reversal

Sugammadex sodium (Org25969) 是合成的 γ 环糊精衍生物，是一种新型的神经肌肉阻断逆转剂。

Resorcinolnaphthalein 是一种特异性的血管紧张素转换酶 2 激活剂，EC50=19.5 μM。Resorcinolnaphthalein 能够用于高血压和肾纤维化的研究

Rubone（2'-羟基-2,4,4',5,6'-五甲氧基查耳酮）是一种天然产物，也是一种miR-34a(microRNA-34)的调节剂，以p53依赖性方式上调miR-34a表达，进而下调下游靶标Bcl-2、cyclin-D1、CDK6、SIRT1和FOXP1的表达，从而抑制肝细胞癌(HCC)的肿瘤生长和逆转前列腺癌中的化疗耐药性。

Pristimerin (Celastrol methyl ester) 是一种可逆的单酰基甘油脂肪酶高效抑制剂，IC50值为93 nM。

1-Methyladenine is a DNA alkylation product that undergoes damage reversal through oxidative demethylation for repair purposes.

Ciraparantag is an inhibitor of thrombin and factor Xa. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including unfractionated heparin, low-molecular-weight heparin, and certain direct oral anticoagulants.

Ciraparantag TFA is an inhibitor of thrombin and factor Xa. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including unfractionated heparin, low-molecular-weight heparin, and certain direct oral anticoagulants.

Ciraparantag acetate 是一种抗凝逆转剂，是一种小分子，专门设计用于通过电荷-电荷相互作用与普通肝素和低分子量肝素非共价结合。它显示出与直接口服抗凝剂 (DOAC) 相似的结合特性。

ABCB1-IN-2 (compound 16q) 作为一种功能性抑制剂，它能直接作用于ABCB1蛋白并稳定其结构，而不干扰ABCB1的表达和亚细胞性定位。此化合物能有效增强MCF-7 ADR细胞对紫杉醇（PTX）的反应，通过增加PTX的内部积累并抑制ABCB1介导的荧光素Rh123的积累与排出。因此，ABCB1-IN-2展现出其强大的逆转多药耐药（MDR）能力，具有作为MDR逆转剂的潜力。

DOCP (2-((2,3-Bis(oleoyloxy)propyl)dimethylammonio)ethyl hydrogen phosphate) 的结构表明，其电荷分布与传统的磷酸胆碱 (PC) 脂质正好相反。这种独特的构造由季胺位于双层界面和磷酸基团突出至水环境的布局构成。iPC 脂质因其反向电荷的特性，为研究双层表面电荷反转及其对生物物理性质和生物活性的影响提供了理想的平台。

Prenoverine是一种二苯甲醇衍生物，具有良好的多药耐药性逆转活性。

Acerinol is an active ingredient from traditional Chinese medicinal herbs. It could be used as a cancer multidrug resistance reversal agent. Acerinol can significantly stimulate the activity of ABCB1 ATPase without affecting the expression of ABCB1 on nei

trans-Trimethoxyresveratrol (MR-3) 是一种 Resveratrol(RSV) 的衍生物，与Resveratrol(RSV)相比，它可能是一个更有效的抗炎、抗血管新生的化合物。

Simetride is used in the Reversal of resistance to vincristine in P388 leukemia.

Deacetylforskolin is a diterpene and a derivative of forskolin that has been found inC. forskohliiand has diverse biological activities.1,2,3,4It activates rat adipocyte adenylyl cyclase (IC50= 20 μM) and inhibits glucose transport in rat adipocyte plasma membranes.2Deactylforskolin (30-1,000 μg kg) reduces blood pressure in spontaneously hypertensive rats.3It also attenuates hypercapnia-induced impairments in the passive avoidance response in mice.4 1.Gabetta, B., Zini, G., and Danieli, B.Minor Diterpenoids of Coleus forskohliiPhytochemistry28(3)859-862(1989) 2.Joost, H.G., Habberfield, A.D., Simpson, I.A., et al.Activation of adenylate cyclase and inhibition of glucose transport in rat adipocytes by forskolin analogues: structural determinants for distinct sites of actionMol. Pharmacol.33(4)449-453(1988) 3.Bhat, S.V., Dohadwalla, A.N., Bajwa, B.S., et al.The antihypertensive and positive inotropic diterpene forskolin: Effects of structural modifications on its activityJ. Med. Chem.26(4)486-492(1983) 4.McCulloch, A.J., Thomson, T.A., and Deacon, R.Hypoxic amnesia and its reversal with forskolinBiochem. Soc. Trans.17(1)212-213(1988)

Astragaloside II (Astrasieversianin VIII) 是一种分离自黄芪中的天然化合物。

Tectochrysin (Techtochrysine) 是Alpinia oxyphylla 的主要黄酮类化合物之一，能够抑制NF-κB 活性。

Cinobufotalin 是一种从蟾蜍的皮肤分泌物中提取的强心类固醇或丁二烯内酯。它已被用作强心药，利尿药和止血药，也是潜在的抗肺癌药物。

Sugammadex is an agent for reversal of neuromuscular blockade by the agent rocuronium in general anaesthesia. It is the first selective relaxant binding agent (SRBA). Sugammadex is a modified γ-cyclodextrin, with a lipophilic core and a hydrophilic periph

Coptisine (Coptisin) 是一种从黄连中分离到的生物碱，是非竞争性的IDO 抑制剂，Ki=为 5.8 μM，IC50=6.3 μM。

OY-101为口服生效的特异性P-glycoprotein(P-gp)抑制剂。该化合物可增强耐药性肿瘤的敏感性，并有效逆转多药耐药现象。相较于Tetrandrine，OY-101在水溶性、细胞毒性以及逆转活性方面均表现出改进。

P-gp inhibitor 3 是一种高效 P 糖蛋白（P-gp）抑制剂，通过激活 P-gp ATP酶抑制其外排功能，具有显著的多重耐药性（MDR）逆转能力，并能增强紫杉醇的抗肿瘤活性。

AcrB-IN-1 (Compound H6) 是一种有效的 AcrB 抑制剂。AcrB-IN-1 可用于逆转细菌多药耐药。

LL-37(17-32)为具有生物活性的肽段，为LL-37抗菌肽C末端结构域源自的活性片段。报道显示，LL-37(17-32)能逆转癌细胞系中ABCG2介导的多药耐药性。