Product Application:EH-IDTBR is a branched non-fullerene acceptor (NFAs) used in organic photovoltaic (OPV) devices. It is used along with donor polymer, poly (3-hexylthiophene) (P3HT) to fabricate the solar cells to enhance the power conversion
Product Application:EH-IDTBR is a branched non-fullerene acceptor (NFAs) used in organic photovoltaic (OPV) devices. It is used along with donor polymer, poly (3-hexylthiophene) (P3HT) to fabricate the solar cells to enhance the power conversion
Product Application:EH-IDTBR is a branched non-fullerene acceptor (NFAs) used in organic photovoltaic (OPV) devices. It is used along with donor polymer, poly (3-hexylthiophene) (P3HT) to fabricate the solar cells to enhance the power conversion
Product Application:EH-IDTBR is a branched non-fullerene acceptor (NFAs) used in organic photovoltaic (OPV) devices. It is used along with donor polymer, poly (3-hexylthiophene) (P3HT) to fabricate the solar cells to enhance the power conversion
InformationEmricasan (IDN-6556) Emricasan (IDN-6556, PF 03491390, PF-03491390) is a potent irreversible pan-caspase inhibitor. Emricasan is an inhibitor of Zika virus infection.In vitroEmricasan, also called IDN-6556 or PF-03491390, is an inhibitor
InformationEmricasan (IDN-6556) Emricasan (IDN-6556, PF 03491390, PF-03491390) is a potent irreversible pan-caspase inhibitor. Emricasan is an inhibitor of Zika virus infection.In vitroEmricasan, also called IDN-6556 or PF-03491390, is an inhibitor
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.
EMD 66684 is a potent, selective nonpeptide AT1 receptor antagonist. This compound prevents the binding of angiotensin II to the receptor, which blocks the signal cascade that induces vasoconstricition.