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(+)-(3R,8S)-Falcarindiol

🥰Excellent
Catalog No. T5S1285Cas No. 225110-25-8
Alias Falcarindiol

1. (+)-(3R,8S)-Falcarindiol is a potential new anticancer agent that exerts its activity through inducing ER stress and apoptosis. 2. Falcarindiol induces immunosuppressive effects in vitro and in vivo and might be a novel therapy for autoimmune or allergic diseases. 3. Falcarindiol has protective effect against CCl(4) toxicity , in part, be explained by anti-lipid peroxidation activity associated with the induction of the GSTs including GSTA4.

(+)-(3R,8S)-Falcarindiol
Other Forms of (+)-(3R,8S)-Falcarindiol:
FalcarindiolT7296155297-87-5
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(+)-(3R,8S)-Falcarindiol

🥰Excellent
Catalog No. T5S1285Alias FalcarindiolCas No. 225110-25-8
1. (+)-(3R,8S)-Falcarindiol is a potential new anticancer agent that exerts its activity through inducing ER stress and apoptosis. 2. Falcarindiol induces immunosuppressive effects in vitro and in vivo and might be a novel therapy for autoimmune or allergic diseases. 3. Falcarindiol has protective effect against CCl(4) toxicity , in part, be explained by anti-lipid peroxidation activity associated with the induction of the GSTs including GSTA4.
Pack SizePriceAvailabilityQuantity
1 mg$39In Stock
5 mg$123In Stock
10 mg$197In Stock
25 mg$332In Stock
50 mg$496In Stock
100 mg$693In Stock
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Batch Information

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Purity:>99.99%
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COA HPLC HNMR

Product Introduction

Bioactivity
Description
1. (+)-(3R,8S)-Falcarindiol is a potential new anticancer agent that exerts its activity through inducing ER stress and apoptosis. 2. Falcarindiol induces immunosuppressive effects in vitro and in vivo and might be a novel therapy for autoimmune or allergic diseases. 3. Falcarindiol has protective effect against CCl(4) toxicity , in part, be explained by anti-lipid peroxidation activity associated with the induction of the GSTs including GSTA4.
Targets&IC50
Mycobacterium tuberculosisH37Ra:6 μM (IC50)
SynonymsFalcarindiol
Chemical Properties
Molecular Weight260.37
FormulaC17H24O2
Cas No.225110-25-8
SmilesCCCCCCC\C=C/[C@H](O)C#CC#C[C@H](O)C=C
Relative Density.1.000 g/cm3 (Predicted)
Storage & Solubility Information
Storagekeep away from direct sunlight | Pure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 60 mg/mL (230.44 mM), Sonication is recommended.
Chloroform, Dichloromethane, Ethyl Acetate, Acetone, etc.: Soluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.8407 mL19.2034 mL38.4069 mL192.0344 mL
5 mM0.7681 mL3.8407 mL7.6814 mL38.4069 mL
10 mM0.3841 mL1.9203 mL3.8407 mL19.2034 mL
20 mM0.1920 mL0.9602 mL1.9203 mL9.6017 mL
50 mM0.0768 mL0.3841 mL0.7681 mL3.8407 mL
100 mM0.0384 mL0.1920 mL0.3841 mL1.9203 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Keywords

InhibitorinhibitBacterial3(R),8(S),9(Z)-Falcarindiol(3R,8S)-Falcarindiol(+)(3R,8S)Falcarindiol(+) (3R,8S) Falcarindiol
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