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Cat. No. | Product Name | Target | Signaling Pathways |
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TP1289 |
Cardiotoxin Analog (CTX) IV (6-12) TFA
Cardiotoxin Analog (CTX) IV (6-12) (TFA)(115722-23-1,FREE) |
Others | Others |
Cardiotoxin Analog (CTX) IV (6-12) TFA(115722-23-1 free base) 是 Cardiotoxin Analog (CTX) IV 的部分肽。从台湾眼镜蛇毒液中分离出的心脏毒素类似物 IV。 CTX IV 是一种独特的蛇毒心脏毒素。 | |||
T26212 |
SQ 20858
SQ 20,858,SQ20858,SQ-20858,SQ-20,858,SQ20,858 |
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SQ 20858 is a synthetic peptide derived from snake Bothrops jararaca venom; suppresses angiotensin serum converting enzyme. | |||
T80468 |
δ-Dendrotoxin
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Potassium Channel | Membrane transporter/Ion channel |
δ-Dendrotoxin,作为一种K+通道阻滞剂,来源于黑曼巴蛇的毒液,常用于研究神经系统疾病。 | |||
T81787 |
MitTx-beta
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MitTx-beta为一多肽,源自得克萨斯珊瑚蛇(Micrurus tener tener)之毒液。与MitTx-α配对,组成复合物MitTx,此复合物激活ASIC1通道,存在于辣椒素敏感神经纤维上。 | |||
T80064 |
Dendrotoxin-I
DTX-I |
Potassium Channel | Membrane transporter/Ion channel |
Dendrotoxin-I是一种高效的K+通道阻滞剂,特异性针对KV1.1和KV1.2电压门控钾通道亚基。该化合物为从Dendroaspis蛇毒中提取的神经毒素。 | |||
T75582 | Naja Melanoleuca Venom | ||
Naja Melanoleuca Venom (Forest Cobra Venom) 是一种蛇毒,可从 Naja Melanoleuca 获得。Naja Melanoleuca Venom 对人类红细胞具有溶血活性。α-神经毒素可以从 Naja Melanoleuca 毒液中分离出来,并抑制 GABAA 受体功能。 | |||
T75408 | Batroxobin | ||
Batroxobin (DF-521),一种从Bothrops atrox moojeni获得的蛇毒,能促进血栓溶解,防止血栓复发并具有神经保护作用,显示出在脑静脉血栓性疾病研究中的潜力。 | |||
T80487 |
MmTx2 toxin
Micrurotoxin 2 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
MmTx2 toxin作为一种GABAA受体调节剂,具有提升GABAA受体对激动剂反应敏感性的作用。该毒素来源于珊瑚蛇的毒液,并在神经系统相关疾病(例如癫痫、精神分裂症及慢性疼痛)的研究中发挥重要用途。 | |||
T75585 | Naja Mossambica Venom | ||
Naja Mossambica Venom (Mozambique Spitting Cobra Venom) 是一种蛇毒,可从 Naja Mossambica 获得。Naja Pallida Venom 对Candida 物种具有抗真菌活性。Naja Mossambica Venom 提取物 (如磷脂酶 A2) 可抑制钠钾 ATP 酶活性。 | |||
T75589 | Bitis Cornuta Venom | ||
Bitis Cornuta Venom (Many-horned Adder Venom) 是从 Bitis Cornuta 提取的蛇毒,含有sPLA2毒素,该毒素具有通过抑制凝血酶原复合物以发挥抗凝活性的能力,并能促使凝血酶原转化为凝血酶,引发凝块形成。 | |||
T37832 |
CAY10761
CAY10761 |
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CAY10761 is an inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; IC50s = 467 and 429 μM for the human and snake venom enzymes, respectively).1,2 It also inhibits mushroom tyrosinase (Ki = 1.9 μM) and urease from jack bean, P. mirabilis, and B. pasteurii (IC50s = 0.093, <0.125, and 0.089 mM, respectively, at pH 8.2).3,4 |1. Khan, K.M., Fatima, N., Rasheed, M., et al. 1,3,4-Oxadiazole-2(3H)-thione and its analogues: A new class of non-competitive nucleotide pyrophosphatases/p... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN1788 |
Isookanin
|
Amylase | Metabolism |
Isookanin 在多种疾病领域有研究价值,包括肿瘤,皮疹,蛇和昆虫叮咬,糖尿病,腹泻。它可作为抗病毒剂对抗 HSV 和水痘带状疱疹病毒。它也具有抗氧化特性。 | |||
TN4886 | Quinovic acid 3-O-alpha-L-rhamnopyranoside | Others | Others |
Quinovic acid 3-O-alpha-L-rhamnopyranoside shows significant inhibitory activity against snake venom phosphodiesterase-I. | |||
TN4247 | Ikshusterol 3-O-glucoside | Phospholipase | Metabolism |
Ikshusterol 3-O-glucoside has a potent snake-venom neutralizing capacity and it might be a potential molecule for the therapeutic treatment for snakebites. | |||
T36295 | Echistatin TFA | ||
Echistatin TFA, the smallest active RGD protein belonging to the family of disintegrins that are derived from snake venoms, is a potent inhibitor of platelet aggregation. Echistatin is a potent inhibitor of bone resorption in culture. Echistatin is a potent antagonist of αIIbβ3, αvβ3 and α5β1[1][2][3][4]. [1]. J Musial, et al. Inhibition of platelet adhesion to surfaces of extracorporeal circuits by disintegrins. RGD-containing peptides from viper venoms. Circulation. 1990 Jul;82(1):261-73.[2]. ... |