(R)-Carisbamate

95%

Reagent Code: #37260
fingerprint
CAS Number 194085-74-0

science Other reagents with same CAS 194085-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.6336 g/mol
Formula C₉H₁₀ClNO₃
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(R)-Carisbamate (C9H10N2O3, MW 194.19) is a chiral synthetic organic compound and specialty research chemical (≥95% purity). It was investigated as a potential anticonvulsant for epilepsy and other CNS disorders due to its ability to modulate neuronal excitability via a unique mechanism distinct from other antiepileptic drugs. It also showed promise in preclinical studies for neuropathic pain relief and neuroprotection in conditions like stroke or neurodegenerative diseases. Although clinical development was discontinued by Johnson & Johnson in 2009 after phase III trials failed to demonstrate sufficient efficacy, it remains valuable in laboratory research for refractory epilepsy models, pain signaling pathways, and neuroprotective studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,130.00
inventory 1g
10-20 days ฿11,180.00
inventory 100mg
10-20 days ฿1,580.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-Carisbamate
No image available

(R)-Carisbamate (C9H10N2O3, MW 194.19) is a chiral synthetic organic compound and specialty research chemical (≥95% purity). It was investigated as a potential anticonvulsant for epilepsy and other CNS disorders due to its ability to modulate neuronal excitability via a unique mechanism distinct from other antiepileptic drugs. It also showed promise in preclinical studies for neuropathic pain relief and neuroprotection in conditions like stroke or neurodegenera

(R)-Carisbamate (C9H10N2O3, MW 194.19) is a chiral synthetic organic compound and specialty research chemical (≥95% purity). It was investigated as a potential anticonvulsant for epilepsy and other CNS disorders due to its ability to modulate neuronal excitability via a unique mechanism distinct from other antiepileptic drugs. It also showed promise in preclinical studies for neuropathic pain relief and neuroprotection in conditions like stroke or neurodegenerative diseases. Although clinical development was discontinued by Johnson & Johnson in 2009 after phase III trials failed to demonstrate sufficient efficacy, it remains valuable in laboratory research for refractory epilepsy models, pain signaling pathways, and neuroprotective studies.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...