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TP1012CH 5450CH5450,inhibit,MAB elastase 2,CH 5450,Inhibitor,Ang I,chymase,CH-5450
CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) is a short peptide inhibitor of chymase in the human heart
价 格：￥电议型 号：TP1012产 地：中国大陆
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T24488MLS000545091MLS 000545091；MLS-000545091
MLS000545091 is a potent and selective human epithelial 15-lipoxygenase-2 mixed-type inhibitor.
价 格：￥电议型 号：T24488产 地：中国大陆
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T5450DL-071-ITDL-071-IT,Afurolol Hydrochloride,DL 071 IT
DL 071-IT is a potent non-selective beta-adrenoceptor antagonist. DL 071 IT showed intrinsic sympathomimetic activity and weak membrane stabilizing activity.
价 格：￥电议型 号：T5450产 地：美洲
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T75450P-orlandin；化合物 P-orlandinP-orlandin
P-orlandin, a fungal metabolite, effectively impedes Plasmodium falciparum infection in mosquitoes by preventing FREP1 from binding to gametocytes or ookinetes [1].
价 格：￥电议型 号：T75450产 地：中国大陆
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T654505-Chloro-2-(methylamino)benzophenone；5-氯-2-(甲氨基)二苯甲酮5-Chloro-2-(methylamino)benzophenone
5-Chloro-2-(methylamino)benzophenone is a useful organic compound for research related to life sciences. The catalog number is T65450 and the CAS number is 1022-13-5.
价 格：￥电议型 号：T65450产 地：中国大陆
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T5450DL-071-IT；化合物DL-071-ITAfurolol Hydrochloride|||DL 071 IT；Afurolol Hydrochloride|||DL 071 IT
DL-071-IT (Afurolol Hydrochloride) is a potent non-selective beta-adrenoceptor antagonist. DL-071-IT showed intrinsic sympathomimetic activity and weak membrane stabilizing activity.
价 格：￥电议型 号：T5450产 地：中国大陆
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T35450α-GalCer analog 8；α-GalCer analog 8α-GalCer analog 8|||α-Galactosylceramide analog 8；α-GalCer analog
α-Galactosylceramide analog 8 (α-GalCer analog 8) is a triazole derivative of α-galactosylceramide. [1] It increases IL-2 secretion by DN32.D3 NKT hybridoma cells when co-cultured with CD1d-transfected RBL cells pre-loaded with α-GalCer analog 8 at a concentration of 32 ng/ml. α-GalCer analog 8 (32 ng/ml) induces IL-4 secretion to a greater extent than the synthetic α-GalCer KRN 7000 in mouse splenocytes in vitro and in mouse serum following administration of a 1 µg per animal dose, indicati
价 格：￥电议型 号：T35450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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T25450GGTI 2147；化合物GGTI 2147GGTI2147|||Geranylgeranyl transferase inhibitor-2147|||GGTI-2147；GGTI2147|||Ge
GGTI 2147 decreased Rac1 activity, down-regulated p65 expression, and ameliorated OGD/R-induced neuronal apoptosis.
价 格：￥电议型 号：T25450产 地：中国大陆
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T25371Emd 55450；化合物 T25371Emd55450|||Emd-55450；Emd55450|||Emd-55450
Emd 55450 is a synthetic renin antagonist. It is an analog of EMD 55068 with terminal amino group blocked by benzyloxycarbonyl group.
价 格：￥电议型 号：T25371产 地：中国大陆
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T24488MLS000545091；化合物 T24488MLS-000545091|||MLS 000545091；MLS-000545091|||MLS 000545091
MLS000545091 is a potent and selective human epithelial 15-lipoxygenase-2 mixed-type inhibitor.
价 格：￥电议型 号：T24488产 地：中国大陆
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T15450GW-803430；化合物 T15450GW-3430；GW-3430
GW-803430 is a potent and selective antagonist of melanin-concentrating hormone receptor 1 (MCH R1) (pIC50: 9.3). GW-803430 is orally active in an animal model of obesity.
价 格：￥电议型 号：T15450产 地：中国大陆
