| Size | Price | Stock | Qty |
|---|---|---|---|
| 1mg |
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| 5mg |
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| Other Sizes |
| Targets |
Nucleic acids (specifically binds to guanine-rich regions without intercalation, acting as a conformational probe) [2]
Lysosomes (stabilizes lysosomal membranes and exhibits anti-proteolytic activity) [1] |
|---|---|
| ln Vitro |
Hydroxystilbamidine demonstrated significant immunosuppressive effects by inhibiting the release of lysosomal enzymes from macrophages. Treatment with 10 μg/mL reduced β-glucuronidase release by 50% in cultured mouse peritoneal macrophages, indicating lysosomal stabilization and suppression of inflammatory responses. [1]
The drug exhibited antifungal activity against Blastomyces dermatitidis at concentrations of 1–5 μg/mL, disrupting fungal cell integrity through lysosome-mediated mechanisms. [1] In nucleic acid binding studies, Hydroxystilbamidine selectively bound to double-stranded RNA and guanine-rich DNA regions via minor groove interactions, altering nucleic acid conformation without intercalation. This was confirmed by spectral shifts (absorption peak at 335 nm) and fluorescence quenching assays. [2] |
| ln Vivo |
Intraperitoneal administration of 10 mg/kg Hydroxystilbamidine in mice suppressed delayed-type hypersensitivity (DTH) responses to sheep red blood cells by 70%, attributed to lysosome stabilization and reduced protease release from immune cells. [1]
|
| Enzyme Assay |
Lysosomal enzyme release was quantified by measuring β-glucuronidase activity in supernatants of mouse peritoneal macrophages. Cells were treated with Hydroxystilbamidine (0.1–10 μg/mL) for 1 hour, followed by zymosan challenge. Enzyme activity was assayed using phenolphthalein glucuronic acid as substrate, with absorbance read at 540 nm. [1]
Nucleic acid binding affinity was assessed via absorption spectroscopy. Titrations of Hydroxystilbamidine (0–50 μM) into solutions of DNA/RNA (50 μM) monitored hypochromicity at 335 nm. Binding constants were calculated from Scatchard plots. [2] |
| Cell Assay |
Mouse peritoneal macrophages were harvested, cultured in medium, and pre-treated with Hydroxystilbamidine (1–10 μg/mL) for 30 min. Cells were then stimulated with zymosan particles (1 mg/mL) for 60 min. β-glucuronidase release in supernatants was measured to evaluate lysosomal membrane stability. [1]
For antifungal testing, Blastomyces dermatitidis was incubated with Hydroxystilbamidine (0.1–10 μg/mL) in broth culture at 37°C for 48 hours. Growth inhibition was determined by turbidity measurements at 600 nm. [1] |
| Animal Protocol |
Mice (CBA strain) received intraperitoneal injections of Hydroxystilbamidine (10 mg/kg dissolved in saline) daily for 4 days prior to immunization with sheep red blood cells. DTH response was evaluated by footpad swelling 24 hours after challenge. [1]
|
| References | |
| Additional Infomation |
Hydroxystilbene is a stilbene compound. Hydroxyethylstilbene is used to treat some patients with non-progressive dermatoblastomycosis and pulmonary or systemic blastomycosis in children, with fewer side effects than amphotericin B. Hydroxyethylstilbene is also used for pathological diagnosis. Hydroxystilbene is a cationic dye with antifungal, antitrypanosome, antimalarial, and anticancer activities. Hydroxystilbene binds to DNA and RNA in a non-intercalating manner and is a potent inhibitor of ribonucleases, thereby inhibiting cellular processes in protozoa. This drug has also been shown to bind to and stabilize trypanosome lysosomes. Hydroxystilbene is commonly used for neuroanatomical diagnosis and histochemical staining.
See also: Hydroxystilbene isothiocyanate (note moved to). Drug Indications For the treatment of non-progressive dermatoblastomycosis and other fungal infections. Mechanism of Action Hydroxystilbene isothiocyanate (HSB) acts on extracellular DNA and lysosomes. In trypanosomes, HSB binds extensively and selectively to kinetoplast DNA, thereby inhibiting cell division and reproduction. In yeast, there is evidence that HSB binds to extranuclear DNA, leading to a variety of mutations. HSB is also absorbed by lysosomes, resulting in a significant increase in the number of lysosomal-like bodies and secretory granules in trypanosomes. HSB may also stabilize lysosomal membranes. HSB has also been found to bind RNA and is a potent inhibitor of cellular ribonucleases. Hydroxystilbene, as a lysosomal stabilizer, inhibits the release of proteolytic enzymes, thereby suppressing immune cell activation and inflammatory responses. This mechanism is the basis for its immunosuppressive and antifungal effects. [1] This drug can serve as a unique non-intercalating nucleic acid probe because it selectively binds to guanine bases through hydrogen bonding and electrostatic interactions, thereby inducing conformational changes in double-stranded RNA and GC-rich DNA regions. [2] |
| Molecular Formula |
C16H16N4O
|
|---|---|
| Molecular Weight |
280.32
|
| Exact Mass |
280.132
|
| CAS # |
495-99-8
|
| Related CAS # |
223769-64-0
|
| PubChem CID |
5284571
|
| Appearance |
Typically exists as solid at room temperature
|
| Density |
1.288g/cm3
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| Boiling Point |
509.678ºC at 760 mmHg
|
| Melting Point |
235°
|
| Flash Point |
262.044ºC
|
| Vapour Pressure |
0mmHg at 25°C
|
| Index of Refraction |
1.654
|
| LogP |
1.578
|
| Hydrogen Bond Donor Count |
5
|
| Hydrogen Bond Acceptor Count |
3
|
| Rotatable Bond Count |
4
|
| Heavy Atom Count |
21
|
| Complexity |
413
|
| Defined Atom Stereocenter Count |
0
|
| SMILES |
C1=CC(=CC=C1/C=C/C2=C(C=C(C=C2)C(=N)N)O)C(=N)N
|
| InChi Key |
TUESWZZJYCLFNL-DAFODLJHSA-N
|
| InChi Code |
InChI=1S/C16H16N4O/c17-15(18)12-5-2-10(3-6-12)1-4-11-7-8-13(16(19)20)9-14(11)21/h1-9,21H,(H3,17,18)(H3,19,20)/b4-1+
|
| Chemical Name |
4-[(E)-2-(4-carbamimidoylphenyl)ethenyl]-3-hydroxybenzenecarboximidamide
|
| Synonyms |
HYDROXYSTILBAMIDINE; 495-99-8; 1071752-67-4; 4-[(E)-2-(4-carbamimidoylphenyl)ethenyl]-3-hydroxybenzenecarboximidamide; 4-(4-Carbamimidoylstyryl)-3-hydroxybenzimidamide; (E)-4-(4-carbamimidoylstyryl)-3-hydroxybenzimidamide; OHSA; NCGC00166289-01;
|
| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| Solubility (In Vitro) |
Typically soluble in DMSO (e.g. 10 mM)
|
|---|---|
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 3.5674 mL | 17.8368 mL | 35.6735 mL | |
| 5 mM | 0.7135 mL | 3.5674 mL | 7.1347 mL | |
| 10 mM | 0.3567 mL | 1.7837 mL | 3.5674 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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