Cajaninstilbene acid

SKU:BHB21901375
Overview
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Cajaninstilbene acid (CAS 87402-84-4) is an inhibitor supplied as a solid. Relevant to Anti-infection research. Molecular formula C21H22O4, molecular weight 338.40 g/mol. Plant-derived (Leguminosae Cajanus cajan (L.) Millsp.).
Purity 95.0%
CAS Number 87402-84-4
Molecular Weight 338.40 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-149049-1MG 1 mg
HY-149049-5MG 5 mg
HY-149049-10MG 10 mg
HY-149049-50MG 50 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1 mg, 5 mg, 10 mg, 50 mg
  • Lead time: varies by selected option.
  • Storage: Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
Alternative names Cajanine
CAS no. 87402-84-4
Applications
  • Functional Assay (In Vitro)
Source Plant — Leguminosae Cajanus cajan (L.) Millsp.
Molecular weight 338.40
Molecular formula C21H22O4
Purity 95.0%
SMILES O=C(O)C1=C(/C=C/C2=CC=CC=C2)C=C(OC)C(C/C=C(C)\C)=C1O
Form Solid
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-149049
Main SKU BHB21901375
Inhibitors

Compound Overview

Cajaninstilbene acid, also known as Cajanine, is a potent inhibitor of HCV, with an IC50 value of 3.17 μM. It inhibits HCV replication by down-regulating the cellular protein chondroitin sulfate N-acetylgalactosaminyltransferase 1[1]. It is supplied as a solid (C21H22O4, MW 338.40) at 95.0% purity.

Physical & Chemical Properties

CAS Number 87402-84-4
Molecular Formula C21H22O4
Molecular Weight 338.40 g/mol
Purity 95.0%
Appearance Solid
Structure Classification Phenylpropanoids Simple Phenylpropanols
SMILES O=C(O)C1=C(/C=C/C2=CC=CC=C2)C=C(OC)C(C/C=C(C)\C)=C1O
Signaling Pathway Anti-infection
Initial Source Plant — Leguminosae Cajanus cajan (L.) Millsp.
Solubility In Vitro: DMSO: ≥ 50 mg/mL (147.75 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) * "≥" means soluble, but saturation unknown.
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description. Peer-reviewed publications that used this product are listed under References.

[1]. Ji XY, et al. Design and Synthesis of Cajanine Analogues against Hepatitis C Virus through Down-Regulating Host Chondroitin Sulfate N-Acetylgalactosaminyltransferase 1. J Med Chem. 2016 Nov 23;59(22):10268-10284.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO≥ 50 mg/mL (147.75 mM)use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.

In Vivo

Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.

Protocol 1

Composition10% DMSO + 40% PEG300 + 5% Tween-80 + 45% saline
Result≥ 1.25 mg/mL (3.69 mM); clear solution
How to prepareGives a clear solution at ≥ 1.25 mg/mL (saturation not determined). For 1 mL of working solution: add 100 μL DMSO stock (12.5 mg/mL) to 400 μL PEG300; then 50 μL Tween-80; then 450 μL saline to bring the volume to 1 mL. Saline: dissolve 0.9 g sodium chloride in ddH2O and make up to 100 mL.

Protocol 2

Composition10% DMSO + 90% Corn Oil
Result1.25 mg/mL (3.69 mM); suspension; requires sonication
How to prepareGives a suspension at 1.25 mg/mL. The suspension is suitable for oral and intraperitoneal dosing. For 1 mL of working solution: add 100 μL DMSO stock (12.5 mg/mL) to 900 μL corn oil.

Data provided by the manufacturer.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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