PeptideDB

Naftazone 15687-37-3

Naftazone 15687-37-3

CAS No.: 15687-37-3

Naftazone (Etioven) is a novel and potent vasoprotectant drug used for hemostasis. It can accelerate human saphenous vei
Data collection:peptidedb@qq.com

This product is for research use only, not for human use. We do not sell to patients.

Naftazone (Etioven) is a novel and potent vasoprotectant drug used for hemostasis. It can accelerate human saphenous vein endothelial cell proliferation in vitro at concentrations which did not alter the hemostatic balance.



Physicochemical Properties


Molecular Formula C11H9N3O2
Molecular Weight 215.212
Exact Mass 215.069
CAS # 15687-37-3
PubChem CID 71688
Appearance Yellow to orange solid powder
Density 1.4g/cm3
Index of Refraction 1.678
LogP 2.011
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Heavy Atom Count 16
Complexity 293
Defined Atom Stereocenter Count 0
SMILES

NC(N/N=C1\C=CC2=CC=CC=C2C\1=O)=O

InChi Key AGSIRJFXAANBMW-UHFFFAOYSA-N
InChi Code

InChI=1S/C11H9N3O2/c12-11(16)14-13-9-6-5-7-3-1-2-4-8(7)10(9)15/h1-6,15H,(H2,12,16)
Chemical Name

(1-hydroxynaphthalen-2-yl)iminourea
Synonyms

C05CX02 Etioven Naftazone
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)

Biological Activity


ln Vitro In mouse cerebellar synaptosomes, naftazone (0.5-50 μM; 1 h) decreases glutamate release[1].
ln Vivo The glutamate content of the cerebrospinal fluid is impacted by naftazone (10 and 100 mg/kg; po once daily for 15 days)[1]. Rats' platelet function is impacted by naftazone (50 mg/kg; intraperitoneally once daily for five days)[2].
Animal Protocol Animal/Disease Models: Male rats[1]
Doses: 10 and 100 mg/kg
Route of Administration: po (oral gavage); 10 and 100 mg/kg once per day; for 15 days
Experimental Results: Dramatically decreased glutamate content in cerebro spinal fluid of rats.

Animal/Disease Models: Wistar rats[2]
Doses: 50 mg/kg
Route of Administration: intraperitoneal (ip)injection ; 50 mg/kg one time/day for 5 days
Experimental Results: decreased the height of platelet aggregation induced by ADP, Dramatically increased the platelet disaggregation induced by collagen and decreased fibrinogen binding to 2.5 or 5 μM ADP-stimulated platelet.
References

[1]. Naftazone reduces glutamate cerebro spinal fluid levels in rats and glutamate release from mouse cerebellum synaptosomes. Neurosci Lett. 1999 Aug 27;271(3):183-6.

[2]. Effect of naftazone on in vivo platelet function in the rat. Platelets. 1999;10(1):66-70.

Additional Infomation Naftazone is a member of naphthalenes.

Solubility Data


Solubility (In Vitro) May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*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).
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)]
*Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300:Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL 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).
Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders

Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 4.6466 mL 23.2331 mL 46.4662 mL
5 mM 0.9293 mL 4.6466 mL 9.2932 mL
10 mM 0.4647 mL 2.3233 mL 4.6466 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.