Introduction:Basic information about CAS 23434-88-0|Tetrahydropiperin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Tetrahydropiperin |
|---|
| CAS Number | 23434-88-0 | Molecular Weight | 289.369 |
|---|
| Density | 1.2±0.1 g/cm3 | Boiling Point | 469.9±24.0 °C at 760 mmHg |
|---|
| Molecular Formula | C17H23NO3 | Melting Point | 41ºC |
|---|
| MSDS | / | Flash Point | 238.0±22.9 °C |
|---|
Names
| Name | 5-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylpentan-1-one |
|---|
| Synonym | More Synonyms |
|---|
Tetrahydropiperin BiologicalActivity
| Description | Tetrahydropiperine, a cyclohexyl analogue of piperine, is the first natural aryl pentanamide from Piper longum[1]. Tetrahydropiperine (compound 14) inhibits the cytochrome P450 (CYP) isoform CYP1A1/arylhydrocarbon hydroxylase (AHH; IC50=23 µM)[2]. |
|---|
| Related Catalog | Research Areas >>CancerSignaling Pathways >>Metabolic Enzyme/Protease >>Cytochrome P450 |
|---|
| Target | CYP1A1:23 μM (IC50) |
|---|
| References | [1]. Madhusudhan P, et al. Tetrahydropiperine, the first natural aryl pentanamide from Piper longum. Biochem Syst Ecol. 2001 May;29(5):537-538. [2]. Koul S, et al. Structure-activity relationship of piperine and its synthetic analogues for their inhibitory potentials of rat hepatic microsomal constitutive and inducible cytochromeP450 activities. Bioorg Med Chem. 2000 Jan;8(1):251-68. |
|---|
Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
|---|
| Boiling Point | 469.9±24.0 °C at 760 mmHg |
|---|
| Melting Point | 41ºC |
|---|
| Molecular Formula | C17H23NO3 |
|---|
| Molecular Weight | 289.369 |
|---|
| Flash Point | 238.0±22.9 °C |
|---|
| Exact Mass | 289.167786 |
|---|
| PSA | 38.77000 |
|---|
| LogP | 3.67 |
|---|
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
|---|
| Index of Refraction | 1.556 |
|---|
| InChIKey | APZYKUZPJCQGPP-UHFFFAOYSA-N |
|---|
| SMILES | O=C(CCCCc1ccc2c(c1)OCO2)N1CCCCC1 |
|---|
| Storage condition | -20℃ |
|---|
Synonyms
| 1-[5-(1,3-Benzodioxol-5-yl)pentanoyl]piperidine |
| Tetrahydropiperidine |
| 5-(1,3-Benzodioxol-5-yl)-1-(piperidin-1-yl)pentan-1-one |
| Tetrahydropiperin |
| 1-Pentanone, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)- |
| 5-(1,3-Benzodioxol-5-yl)-1-(1-piperidinyl)-1-pentanone |
| Piperidine, 1-[5-(1,3-benzodioxol-5-yl)-1-oxopentyl]- |
| Cosmoperine |
| Tetrahydropiperine |