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Merck

08172

Cycloartenol

≥90% (GC)

Sinonimo/i:

(3S,5R,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-Dimethyl-hex-4-enyl)-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-ol, 9,19-Cyclo-24-lanosten-3β-ol, Handianol

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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C30H50O
Numero CAS:
469-38-5
Peso molecolare:
426.72
UNSPSC Code:
12352211
NACRES:
NA.77
Beilstein/REAXYS Number:
2224850

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form

powder

Quality Level

100

SMILES string

O[C@@H]1C([C@H]2[C@@]3([C@]4([C@H]([C@]5([C@@]([C@H](CC5)[C@@H](CCC=C(C)C)C)(CC4)C)C)CC2)C3)CC1)(C)C

InChI

1S/C30H50O/c1-20(2)9-8-10-21(3)22-13-15-28(7)24-12-11-23-26(4,5)25(31)14-16-29(23)19-30(24,29)18-17-27(22,28)6/h9,21-25,31H,8,10-19H2,1-7H3/t21-,22-,23+,24+,25+,27-,28+,29-,30+/m1/s1

InChI key

ONQRKEUAIJMULO-YBXTVTTCSA-N

assay

≥90% (GC)

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Questo articolo
PHL857291A020201A00110
Cycloartenol ≥90% (GC)

Sigma-Aldrich

08172

Cycloartenol

Cycloartenol phyproof® Reference Substance

PHL85729

Cycloartenol

9-Bromo-16Alpha-Hydroxyprednisolone Pharmaceutical Analytical Impurity (PAI)

USP

1A02020

9-Bromo-16Alpha-Hydroxyprednisolone

6-Beta-Hydroxy Ethinyl Estradiol Pharmaceutical Analytical Impurity (PAI)

USP

1A00110

6-Beta-Hydroxy Ethinyl Estradiol

assay

≥90% (GC)

assay

≥90.0% (HPLC)

assay

-

assay

-

form

powder

form

powder

form

-

form

-

Quality Level

100

Quality Level

-

Quality Level

-

Quality Level

-

Application

  • Genome-Wide Investigation of Oxidosqualene Cyclase Genes Deciphers the Genetic Basis of Triterpene Biosynthesis in Tea Plants - Research on cycloartenol′s synthesis pathways through the genetic study of oxidosqualene cyclase in tea plants, providing insights into the enhancement of plant sterols beneficial for human health (Du et al., 2024).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCM7626
BCCL6369
BCCJ1389
BCCG2376
BCCD5754

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Laurent F Wentzinger et al.
Plant physiology, 130(1), 334-346 (2002-09-13)
To get some insight into the regulatory mechanisms controlling the sterol branch of the mevalonate pathway, tobacco (Nicotiana tabacum cv Bright Yellow-2) cell suspensions were treated with squalestatin-1 and terbinafine, two specific inhibitors of squalene synthase (SQS) and squalene epoxidase
X Qi et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(21), 8233-8238 (2004-05-19)
The evolution of the ability to synthesize specialized metabolites is likely to have been key for survival and diversification of different plant species. Oats (Avena spp.) produce antimicrobial triterpenoids (avenacins) that protect against disease. The oat beta-amyrin synthase gene AsbAS1
Ryousuke Ito et al.
Organic letters, 13(10), 2678-2681 (2011-04-30)
The gene products of AK121211, AK066327, and AK070534 from Oryza sativa encode cycloartenol, parkeol, and achilleol B synthases, respectively. Parkeol synthase is a unique enzyme that affords parkeol as a single product. Achilleol B synthase is the third seco-type triterpene
Wahid Herchi et al.
Plant physiology and biochemistry : PPB, 47(10), 880-885 (2009-07-21)
A comparative study was performed to determine the free sterols content and composition during the development of three varieties of linseed (H52, O116 and P129). Seed samples were collected at regular intervals from 7 to 60 days after flowering (DAF).
Anita Loeschcke et al.
PloS one, 12(12), e0189816-e0189816 (2017-12-28)
Cyclic triterpenes constitute one of the most diverse groups of plant natural products. Besides the intriguing biochemistry of their biosynthetic pathways, plant triterpenes exhibit versatile bioactivities, including antimicrobial effects against plant and human pathogens. While prokaryotes have been extensively used
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