Products for Research Use Only

Idramantone

CAT: 0804-HY-B1044-01Size: 100 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0804-HY-B1044-01Size:100 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Idramantone (Kemantane, 5-Hydroxy-2-adamantanone) is an Adamantane derivative. Idramantone is an immunostimulant. Idramantone is a versatile starting material for the synthesis of various adamantine deivatives. Idramantone can be produced using P450cam monooxygenase coupled with NADH regeneration as an oxidation biocatalyst. Idramantone can be studied in research on bronchial pathology[1][2][3].
CAS Number
20098-14-0
Product Name Alternative
Kemantane; 5-Hydroxy-2-adamantanone
UNSPSC
12352211
Hazard Statement
H302, H315, H319, H335
Target
Drug Derivative
Type
Reference compound
Related Pathways
Others
Applications
Neuroscience-Neuromodulation
Field of Research
Inflammation/Immunology; Neurological Disease
Assay Protocol
https://www.medchemexpress.com/Idramantone.html
Concentration
10mM
Purity
99.94
Solubility
H2O : 20 mg/mL (ultrasonic)
Smiles
O=C1C(C2)CC3CC2(O)CC1C3
Molecular Formula
C10H14O2
Molecular Weight
166.22
Precautions
H302, H315, H319, H335
References & Citations
[1]Boĭko SS, et al. Mezhvidovye razlichiia farmakokinetiki kemantana [Interspecific differences in kemantan pharmacokinetics]. Eksp Klin Farmakol. 1994;57 (6) :48-50.|[2]Boĭko SS, et al., The clinical pharmacokinetics of kemantane. Farmakologiia i Toksikologiia, 01 Jan 1991, 54 (1) :57-59.|[3]Toshiki Furuya, et al., Biocatalytic production of 5-hydroxy-2-adamantanone by P450cam coupled with NADH regeneration, Journal of Molecular Catalysis B: Enzymatic, 2013, 94:111-118.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched

Alternative Products