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Cat. No.: HY-N20664

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(+)-Chromazonarol

(Synonyms: (+)-ent-Chromazonarol)

(+)-Chromazonarol ((+)-ent-Chromazonarol) is a marine sesquiterpene hybrid terpene and pimarane-type hybrid terpene Antifungal agent. (+)-Chromazonarol is isolated from the marine sponge Dysidea pallescens. (+)-Chromazonarol inhibits the mycelial growth of Sclerotinia sclerotiorum and Rhizoctonia solani. (+)-Chromazonarol is applicable to research related to Sclerotinia sclerotiorum infection and Rhizoctonia solani infection.

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

CAS No.: 57457-77-9
Formula: C₂₁H₃₀O₂
Molecular Weight:314.46

Storage:

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

(+)-Chromazonarol Chemical Structure

CAS No.: 57457-77-9

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Fluorescent Dye

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

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
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Bioz

Biological Activity

Description

In Vitro

(+)-Chromazonarol (24.1 μM) potently inhibits mycelium growth of Sclerotinia sclerotiorum with an EC₅₀ of 24.1 μM^[2].
(+)-Chromazonarol shows enhanced antifungal activity against mycelium growth of Rhizoctonia solani^[2].

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

Chemical Information

CAS No. 57457-77-9
Molecular Weight 314.46
Formula C₂₁H₃₀O₂
SMILES

C[C@@]12[C@]3([H])[C@](OC4=CC=C(O)C=C4C3)(CC[C@@]1([H])C(C)(CCC2)C)C
Synonyms

(+)-ent-Chromazonarol
Structure Classification
- Terpenoids
- Sesquiterpenes
Initial Source
- Marine natural products
- Sponge
Dysidea pallescens
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]. Wang H S, et al. Divergent Synthesis of Bioactive Marine Meroterpenoids by Palladium‐Catalyzed Tandem Carbene Migratory Insertion[J]. European Journal of Organic Chemistry, 2018, 2018(7): 915-925.

[2]. Zhang S, et al. Expediently Scalable Synthesis and Antifungal Exploration of (+)-Yahazunol and Related Meroterpenoids. Journal of natural products. 2018 Sep 28;81(9):2010-2017. [Content Brief]

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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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