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Picrasidine J
Picrasidine J
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Picrasidine J
Price:
CAS No.: 100234-62-6
Catalog No.: CFN99020
Molecular Formula: C14H14N2O2
Molecular Weight: 242.3 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Yellow powder
Source: The bark of Picrasma quassioides.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Description: Reference standards.
Picrasidine J Description
Source: The bark of Picrasma quassioides.
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
More...

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 4.1271 mL 20.6356 mL 41.2712 mL 82.5423 mL 103.1779 mL
5 mM 0.8254 mL 4.1271 mL 8.2542 mL 16.5085 mL 20.6356 mL
10 mM 0.4127 mL 2.0636 mL 4.1271 mL 8.2542 mL 10.3178 mL
50 mM 0.0825 mL 0.4127 mL 0.8254 mL 1.6508 mL 2.0636 mL
100 mM 0.0413 mL 0.2064 mL 0.4127 mL 0.8254 mL 1.0318 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:
CHEMICAL & PHARMACEUTICAL BULLETIN, 1985, 33(8):3356-3360.
Studies on the alkaloids from Picrasma quassioides Bennet. IV. Structures of picrasidines I, J, and K.[Reference: WebLink]

METHODS AND RESULTS:
Three new β-carboline alkaloids, picrasidine I (I), Picrasidine J (II), and picrasidine K (III), were isolated from the bark of Picrasma quassioides BENNET. The structures were determined on the basis of spectral analyses and chemical transformations.
CFN99020Picrasidine J100234-62-6242.3 C14H14N2O2
CFN97116Dehydrocrenatidine65236-62-6254.3 C15H14N2O2
CFN921221-Acetyl-beta-carboline50892-83-6210.2C13H10N2O
CFN984561-Methoxycarbonyl-beta-carboline3464-66-2226.2 C13H10N2O2
CFN915671-Formyl-beta-carboline20127-63-3196.2C12H8N2O
CFN95291Perlolyrine29700-20-7264.3C16H12N2O2
CFN950231-Methoxycarbonyl-beta-carboline-N-oxide74690-74-7242.2C13H10N2O3
CFN921231-Ethoxycarbonyl-beta-carboline72755-19-2240.3C14H12N2O2
CFN929294-Hydroxy-1-methoxycarbonyl-beta-carboline74690-72-5242.23C13H10N2O3
CFN970374-Methoxy-1-methoxycarbonyl-beta-carboline60807-25-2256.3 C14H12N2O3
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