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Cat. No. | Product Name | Target | Signaling Pathways |
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T82213 |
Herbicidal agent 1
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Herbicidal agent 1((S)-6q)是一种活性高于相应外消旋体的除草剂。 | |||
T19857 |
Glyphosate
Atila,Lancer,Folusen,草甘膦 |
Apoptosis; Autophagy | Apoptosis; Autophagy |
Glyphosate (Atila) 是氨基酸甘氨酸的衍生物。它是一种除草剂,靶向并阻断植物合成芳香氨基酸所必需的莽草酸途径。 | |||
T19369 |
Imazapic
甲咪唑烟酸,Imazamethapyr |
Others | Others |
Imazapic (Imazamethapyr) 具有广泛的除草谱,可防治多种一年生禾本科杂草。 | |||
T25950 |
Phosalacine
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Phosalacine, isolated from Kitasatosporia phosalacinea, is a new herbicidal antibiotic that contains phosphinothricin. | |||
T74695 | Antimalarial agent 17 | ||
Antimalarial agent 17,一种兼具抗疟和除草功能的化合物,作为光系统 II 型抑制剂,在出苗后除草活性方面与市售除草剂表现出相当的效力。 | |||
T81415 |
PPO-IN-3
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PPO-IN-3(Compound 8ad)是一种高效的PPO抑制剂,具有0.67 nM的KI值,并表现出显著的芽后除草活性,主要用于杂草控制。 | |||
T81471 |
Phytoene desaturase-IN-2
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PDS-IN-1为Oryza sativa中八氢番茄红素去饱和酶(OsPDS)的抑制剂,具备除草效能。 | |||
T74981 | Transketolase-IN-3 | ||
Transketolase-IN-3为有效的转酮酶(TK)抑制剂,展现出杰出的除草活性,并对血红木(DS)及苋菜(AR)显示出抑制效果,适用于研究除草剂。 | |||
T60614 |
DHDPS-IN-1
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DHDPS-IN-1 (compound 8) 是二氢吡啶二羧酸合酶 (DHDPS)的抑制剂,IC50值为 39 μM,可用于抗菌和除草领域。 | |||
T79338 |
HPPD-IN-1
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HPPD-IN-1 (compound II-3)为一种有效的HPPD抑制剂,其对拟南芥HPPD (AtHPPD)的IC50为0.248 μM,表现出优于mesotrione的抑制效果(其IC50为0.283 μM)。此外,HPPD-IN-1对阔叶和单子叶杂草均展现出杰出的除草性能。 | |||
T74929 | Phytoene desaturase-IN-1 | ||
Phytoene desaturase-IN-1 是高效的PDS抑制剂(Kd: 65.9 μM),通过与Phe301残基形成π-π堆叠效应。该化合物显示出广谱的芽后除草活性,并能在白化病叶片中诱导PDS mRNA水平下降及八氢番茄红素与ROS累积,适用于农业生产。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T83551 |
(9S)-Macrocidin B
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(9S)-Macrocidin B 的除草活性不如macrocidin A。 | |||
T82822 |
Brassicanate A sulfoxide
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Brassicanate A sulfoxide 表现出除草效果,它能抑制植物中必需氨基酸的生物合成路径。该化合物通过结合并抑制多种酶的活性来发挥其作用,包括二羟酸脱水酶 (DHAD)、羟甲基丙酮酸双加氧酶 (HPPD)、乙酰乳酸合酶 (ALS)、PYL家族蛋白及转运抑制剂响应 1 (TIR1)。Brassicanate A sulfoxide 可以从甘蓝 (Brassica oleracea) 中提取获得。 | |||
T36749 |
Herboxidiene
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Herboxidiene is a polyketide originally isolated from S. chromofuscus that has diverse biological activities.[1],[2,][3],[4],[5] It inhibits growth of HeLa S3, SK-MEL-2, PC3, A549, and EBC-1 cells with GI50 values ranging from 7.4 to 62 nM.3 Herboxidiene is cytostatic against human umbilical vein endothelial cells (HUVECs; (IC50 = 26 nM)) and inhibits VEGF-induced invasion and tube formation of serum-starved HUVECs in a concentration-dependent manner, indicating antiangiogenic activity.[4] Herbo... |