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16-Nor-15-oxodehydroabietic acid
16-Nor-15-oxodehydroabietic acid
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 16-Nor-15-oxodehydroabietic acid
Price:
CAS No.: 200813-31-6
Catalog No.: CFN96033
Molecular Formula: C19H24O3
Molecular Weight: 300.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Pinus massoniana
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Biological Activity
Description: 16-Nor-15-oxodehydroabietic acid is a natural product from Pinus massoniana.
16-Nor-15-oxodehydroabietic acid Description
Source: The herbs of Pinus massoniana
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.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.3289 mL 16.6445 mL 33.2889 mL 66.5779 mL 83.2224 mL
5 mM 0.6658 mL 3.3289 mL 6.6578 mL 13.3156 mL 16.6445 mL
10 mM 0.3329 mL 1.6644 mL 3.3289 mL 6.6578 mL 8.3222 mL
50 mM 0.0666 mL 0.3329 mL 0.6658 mL 1.3316 mL 1.6644 mL
100 mM 0.0333 mL 0.1664 mL 0.3329 mL 0.6658 mL 0.8322 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.
Protocol
Structure Identification:
Phytochemistry, 1997 , 46 (6) :1051-1057.
Abietane diterpene acids and other constituents from the leaves of Larix kaempferi[Reference: WebLink]

METHODS AND RESULTS:
The new diterpene acids were isolated from the leaves of Larix kaempferi, together with two known sesquiterpenes, (−)-α-cadinol and oplopanone, and 10 known diterpenes, larixol, dehydroabietinol, 7-oxo-dehydroabietinol, 7-oxodehydroabietic acid, 9α,13α-epidioxyabiet-8(14)-en-18-oic acid, 9β,13β-epidioxyabiet-8(14)-en-18-oic acid, dehydroabietic acid, 7α-hydroxydehydroabietic acid, 8α,9α,13α,14α-diepoxyabietan-18-oic acid and 15-hydroxydehydroabetic acid.
CONCLUSIONS:
The new acids and their methyl esters were characterized as methyl abieta-8,11,13,15-tetraen-18-oic acid, methyl 16-Nor-15-oxodehydroabietic acid and methyl 12,15-dihydroxydehydroabietic acid, on the basis of chemical and spectroscopic evidence.
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