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T72058LCDD-1102 HCl；CDD-1102盐酸盐CDD-1102 HCl(2757619-84-2 Free base)；CDD-1102 HCl(2757619-84-2 Free base)
CDD-1102 HCl is a novel BRDT-BD4 / BRD2-BD1302 selective inhibitor that shows non-hormonal contraceptive potential in ex vivo experiments.
价 格：￥电议型 号：T72058L产 地：中国大陆
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T71102CFG920；化合物 CFG920CFG920
CFG920 is a CYP17 inhibitor, is also an orally available inhibitor of the steroid 17-alpha-hydroxylase/C17,20 lyase (CYP17A1 or CYP17), with potential antiandrogen and antineoplastic activities. Upon oral administration, CYP17 inhibitor CFG920 inhibits the enzymatic activity of CYP17A1 in both the testes and adrenal glands, thereby inhibiting androgen production. This may decrease androgen-dependent growth signaling and may inhibit cell proliferation of androgen-dependent tumor cells.
价 格：￥电议型 号：T71102产 地：中国大陆
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T61102HIF-1/2α-IN-2；化合物 HIF-1/2α-IN-2HIF-1/2α-IN-2
HIF-1/2α-IN-2 is a potent inhibitor of HIF-1/2α, which effectively reduces the levels of HIF-1/2α. This compound elicits an iron starvation response by specifically targeting ISCA2, a key protein involved in Iron Sulfur Cluster Assembly 2. [1]
价 格：￥电议型 号：T61102产 地：中国大陆
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T4S1102Liensinine diperchlorate；莲心碱高氯酸盐Liensinine-Perchlorate；莲心碱高氯酸盐|||莲心碱二高氯酸盐|||Liensinine-Perchlorate
Liensinine Diperchlorate is an isoquinoline alkaloid extracted from the embryonic seeds of the sacred lotus. It inhibits late autophagy by blocking autophagosome-lysosome fusion and exhibits biological activities such as anti-arrhythmic, anti-hypertensive, anti-pulmonary fibrosis, and vascular smooth muscle relaxation.
价 格：￥电议型 号：T4S1102产 地：中国大陆
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T4497LAmifampridine phosphate；化合物 T4497LBRN0110232|||3,6-DAP|||SC10|||BRN 0110232|||BRN-0110232|||NSC 5217
Amifampridine is mainly used to treat many rare muscle diseases. In the United States, aminopyridine is being studied for the treatment of Lambert-Eaton myasmus syndrome (LEMS). Amifampridine is also used to treat many congenital myasthenia syndromes, particularly those with defects in choline acetyltransferase, downstream kinase 7, and any type of defects leading to "fast track" defects.
价 格：￥电议型 号：T4497L产 地：中国大陆
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T4294NS 11021；化合物NS11021NS11021；NS11021
NS 11021 (NS11021) , a novel opener of large-conductance Ca(2+)-activated K(+) channels
价 格：￥电议型 号：T4294产 地：中国大陆
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T41102BSc3094；BSc3094BSc3094
BSc3094 is a potent Tau aggregation inhibitor that demonstrates the potential for Alzheimer´s disease (AD) research.
价 格：￥电议型 号：T41102产 地：中国大陆
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T31102Cryptopine；化合物 T31102NSC32984|||Kryptocavin|||Cryptocavine|||Kryptopine|||Cryptopin；NSC32984|||Krypt
Cryptopine in vivo disturbs the cellular defense system, so that it tips in the direction of autoxidative lipid peroxidation, producing cytotoxicity.
价 格：￥电议型 号：T31102产 地：中国大陆
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T27590IHVR-11029；化合物 T27590IHVR 11029；IHVR 11029
IHVR-11029 is a potent inhibitor of ER α-glucosidase. IHVR-11029 is active against multiple hemorrhagic fever viruses and efficiently disrupts the morphogenesis of a broad spectrum of enveloped viruses.
价 格：￥电议型 号：T27590产 地：中国大陆
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T2710TCS 1102；化合物TCS 1102DORA-1；DORA-1
TCS 1102 is an effective, dual orexin receptor antagonist (Ki: 0.2/3 nM for OX2/1 receptors).
价 格：￥电议型 号：T2710产 地：中国大陆
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T26645Aptiganel；阿替加奈CNS 1102|||CNS-1102|||CNS1102；CNS 1102|||CNS-1102|||CNS1102
Aptiganel (CNS-1102) is a non-competitive NMDA antagonist, a peptide that may be used to study acute ischemic stroke.
价 格：￥电议型 号：T26645产 地：中国大陆
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T25450LGGTI 2147 FA；GGTI 2147甲酸盐GGTI2147 FA|||GGTI-2147 FA|||GGTI 2147 FA(191102-87-1 Free base)；GGTI2147 F
GGTI 2147 FA, a selective GGT inhibitor, abolishes bicuculline-induced increase in dendritic spine density in hippocampal experiments and may reduce learning and memory abilities in mice.
价 格：￥电议型 号：T25450L产 地：中国大陆
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T25221Cefaparole；化合物 T25221Cefaparol|||Lilly 110264|||Lilly-110264|||Lilly110264|||Cefaparolum；Cefaparol||
Cefaparole is an antibacterial compound and cell wall biosynthesis inhibitor.
价 格：￥电议型 号：T25221产 地：中国大陆
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T21102L-4FPG；L-4-氟苯甘氨酸L4FPG|||L 4FPG；L-4-氟苯甘氨酸|||L4FPG|||L 4FPG
L-4FPG is a Glycine derivative, inhibits the neutral amino acid transporters ASCT1 and ASCT2.
价 格：￥电议型 号：T21102产 地：中国大陆
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T11029hDHODH-IN-5；化合物hDHODH-IN-5DHODH-IN-7；DHODH-IN-7
hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH, IC50 = 0.91 μM).
价 格：￥电议型 号：T11029产 地：中国大陆
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T11028hDHODH-IN-4；化合物hDHODH-IN-4DHODH-IN-5；DHODH-IN-5
hDHODH-IN-4 (DHODH-IN-5) is a potent inhibitor of human dihydrogen dehydrogenase (DHODH). For human recombinant DHODH, its pIC50 is 7.8. hDHODH-IN-4 inhibits measles virus replication with a pMIC50 of 8.8.
价 格：￥电议型 号：T11028产 地：中国大陆
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T11027DHODH-IN-4；化合物DHODH-IN-4DHODH-IN-4
DHODH-IN-4 is a human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) inhibitor. The IC50 values of PfDHODH and HsDHODH are 4 μM and 0.18 μM, respectively. DHODH-IN-4 has antimalarial activity.
价 格：￥电议型 号：T11027产 地：中国大陆
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T11026DHODH-IN-3；化合物 T11026DHODH-IN-3
DHODH-IN-3 is an effective inhibitor of human dihydroorotate dehydrogenase (HsDHODH) with IC50 value of 261 nM. DHODH-IN-3 binds to the ubiquinone binding cavity in DHODH with a Kiapp of 32 nM. DHODH-IN-3 has the potential to treat malaria.
价 格：￥电议型 号：T11026产 地：中国大陆
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T11025hDHODH-IN-3；化合物hDHODH-IN-3DHODH-IN-2；DHODH-IN-2
hDHODH-IN-3 is an inhibitor of human dihydroorotate dehydrogenase with a pMIC50 value of 8.6. hDHODH-IN-3 can inhibit measles virus replication.
价 格：￥电议型 号：T11025产 地：中国大陆
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T11024DHODH-IN-15；化合物DHODH-IN-15DHODH-IN-15
DHODH-IN-15 is the hydroxyfuran analogue of A771726. DHODH-IN-15 is a dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 11 μM for rat liver DHODH. DHODH-IN-15 can be used for rheumatoid arthritis.
价 格：￥电议型 号：T11024产 地：中国大陆
