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16beta,17-Dihydroxy-ent-kaurane-19-oic acid
16beta,17-Dihydroxy-ent-kaurane-19-oic acid
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 16beta,17-Dihydroxy-ent-kaurane-19-oic acid
Price:
CAS No.: 74365-74-5
Catalog No.: CFN93316
Molecular Formula: C20H32O4
Molecular Weight: 336.47 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Siegesbeckia orientalis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: 16beta,17-Dihydroxy-ent-kaurane-19-oic acid as an anti-HIV principle, it showed significant activity against HIV replication in H9 lymphocyte cells with an EC50 value of 0.8 microgram/mL. It also possesses the activities of decompression and blood viscosity depression.
Targets: HIV
In vitro:
J Nat Prod. 1996 Jun;59(6):635-7.
Identification of ent-16 beta, 17-dihydroxykauran-19-oic acid as an anti-HIV principle and isolation of the new diterpenoids annosquamosins A and B from Annona squamosa.[Pubmed: 8786370 ]

METHODS AND RESULTS:
Phytochemical analysis of the fruits of Annona squamosa yielded 12 known kaurane derivatives (1-11, 13) and two new kaurane diterpenoids, which have been named annosquamosin A (16 beta-hydroxy-17-acetoxy-ent-kauran-19-al) (12) and annosquamosin B (19-nor-ent-kaurane-4 alpha,16 beta,-17-triol) (14). The structures of the new compounds were established by spectral analyses and chemical evidence.
CONCLUSIONS:
Among these 14 compounds, 16 beta, 17-dihydroxy-ent-kauran-19-oic acid (16beta,17-Dihydroxy-ent-kaurane-19-oic acid, 2) showed significant activity against HIV replication in H9 lymphocyte cells with an EC50 value of 0.8 microgram/mL (therapeutic index > 5).
Yao Xue Xue Bao. 2007 Feb;42(2):166-70.
Diterpenes from Helianthus annuus and their cytotoxicity in vitro.[Pubmed: 17518044]

METHODS AND RESULTS:
To search for bioactive compounds from the flower disc of Helianthus annuus L., chromatography was used to isolate and purify the chemical constituents, their structures were identified by spectral analysis, MTT method was applied to investigate their cytotoxic activities, some compounds showed moderate cytotoxic activities on SF-268, MCF-7 and HepG2 cell lines. Eleven compounds were obtained from the flower disc of H. annuus, and identified as ent-kaurane-2alpha, 16alpha-diol (1) and entkaurane-15alpha,16alpha-epoxy-17-al-19-oic acid (2), and nine known diterpenes, ent-kaurane-16P-ol (3), phyllocladan-16beta-ol (4) , ent-atisan-16a-ol (5) , grandifloric acid (6) , angeloylgrandifloric acid (7), ent-kaurane-16-en-19-oic acid (8), ent-kaurane-17-hydroxy-15-en-19-oic acid (9), ent-kaurane-16beta, 17-dihydroxy-19-oic acid (16beta,17-Dihydroxy-ent-kaurane-19-oic acid,10), and ciliaric acid (11).
CONCLUSIONS:
Compounds 1 and 2 are new compounds, some compounds showed cytotoxic activities on SF-268, MCF-7 and HepG2 cell lines.
In vivo:
Baiqiuen Yike Daxue Xuebao,Jan 2001, 27(5):472-474.
Effects of ent-16#beta#, 17-dihydroxy-kauran-19-oic acid on decompression and blood viscosity[Reference: WebLink]

METHODS AND RESULTS:
ABP, LVSP, ±dp/dt_(max), HR, DBP and blood viscosity of rabbits were depressed after duodenum administration compared with before drug. ent-16#beta#, 17-dihydroxy-kauran-19-oic acid(16beta,17-Dihydroxy-ent-kaurane-19-oic acid)possesses the activities of decompression and blood viscosity depression.
16beta,17-Dihydroxy-ent-kaurane-19-oic acid Description
Source: The herbs of Siegesbeckia orientalis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.972 mL 14.8602 mL 29.7203 mL 59.4407 mL 74.3008 mL
5 mM 0.5944 mL 2.972 mL 5.9441 mL 11.8881 mL 14.8602 mL
10 mM 0.2972 mL 1.486 mL 2.972 mL 5.9441 mL 7.4301 mL
50 mM 0.0594 mL 0.2972 mL 0.5944 mL 1.1888 mL 1.486 mL
100 mM 0.0297 mL 0.1486 mL 0.2972 mL 0.5944 mL 0.743 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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