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Postion:Product Catalog >Natural Products>Alkaloids>Cyclo(L-Phe-trans-4-hydroxy-L-Pro)
Cyclo(L-Phe-trans-4-hydroxy-L-Pro)
  • Cyclo(L-Phe-trans-4-hydroxy-L-Pro)

Cyclo(L-Phe-trans-4-hydroxy-L-Pro) NEW

Price $68 $159 $258
Package 1mg 5mg 10mg
Supply Ability: 10g
Update Time: 2026-06-10

Product Details

Product Name: Cyclo(L-Phe-trans-4-hydroxy-L-Pro) CAS No.: 118477-06-8
Purity: 99.87% Supply Ability: 10g
Release date: 2026/06/10

Product Introduction

Bioactivity

NameCyclo(L-Phe-trans-4-hydroxy-L-Pro)
DescriptionCyclo(L-Phe-trans-4-hydroxy-L-Pro) (Cyclo(L-phenylalanyl-trans-4-hydroxy-L-proline)) is a natural product found in Phellinus igniarius.
In vitroWe previously identified Streptomyces griseus as an anti-cancer agent (Kim et al., 2014). In this study, we isolated compounds from S. griseus and evaluated their anticancer effect and toxicity in vitro and in vivo. METHODS AND RESULTS: Preparative centrifugal partition chromatography (CPC) was used to obtain three compounds, cyclo(L-[4-hydroxyprolinyl]- L -leucine], Cyclo(L-Phe-trans-4-hydroxy-L-Pro) and phenethyl acetate (PA). We chose PA, which had the highest anticancer activity, as a target compound for further experiments. PA induced the formation of apoptotic bodies, DNA fragmentation, DNA accumulation in G0/G1 phase, and reactive oxygen species (ROS) formation. Furthermore, PA treatment increased Bax/Bcl-xL expression, activated caspase-3, and cleaved poly-ADP-ribose polymerase (PARP) in HL-60 cells. Simultaneous evaluation in vitro and in vivo, revealed that PA exhibited no toxicity in Vero cells and zebrafish embryos. CONCLUSIONS: We revealed, for the first time, that PA generates ROS, and that this ROS accumulation induced the Bcl signaling pathway[1].
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility InformationDMSO : 50 mg/mL (192.09 mM), Sonication is recommended.
KeywordsCyclo(L-Phe-trans-4-hydroxy-L-Pro)
Inhibitors RelatedCalcium Propionate | Dehydroacetic acid sodium | Potassium gluconate | D-Gluconic acid (solution) (50% in H2O) | Sulfacetamide sodium | Terbinafine hydrochloride | Benzyl propionate | Sodium formate | Magnesium acetate tetrahydrate | Geraniol | L-Citronellol | Benzimidazole
Related Compound LibrariesMarine Natural Product Library | Anti-Tumor Natural Product Library | Bioactive Compound Library | Cyclic Peptide Library | Natural Product Library | Microbial Natural Product Library | Natural Product Library for HTS | RO5 Drug-like Natural Product Library | Bioactive Compounds Library Max

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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6YR United StatesUnited States
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, MA
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