Miransertib (ARQ 092) HCl

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Reagent Code: #101414
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CAS Number 1313883-00-9

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Weight 468.98 g/mol
Formula C₂₇H₂₅ClN₆
inventory_2 Storage & Handling
Storage -20℃

description Product Description

Miransertib (ARQ 092) HCl is primarily used in the field of oncology as a targeted therapy for the treatment of cancers associated with mutations in the AKT1 gene. It functions as an AKT inhibitor, effectively blocking the PI3K/AKT/mTOR signaling pathway, which is often hyperactive in various cancers. This inhibition helps to reduce tumor growth and progression, making it a promising option for patients with specific genetic mutations. Additionally, it is being explored for its potential in treating Proteus syndrome, a rare overgrowth disorder caused by AKT1 mutations. Its ability to selectively target abnormal cellular pathways offers a more precise and potentially less toxic treatment approach compared to traditional chemotherapy.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿6,642.00

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Miransertib (ARQ 092) HCl
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Miransertib (ARQ 092) HCl is primarily used in the field of oncology as a targeted therapy for the treatment of cancers associated with mutations in the AKT1 gene. It functions as an AKT inhibitor, effectively blocking the PI3K/AKT/mTOR signaling pathway, which is often hyperactive in various cancers. This inhibition helps to reduce tumor growth and progression, making it a promising option for patients with specific genetic mutations. Additionally, it is being explored for its potential in treating Prot

Miransertib (ARQ 092) HCl is primarily used in the field of oncology as a targeted therapy for the treatment of cancers associated with mutations in the AKT1 gene. It functions as an AKT inhibitor, effectively blocking the PI3K/AKT/mTOR signaling pathway, which is often hyperactive in various cancers. This inhibition helps to reduce tumor growth and progression, making it a promising option for patients with specific genetic mutations. Additionally, it is being explored for its potential in treating Proteus syndrome, a rare overgrowth disorder caused by AKT1 mutations. Its ability to selectively target abnormal cellular pathways offers a more precise and potentially less toxic treatment approach compared to traditional chemotherapy.

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