Ethyl 3-(2-(((4-carbamimidoylphenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate acetate

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Reagent Code: #182784
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CAS Number 1188263-64-0

science Other reagents with same CAS 1188263-64-0

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Weight 559.62 g/mol
Formula C₂₉H₃₃N₇O₅
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of factor Xa inhibitors, which are anticoagulant drugs designed to prevent blood clot formation. It plays a role in developing treatments for cardiovascular diseases such as deep vein thrombosis, pulmonary embolism, and stroke. The compound's structure enables selective interaction with serine proteases, enhancing drug specificity and reducing bleeding risks compared to traditional anticoagulants. Also investigated for improved bioavailability and metabolic stability in oral dosage forms.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,050.00
inventory 1g
10-20 days ฿10,300.00

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Ethyl 3-(2-(((4-carbamimidoylphenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate acetate
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Used in pharmaceutical research as a key intermediate in the synthesis of factor Xa inhibitors, which are anticoagulant drugs designed to prevent blood clot formation. It plays a role in developing treatments for cardiovascular diseases such as deep vein thrombosis, pulmonary embolism, and stroke. The compound's structure enables selective interaction with serine proteases, enhancing drug specificity and reducing bleeding risks compared to traditional anticoagulants. Also investigated for improved bioava

Used in pharmaceutical research as a key intermediate in the synthesis of factor Xa inhibitors, which are anticoagulant drugs designed to prevent blood clot formation. It plays a role in developing treatments for cardiovascular diseases such as deep vein thrombosis, pulmonary embolism, and stroke. The compound's structure enables selective interaction with serine proteases, enhancing drug specificity and reducing bleeding risks compared to traditional anticoagulants. Also investigated for improved bioavailability and metabolic stability in oral dosage forms.

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