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Cat. No.: HY-W728218

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3-Dehydro-teasterone

3-Dehydro-teasterone is a brassinosteroid biosynthesis intermediate and a substrate of 3-dehydroteasterone reductase (3-dehydroteasterone reductase). 3-Dehydro-teasterone can be used in studies related to plant brassinosteroid biosynthesis and other related research.

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CAS No.: 124853-28-7
Formule: C₂₈H₄₆O₄
Masse moléculaire:446.66

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

3-Dehydro-teasterone Chemical Structure

CAS No.: 124853-28-7

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Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
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Activité biologique

Description

In Vitro

3-Dehydro-teasterone (2 μg/500 μL enzyme solution; 37°C; 30 min) is converted to typhasterol by 3-dehydroteasterone reductase in the crude cytosolic fraction prepared from Marchantia polymorpha cultured cells, with a substrate conversion rate of 2.1%; no corresponding reductase activity is detected in the microsomal fraction^[2].
3-Dehydro-teasterone (10-1000 ng/plant; 1 μL ethanol solution; injected at the leaf tip; single dose; 3 days) effectively increases lamina joint bending in d2-2 mutant rice seedlings and similarly increases lamina joint bending in wild-type rice seedlings^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .

Chemical Information

CAS No. 124853-28-7
Masse moléculaire 446.66
Formule C₂₈H₄₆O₄
SMILES

C[C@@]12[C@](CC[C@]2([H])[C@H](C)[C@@H](O)[C@H](O)[C@@H](C)C(C)C)([H])[C@@]3([H])[C@@](CC1)([H])[C@@]4([C@@](CC(CC4)=O)([H])C(C3)=O)C
Structure Classification
- Terpenoids
- Triterpenes
- Steroids
Initial Source
- Microorganisms
Cystoseira myrica
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Instruction de manipulation (2659 KB)

Références

[1]. Hong Z, et al. A rice brassinosteroid-deficient mutant, ebisu dwarf (d2), is caused by a loss of function of a new member of cytochrome P450. The Plant cell. 2003 Dec;15(12):2900-10.

[2]. Park SH, et al. In Vivo and in Vitro Conversion of Teasterone to Typhasterol in Cultured Cells of Marchantia polymorpha. Plant Cell Physiol. 1999;40(9):955-960.

[3]. Suzuki H, et al. Possible Involvement of 3-Dehydroteasterone in the Conversion of Teasterone to Typhasterol in Cultured Cells of Catharanthus roseus. Biosci Biotechnol Biochem. 1994;58(6):1186-1188.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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