Shipping to United States We Offer Worldwide Shipping
Login Wishlist

(+)-Odorinol

$1,120 $1,008

  • Brand : BIOFRON

  • Catalogue Number : BN-O0277

  • Specification : 97%(HPLC)

  • CAS number : 72755-22-7

  • Formula : C18H24N2O3

  • Molecular Weight : 316.4

  • PUBCHEM ID : 6440456

  • Volume : 5MG

In stock

Quantity
Checkout Bulk Order?

Catalogue Number

BN-O0277

Analysis Method

HPLC,NMR,MS

Specification

97%(HPLC)

Storage

-20℃

Molecular Weight

316.4

Appearance

Powder

Botanical Source

This product is isolated and purified from the herbs of Aglaia odorata

Structure Type

Alkaloids

Category

Standards;Natural Pytochemical;API

SMILES

CCC(C)(C(=O)NC1CCCN1C(=O)C=CC2=CC=CC=C2)O

Synonyms

Butanamide, 2-hydroxy-2-methyl-N-[(2R)-1-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-2-pyrrolidinyl]-, (2S)- /(2S)-2-Hydroxy-2-methyl-N-{(2R)-1-[(2E)-3-phenyl-2-propenoyl]-2-pyrrolidinyl}butanamide

IUPAC Name

(2S)-2-hydroxy-2-methyl-N-[(2R)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]butanamide

Applications

Density

1.2±0.1 g/cm3

Solubility

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

Flash Point

309.8±30.1 °C

Boiling Point

588.6±50.0 °C at 760 mmHg

Melting Point

InChl

InChI=1S/C18H24N2O3/c1-3-18(2,23)17(22)19-15-10-7-13-20(15)16(21)12-11-14-8-5-4-6-9-14/h4-6,8-9,11-12,15,23H,3,7,10,13H2,1-2H3,(H,19,22)/b12-11+/t15-,18+/m1/s1

InChl Key

ZSSIVXBCHJDPDR-IHUUNXMQSA-N

WGK Germany

RID/ADR

HS Code Reference

2933990000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:72755-22-7) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

11725964

Abstract

In the course of our continuing search for novel cancer chemo-preventive agents from natural sources, we have carried out a primary screening in vitro assay of the compounds isolated from Aglaia odorata. Consequently, aminopyrrolidine-diamides, odorine and odorinol, were obtained as active constituents. These compounds exhibited potent anti-carcinogenic effects in a two-stage carcinogenesis test of mouse skin induced by 7,12-dimethylbenz[a]anthracene (DMBA) as an initiator and 12-O-tetradecanoylphorbol-13-acetate (TPA) as a promoter. Further, both compounds showed remarkable inhibitory effects in two-stage mouse skin carcinogenesis models induced by nitric oxide (NO) donors such as (+/-)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexenamide (NOR-1) or peroxynitrite as an initiator and TPA as a promoter. From these results, it was concluded that odorine and odorinol inhibited both the initiation and promotion stages of two-stage skin carcinogenesis.

Title

Cancer chemopreventive activity of odorine and odorinol from Aglaia odorata.

Author

Inad A1, Nishino H, Kuchide M, Takayasu J, Mukainaka T, Nobukuni Y, Okuda M, Tokuda H.

Publish date

2001 Nov;

PMID

3628559

Title

Antiviral activity of (+)-odorinol.

Author

Joshi MN, Chowdhury BL, Vishnoi SP, Kapil RS.

Publish date

1987 Jun