antioxidant effects. Its main role in the organism is to contract the smooth muscle of the uterus, so it is often used in medicine to induce abortion and labor.
The method of preparing 15-ketoprostaglandin F2A is mainly extracted from animal tissues or chemically synthesized. The method of extracting from animal tissues usually includes collecting the prostaglandin in the animal body, and then performing a series of extraction, separation and purification steps to obtain the target product. The method of chemical synthesis uses the technology of organic synthetic chemistry, through the synthesis of precursor compounds and through a series of chemical reactions to obtain the target product.
Regarding safety information, 15-ketoprostaglandin F2A is a biologically active substance that has a certain degree of safety in medical use. However, it may also cause some unpleasant reactions, such as uterine contraction pain, nausea, vomiting, etc. During use, you should follow the doctor's recommendations and pay attention to the appearance of uncomfortable reactions. In addition, for pregnant women and pregnant women, the use of 15-ketoprostaglandin F2A needs to be carried out with caution and under the guidance of a doctor.
15-ketoprostaglandin F2A has a variety of physiological functions in vivo, including regulation of blood pressure and blood coagulation, anti-inflammatory and antioxidant effects. Its main role in the organism is to contract the smooth muscle of the uterus, so it is often used in medicine to induce abortion and labor.
The method of preparing 15-ketoprostaglandin F2A is mainly extracted from animal tissues or chemically synthesized. The method of extracting from animal tissues usually includes collecting the prostaglandin in the animal body, and then performing a series of extraction, separation and purification steps to obtain the target product. The method of chemical synthesis uses the technology of organic synthetic chemistry, through the synthesis of precursor compounds and through a series of chemical reactions to obtain the target product.
Regarding safety information, 15-ketoprostaglandin F2A is a biologically active substance that has a certain degree of safety in medical use. However, it may also cause some unpleasant reactions, such as uterine contraction pain, nausea, vomiting, etc. During use, you should follow the doctor's recommendations and pay attention to the appearance of uncomfortable reactions. In addition, for pregnant women and pregnant women, the use of 15-ketoprostaglandin F2A needs to be carried out with caution and under the guidance of a doctor.
Last Update：2024-04-09 20:49:11
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(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E)-3-oxooct-1-enyl]cyclopentyl]hept-5-enoic acid
Chapelieric acid
Chapelieric acid