[CAS NO. 73963-62-9]  3,4-DehydroCilostazol

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PRODUCTS SPECIFICATIONS [73963-62-9]

Catalog
HY-135910
Brand
MCE
CAS
73963-62-9

DESCRIPTION [73963-62-9]

Overview

MDLMFCD08063649
Molecular Weight367.44
Molecular FormulaC20H25N5O2
SMILESO=C1NC2=C(C=C(OCCCCC3=NN=NN3C4CCCCC4)C=C2)C=C1

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

Summary

3,4-Dehydro Cilostazol (OPC-13015) is an active metabolite of Cilostazol (CLZ; HY-17464). 3,4-Dehydro Cilostazol is used for pharmacokinetic study [1] .


In Vivo

3,4-Dehydro Cilostazol (OPC-13015; Oral; 1 mg/kg GLZ and 10 mg/kg CLZ) has a T 1/2 of 3.94 hours, a C max of 1.39 μM and an AUC 0-24 of 4.69 μg•h/ml. The plasma concentration time profiles of GLZ, CLZ & its active metabolite DCLZ are traceable up to 24 h, 12 h and 12 h respectively by oral administration at 1 mg/kg dose of GLZ and 10 mg/kg CLZ [1] .

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

Animal Model: Male Wistar rats weighing 200 g [1]
Dosage: 1 mg/kg Glipizide (GLZ) and 10 mg/kg Cilostazol (CLZ) (Pharmacokinetic Analysis)
Administration: Oral
Result: Had a T 1/2 of 3.94 hours, a C max of 1.39 μM and an AUC 0-24 of 4.69 μg•h/ml.

Appearance

Solid


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

Solvent & Solubility

In Vitro:

DMSO : 5 mg/mL ( 13.61 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.7215 mL 13.6077 mL 27.2153 mL
5 mM 0.5443 mL 2.7215 mL 5.4431 mL
10 mM 0.2722 mL 1.3608 mL 2.7215 mL
* Please refer to the solubility information to select the appropriate solvent.