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Referencia número: HY-W168309A

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trans-Caffeic aldehyde

Name: trans-Caffeic aldehyde
Brand: MedChemExpress
SKU: HY-W168309A
Price: 405.00 USD
Availability: InStock
Rating: 5 (1 reviews)

Trans-Caffeic aldehyde is a type of phenylpropanoid compound, which was discovered in the secondary metabolites of the actinomycete Acrocarpospora punica. Trans-Caffeic aldehyde does not exhibit inhibitory activity against NO production in the mouse macrophage (RAW 264.7) model induced by LPS (HY-D1056).

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No. CAS: 141632-15-7
Fòrmula: C₉H₈O₃
Peso molecular:164.16

Almacenamiento:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (265 KB)

trans-Caffeic aldehyde Chemical Structure

No. CAS: 141632-15-7

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Descripciòn

Ver todos los productos específicos de isoformas Endogenous Metabolite :

Cellular Effect

Cell Line	Type	Value	Description	References
A-431	IC₅₀	>30 μg/mL Compound: 1	Inhibitory concentration required against A 431 human epidermoid carcinoma cell line Inhibitory concentration required against A 431 human epidermoid carcinoma cell line	[PMID: 11354370]
B16	IC₅₀	>30 μg/mL Compound: 1	Inhibitory concentration against B16 murine melanoma cell line Inhibitory concentration against B16 murine melanoma cell line	[PMID: 11354370]
HCT-116	IC₅₀	>30 μg/mL Compound: 1	Inhibitory concentration against HCT 116 human colon cancer cell line Inhibitory concentration against HCT 116 human colon cancer cell line	[PMID: 11354370]
HeLa	EC₅₀	2.58 μM Compound: 17	Induction of cell surface translocation of MR1 in human HeLa overexpressing MR1 assessed as increase in MR1 cell surface levels incubated for 8 hrs followed by labeling with PE-conjugated anti-hMR1 antibody by flow cytometry analysis Induction of cell surface translocation of MR1 in human HeLa overexpressing MR1 assessed as increase in MR1 cell surface levels incubated for 8 hrs followed by labeling with PE-conjugated anti-hMR1 antibody by flow cytometry analysis	[PMID: 37638616]

Chemical Information

No. CAS 141632-15-7
Peso molecular 164.16
Fòrmula C₉H₈O₃
SMILES

O=C/C=C/C1=CC(O)=C(C=C1)O
Structure Classification
- Phenols
- Polyphenols
Initial Source
- Microorganism
Acrocarpospora punica
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureza y Documentación

Select Batch:

Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

Ficha de datos (265 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instrucciones de manejo (2659 KB)

Referencias

[1]. Cheng MJ, et al. Antifungal Activities of Compounds Produced by Newly Isolated Acrocarpospora Strains. Antibiotics (Basel). 2023 Jan 5;12(1):95. [Content Brief]

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How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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trans-Caffeic aldehyde

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trans-Caffeic aldehyde

Ver todos los productos específicos de isoformas Endogenous Metabolite

Actividad biológica

Descripciòn

Cellular Effect

Chemical Information

Pureza y Documentación

Referencias

Calculators

Help & FAQs

trans-Caffeic aldehyde Related Classifications

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