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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.

For research use only. We do not sell to patients.

CAS No.: 124853-28-7
Formula: C₂₈H₄₆O₄
Molecular Weight:446.66

Storage:

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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Use of MCE Products

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

Biological Activity
- Description
- In Vitro
Chemical Information
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Biological Activity

Description

In Vitro

Lipid MetabolismOthers

Lipid Metabolism

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].

Others

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
Molecular Weight 446.66
Formula 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
- Microorganism
Cystoseira myrica
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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

Purity & Documentation

Handling Instructions (2659 KB)

References

[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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