Lappaconite Hydrobromide 100mg 100mg | Purity Not Available
Adooq Bioscience
Lappaconite Hydrobromide is a kind of alkaloid extracted from Aconitum sinomontanum Nakai and has anti-inflammatory effects.
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Lappaconite Hydrobromide 10mg 10mg | Purity Not Available
Adooq Bioscience
Lappaconite Hydrobromide is a kind of alkaloid extracted from Aconitum sinomontanum Nakai and has anti-inflammatory effects.
More Information Supplier PageLapatinib Ditosylate 50mg 50mg | Purity Not Available
Adooq Bioscience
Lapatinib is a dual tyrosine kinase inhibitor which interrupts the HER2 growth receptor pathway.
More Information Supplier PageLapatinib Ditosylate 25mg 25mg | Purity Not Available
Adooq Bioscience
Lapatinib is a dual tyrosine kinase inhibitor which interrupts the HER2 growth receptor pathway.
More Information Supplier PageLapatinib Ditosylate 200mg 200mg | Purity Not Available
Adooq Bioscience
Lapatinib is a dual tyrosine kinase inhibitor which interrupts the HER2 growth receptor pathway.
More Information Supplier PageKU-55933 5mg 5mg | Purity Not Available
Adooq Bioscience
KU-55933 is an ATM inhibitor by suppressing cell proliferation and induces apoptosis by blocking Akt in cancer cells with overactivated Akt.
More Information Supplier PageKU-55933 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
KU-55933 is an ATM inhibitor by suppressing cell proliferation and induces apoptosis by blocking Akt in cancer cells with overactivated Akt.
More Information Supplier PageKU-55933 100mg 100mg | Purity Not Available
Adooq Bioscience
KU-55933 is an ATM inhibitor by suppressing cell proliferation and induces apoptosis by blocking Akt in cancer cells with overactivated Akt.
More Information Supplier PageKU-55933 10mg 10mg | Purity Not Available
Adooq Bioscience
KU-55933 is an ATM inhibitor by suppressing cell proliferation and induces apoptosis by blocking Akt in cancer cells with overactivated Akt.
More Information Supplier PageKU-0063794 50mg 50mg | Purity Not Available
Adooq Bioscience
KU-0063794 is a selective inhibitor of mammalian target of rapamycin (mTOR) (IC50 ~10 nM for mTORC1 and mTORC2 respectively).
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