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Cat. No.: HY-N21857

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(4S, 6S)-4-Hydroxypiperitone

(4S, 6S)-4-Hydroxypiperitone is a monoterpene ketone found in the roots of Angelica Pubescens. (4S, 6S)-4-Hydroxypiperitone shows no obvious cytotoxic effect on RAW264.7 cells. (4S, 6S)-4-Hydroxypiperitone can be used in research related to inflammatory immunity and monoterpene biotransformation.

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

CAS No.: 151006-27-8
Formula: C₁₀H₁₆O₂
Molecular Weight:168.23

Storage:

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

(4S, 6S)-4-Hydroxypiperitone Chemical Structure

CAS No.: 151006-27-8

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Use of MCE Products

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

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
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Biological Activity

Description

In Vitro

(4S, 6S)-4-Hydroxypiperitone (compound 8) (50 μM; pretreatment for 2 h; LPS (HY-D1056) 100 ng/mL; 24 h) shows no significant cytotoxicity against RAW 264.7 cells^[1].
(4S, 6S)-4-Hydroxypiperitone (50 μM; 2 h) shows no obvious cytotoxicity in RAW264.7 cells^[1].

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

Cell Viability Assay^[1]

Cell Line:

RAW 264.7
Concentration:

50 μM
Incubation Time:

24 h
Result:

Did not show obvious cytotoxic effects at 50 μM.

Chemical Information

CAS No. 151006-27-8
Molecular Weight 168.23
Formula C₁₀H₁₆O₂
SMILES

CC([C@H]1C(C=C([C@H](C1)O)C)=O)C
Structure Classification
- Terpenoids
- Other Monoterpenes
Initial Source
- Plants
- Umbelliferae
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]. Tian D, et al. Benzannulated 5,5-spiroketal sesquiterpenes from the roots of Angelica Pubescens. Bioorganic chemistry. 2021 Feb;107:104604.

[2]. Grudniewska A, et al. Enantioselectivity of hydroxylation of racemic piperitone by fungi. Chirality. 2010 Nov;22(10):929-35.

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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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