JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB142425

20-Hydroxyecdysone (Ecdysterone), Steroid invertebrate hormone

Be the first to review this product! Submit a review

|

(4 Publications)

MW 480.6 Da, Purity >98%. Steroid invertebrate hormone. Regulates molting, metamorphosis and reproduction in arthropods. Neuroprotective against oxidative stress in mammals. Inhibits NF-κB activation and iNOS expression. Antioxidant and apoptotic agent.

View Alternative Names

AA407097, AI194287, AU018802, DKFZp686H13163, EC 2.5.1.18, GSTO 1-1, GSTO1_HUMAN, GSTTLp28, GSTX, Glutathione S-transferase omega, Glutathione S-transferase omega 1-1, Glutathione S-transferase omega-1, Glutathione transferase omega 1, Glutathione-S-transferase like, Glutathione-dependent dehydroascorbate reductase, Gtsttl, MGC94845, MMA(V) reductase, Monomethylarsonic acid reductase, OTTHUMP00000020429, S-(Phenacyl)glutathione reductase, SPG-R

1 Images
Chemical Structure - 20-Hydroxyecdysone (Ecdysterone), Steroid invertebrate hormone (AB142425)
  • Chemical Structure

Lab

Chemical Structure - 20-Hydroxyecdysone (Ecdysterone), Steroid invertebrate hormone (AB142425)

2D chemical structure image of ab142425, 20-Hydroxyecdysone (Ecdysterone), Steroid invertebrate hormone

Key facts

CAS number

5289-74-7

Purity

>98%

Form

Solid

form

Molecular weight

480.6 Da

Molecular formula

C<sub>2</sub><sub>7</sub>H<sub>4</sub><sub>4</sub>O<sub>7</sub>

PubChem

5459840

Nature

Synthetic

Solubility

Soluble in water to 10 mM

Soluble in ethanol to 100 mM

Soluble in DMSO to 100 mM

Biochemical name

20-Hydroxyecdysone

Biological description

Steroid invertebrate hormone. Regulates molting, metamorphosis and reproduction in arthropods. Neuroprotective against oxidative stress in mammals. Inhibits NF-κB activation and iNOS expression. Antioxidant and apoptotic agent.

Canonical smiles

CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O

Isomeric smiles

C[C@]12CC[C@H]3C(=CC(=O)[C@H]4[C@@]3(C[C@@H]([C@@H](C4)O)O)C)[C@@]1(CC[C@@H]2[C@](C)([C@@H](CCC(C)(C)O)O)O)O

InChi

InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15-,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1

InChiKey

NKDFYOWSKOHCCO-YPVLXUMRSA-N

IUPAC Name

(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Glutathione S-transferase Omega 1 also known as GSTO1 or p28 is an enzyme that plays an important role in detoxification processes. It belongs to the omega class of glutathione S-transferases and has a molecular mass of approximately 28 kDa. This enzyme is expressed in various human tissues including the liver kidney and brain where it performs important metabolic functions. GSTO1 is not only involved in catalyzing the reduction of hydroxyecdysone metabolites such as ecdysterone (20-hydroxyecdysone) but also participates in modulating cellular responses to oxidative stress.
Biological function summary

GSTO1 is part of a complex network of proteins involved in protecting cells from oxidative damage. This enzyme takes part in antioxidant defense by catalyzing the conjugation of glutathione with harmful compounds facilitating their elimination. As a part of detoxification processes GSTO1 assists in maintaining cellular redox balance. Such activities are essential for several physiological functions including the metabolism of steroid compounds which can relate to ecdysteroid steroid activity. Its activity influences not only metabolic stability but also cell survival and integrity.

Pathways

GSTO1 functions in significant signaling pathways particularly in glutathione metabolism and stress response pathways. It interacts with proteins such as glutaredoxins and thioredoxins playing a role in regulating redox-sensitive signaling. Through its involvement in glutathione pathways GSTO1 helps mitigate damage from reactive oxygen species (ROS) and supports cellular repair mechanisms. Its actions link it with the broader antioxidant networks that maintain cellular homeostasis and modulate stress-induced pathways.

GSTO1 has connections to neurological and inflammatory conditions. For instance alterations in GSTO1 expression have been associated with Alzheimer's disease where oxidative stress plays a pivotal role. Similarly it seems implicated in inflammatory disorders due to its capacity to modulate inflammatory responses. Dysfunctional GSTO1 activity can result in an imbalance in oxidative stress pathways linking it with disease-related proteins like amyloid beta in neurodegenerative diseases and inflammatory cytokines in immune-related disorders.

Product protocols

Publications (4)

Recent publications for all applications. Explore the full list and refine your search

Communications biology 8:983 PubMed40603560

2025

Lysyl-tRNA synthetase orchestrates translation and hormone signaling during reproduction in Aedes aegypti mosquitoes.

Applications

Unspecified application

Species

Unspecified reactive species

Shan Li,Xueli Wang,Haoran Lu,Alexander S Raikhel,Zhen Zou

Scientific reports 11:18807 PubMed34552169

2021

Activation of EGFR signaling by Tc-Vein and Tc-Spitz regulates the metamorphic transition in the red flour beetle Tribolium castaneum.

Applications

Unspecified application

Species

Unspecified reactive species

Sílvia Chafino,David Martín,Xavier Franch-Marro

The Journal of cell biology 219: PubMed31940424

2020

Trpml controls actomyosin contractility and couples migration to phagocytosis in fly macrophages.

Applications

Unspecified application

Species

Unspecified reactive species

Sandra Sofía Edwards-Jorquera,Floris Bosveld,Yohanns A Bellaïche,Ana-María Lennon-Duménil,Álvaro Glavic

Mechanisms of development 154:277-286 PubMed30096416

2018

An in vitro method for studying subcellular rearrangements during cell polarization in Drosophila melanogaster hemocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Sandra Sofía Edwards,María Graciela Delgado,Guilherme Pedreira de Freitas Nader,Matthieu Piel,Yohanns Bellaïche,Ana María Lennon-Duménil,Álvaro Glavic
View all publications

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com