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Cat. No.: HY-N1135

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Toxicarol isoflavone

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Toxicarol isoflavone is a natural isoflavone compound found in the leaves of Millettia brandisiana, and it belongs to flavonoid secondary metabolites.

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

Purity: 99.13%
CAS No.: 3044-60-8
Formula: C₂₃H₂₂O₇
Molecular Weight:410.42

Storage:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month

Toxicarol isoflavone Chemical Structure

CAS No.: 3044-60-8

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Use of MCE Products

Fluorescent Dye

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

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

Biological Activity

Description

Toxicarol isoflavone is a natural isoflavone compound found in the leaves of Millettia brandisiana, and it belongs to flavonoid secondary metabolites^[1]^[2].

All Endogenous Metabolite Isoforms :

In Vitro

Toxicarol isoflavone (compound 3) is synthesized via oxidative rearrangement of dihydropyranochalcones with thallium(III) nitrate and structural characterization is performed^[1].
Toxicarol isoflavone (compound 4) shows no DPPH free radical scavenging activity in TLC screening assay^[2].

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

Chemical Information

CAS No. 3044-60-8
Appearance Solid
Molecular Weight 410.42
Formula C₂₃H₂₂O₇
Color Off-white to yellow
SMILES

O=C1C2=C(O)C=C3C(C=CC(C)(C)O3)=C2OC=C1C4=CC(OC)=C(OC)C=C4OC
Structure Classification
- Flavonoids
- Isoflavones
- Phenols
- Monophenols
Initial Source
- Plants
- other families
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	6 months
	-20°C	1 month

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (270 KB)
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Tsukayama M, et al. Synthesis of Pyranoisoflavones by the Oxidative Rearrangement of Dihydropyranochalcones with Thallium(III) Nitrate: Synthesis of Elongatin, Its Angular Isomer, Toxicarol Isoflavone, and Related Compounds. Chemical & Pharmaceutical Bulletin. 1988;36(2):592-600.

[2]. Pancharoen O, et al. Isoflavones and rotenoids from the leaves of Millettia brandisiana. Chem Pharm Bull (Tokyo). 2008;56(6):835-838. [Content Brief]

Calculators

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

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Toxicarol isoflavone

All Endogenous Metabolite Isoforms

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

Toxicarol isoflavone Related Classifications

HY-N1135 Related Classifications