toxina

(±)-Anatoxin A fumarate是(±)-Anatoxin A的盐形式。(±)-Anatoxin A是具有强烈的神经毒性的天然生物碱，被称为快速死亡因子（VFDF），是一种强效、直接和选择性的nAchR（烟碱乙酰胆碱受体）激动剂，也称为nicotinic receptor（烟碱受体）激动剂。

(±)-Anatoxin A hydrochloride是(±)-Anatoxin A的盐形式。(±)-Anatoxin A是具有强烈的神经毒性的天然生物碱，被称为快速死亡因子（VFDF），是一种强效、直接和选择性的nAchR（烟碱乙酰胆碱受体）激动剂，也称为nicotinic receptor（烟碱受体）激动剂。

β-Pompilidotoxin Acetate 是一种黄蜂毒肽。 它可以减缓钠通道的失活并增加细胞中的稳态钠电流。

Ceratotoxin A acetate 是从副腺分泌液中分离出来的，具有抗菌作用。

Hymatoxin A 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126421，CAS号为 109621-33-2。

Roritoxin A 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126507，CAS号为 102852-48-2。

Lanceotoxin A is a potent Ip blocker.

Rubratoxin A is a classical mycotoxin used as a PP2A-specific inhibitor.

Valyl-ochratoxin A is a phenylalanyl moiety of ochratoxin A replaced by valine. It is a yeast valyl-tRNA synthetase inhibitor.

Apratoxin A is a potent cytotoxin isolated from the marine cyanobacterium Lyngbya majuscula Harvey ex Gomont.

Holotoxin A1 is a bioactive chemical.

Lyngbyatoxin A is an indole alkaloid from blue-green alga Lyngbya majuscula Gomont; responsible for dermatitis known as "swimmers' itch" in Hawaii.

Ochratoxin A-13C20is intended for use as an internal standard for the quantification of ochratoxin A by GC- or LC-MS. Ochratoxin A is a mycotoxin that has been found inAspergillusandPenicillium.1It increases lipid peroxide levels and the number of apoptotic cells, as well as reduces superoxide dismutase activity in rat kidney when administered at a dose of 120 μg kg.2Topical application of ochratoxin A (80 μg mouse) induces DNA damage, cell cycle arrest at the G0 G1phase, and apoptosis in mouse skin cells.1It also initiates tumor formation in a two-stage mouse skin tumorigenesis model. Ochratoxin A has been found as a contaminant in a variety of foods.3

Muscotoxin A is an ADC cytotoxin with lipopeptide properties that effectively permeabilizes mammalian cell membranes, ultimately inducing necrotic cell death.

Ochratoxin α (Ochratoxin alpha)是一种 Ochratoxin A 的降解产物，可用于研究 Ochratoxin A 降解。

Makaluvamine A comes from the fruiting bodies of Didymium bahiense that act as active anti-cancer agents and DNA topo II inhibitors.

α-Conotoxin AuIB TFA，一种选择性α3β4烟碱乙酰胆碱受体(nAChR)的有效拮抗剂，能阻断在非洲爪蟾卵母细胞中表达的α3β4 nAChRs，其IC50值为0.75 μM。

Actoxumab 是一种针对艰难梭菌毒素 A (C. difficile toxin A) 的人源化单克隆抗体，阻止 TcdA 与靶细胞的结合，通过抑制 TcdA 的第一步来中和毒素活性。

Imperatoxin A，源自非洲蝎Pandinus imperator毒液的一种肽毒素，作为Ca2+-释放通道 兰尼碱受体（RyRs）的激活剂，促进Ca2+从肌浆网流入细胞。

α-Conotoxin AuIA为高效的α3β4 nAChR选择性抑制剂，源自Conus aulicus的分离提取。

Spinoxin是一种从Heterometrus spinifer蝎子毒液中提取的神经毒素，由34个氨基酸残基组成，通过4个二硫桥交联。它能有效抑制Kv1.3钾通道（IC50= 63 nM），是研发诊断及治疗自身免疫性疾病和癌症策略时的潜在分子靶点。

Anatoxin-a (ATX-a), a neurotoxic alkaloid, functions as an agonist for the nicotinic acetylcholine receptor (nAChR) and as an inhibitor of Acetylcholinesterase (AChE) [1] [2].

Sapintoxin A, 一种从Sapium indicum的未成熟果实中提取的佛波醇酯。

7,14-Epoxymeliatoxin A1 是一种天然产物，可用作天然产物对照品，用于生命科学相关领域的研究，其产品编号为 TN8540。