N-(P-Amylcinnamoyl)Anthranilic Acid
N-(P-Amylcinnamoyl)Anthranilic Acid structure
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Common Name | N-(P-Amylcinnamoyl)Anthranilic Acid | ||
|---|---|---|---|---|
| CAS Number | 99196-74-4 | Molecular Weight | 337.41200 | |
| Density | 1.178±0.06 g/cm3 (20 °C, 760 mmHg) | Boiling Point | 563.1±50.0 °C (760 mmHg) | |
| Molecular Formula | C21H23NO3 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS09 |
Signal Word | Warning | |
| Name | Benzoic acid, 2-[[(2E)-1-oxo-3-(4-pentylphenyl)-2-propen-1-yl]amino] |
|---|---|
| Synonym | More Synonyms |
| Density | 1.178±0.06 g/cm3 (20 °C, 760 mmHg) |
|---|---|
| Boiling Point | 563.1±50.0 °C (760 mmHg) |
| Molecular Formula | C21H23NO3 |
| Molecular Weight | 337.41200 |
| Exact Mass | 337.16800 |
| PSA | 66.40000 |
| LogP | 4.84240 |
| InChIKey | GAMRBCZMOOMBSQ-CCEZHUSRSA-N |
| SMILES | CCCCCc1ccc(C=CC(=O)Nc2ccccc2C(=O)O)cc1 |
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Des-Arg9-bradykinin causes kinin B1 receptor mediated endothelium-independent contractions in endotoxin-treated porcine coronary arteries.
Pharmacol. Res. 90 , 18-24, (2014) This study examined responses of isolated pig coronary arteries after kinin B1 receptor induction by endotoxin. Des-Arg9-bradykinin (DBK) induced concentration-dependent, endothelium-independent contr... |
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Enhanced cytotoxicity in triple-negative and estrogen receptor‑positive breast adenocarcinoma cells due to inhibition of the transient receptor potential melastatin-2 channel.
Oncol. Rep. 34 , 1589-98, (2015) We previously demonstrated a unique protective role for the transient receptor potential, melastatin-2 (TRPM2) cation channel in breast cancer cells. In the present study, we investigated the chemothe... |
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Diglycolic acid is the nephrotoxic metabolite in diethylene glycol poisoning inducing necrosis in human proximal tubule cells in vitro.
Toxicol. Sci. 124 , 35-44, (2011) Diethylene glycol (DEG), a solvent and chemical intermediate, can produce an acute toxic syndrome, the hallmark of which is acute renal failure due to cortical tubular degeneration and proximal tubula... |
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Name: Inhibition of human TRPM2 expressed in HEK293 cells assessed as reduction in ADPR-ind...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily M member 2
External Id: CHEMBL4154411
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Name: Inhibition of PLA2 (unknown origin) using soybean phosphatidylcholine as substrate at...
Source: ChEMBL
Target: Phospholipase A2
External Id: CHEMBL4835360
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Name: Human TRPC3 (Transient Receptor Potential channels)
Source: IUPHAR-DB
Target: TRPC3 (Transient Receptor Potential channels) [Homo sapiens]
External Id: 488_Human
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Name: Inhibition of human TRPM2 expressed in HEK293 cells assessed as reduction in ADPR-ind...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily M member 2
External Id: CHEMBL4154412
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Name: Agonist activity at human TRPA1 Phe909Ala mutant expressed in HEK293 cells assessed a...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily A member 1
External Id: CHEMBL4347317
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Name: Inhibition of human TRPM8 expressed in HEK293T cells assessed as blocked of menthol-a...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily M member 8
External Id: CHEMBL4835357
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Name: Agonist activity at human TRPA1 Phe909Ala mutant expressed in HEK293 cells assessed a...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily A member 1
External Id: CHEMBL4347316
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|
Name: Inhibition of PLA2 (unknown origin) using soybean phosphatidylcholine as substrate at...
Source: ChEMBL
Target: Phospholipase A2
External Id: CHEMBL4835362
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Name: Inhibition of human TRPM2 expressed in HEK293T cells cotransfected with GFP assessed ...
Source: ChEMBL
Target: Transient receptor potential cation channel subfamily M member 2
External Id: CHEMBL4844234
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Name: Human TRPC6 (Transient Receptor Potential channels)
Source: IUPHAR-DB
Target: TRPC6 (Transient Receptor Potential channels) [Homo sapiens]
External Id: 491_Human
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| BML 264 |
| N-(P-AMYLCINNAMOYL)ANTHRANILIC ACID |