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Anti-infection

Antibiotic Arenavirus Bacterial CMV Enterovirus Filovirus Fungal HBV HCV HCV Protease HIV HIV Integrase HIV Protease HSV Influenza Virus Orthopoxvirus Parasite TMV Reverse Transcriptase RSV SARS-CoV Virus Protease
Apoptosis

Apoptosis Bcl-2 Family Caspase c-Myc Ferroptosis FKBP IAP Family MDM-2/p53 PKD Necroptosis Pyroptosis RIP kinase Thymidylate Synthase TNF Receptor TRADD Cuproptosis
Autophagy

Autophagy FKBP LRRK2 Mitophagy OGA ULK
Cell Cycle/DNA Damage

Antifolate APC ATM/ATR Aurora Kinase BMI-1 Casein Kinase CDK Checkpoint Kinase (Chk) CRISPR/Cas9 Deubiquitinase DNA Alkylator/Crosslinker DNA/RNA Synthesis DNA-PK Early 2 Factor (E2F) Eukaryotic Initiation Factor (eIF) GAK G-quadruplex HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 DNA Stain Nucleoside Antimetabolite/Analog Nur77 p97 PAK PARP PERK Polo-like Kinase (PLK) PPAR RAD51 Cyclin G-associated Kinase (GAK) ROCK ATF6 Haspin Kinase Sirtuin SRPK PDI Telomerase TOPK Topoisomerase Wee1
Cytoskeletal Signaling

Arp2/3 Complex Dynamin Gap Junction Protein Integrin Kinesin Microtubule/Tubulin Mps1 Myosin PAK ROCK
Endocrinology/Hormones

Adrenergic Receptor Androgen Receptor Angiotensin-converting Enzyme (ACE) Aromatase Cholecystokinin Receptor TSH Receptor Estrogen Receptor/ERR GHSR Glucocorticoid Receptor GNRH Receptor Mineralocorticoid Receptor Opioid Receptor PGD synthase PGE synthase Progesterone Receptor Thyroid Hormone Receptor
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain HDAC Histone Acetyltransferase Histone Demethylase Histone Methyltransferase MicroRNA PARP PKC Protein Arginine Deiminase Methionine Adenosyltransferase (MAT) Sirtuin JAK
GPCR/G Protein

5-HT Receptor Adenosine Receptor Adenylate Cyclase (AC) Adiponectin Receptor Adrenergic Receptor Angiotensin Receptor Bombesin Receptor Bradykinin Receptor Cannabinoid Receptor CaSR CCR CGRP Receptor Cholecystokinin Receptor CRFR CXCR TSH Receptor Neuropeptide Y Receptor Dopamine Receptor EBI2/GPR183 Endothelin Receptor Formyl peptide receptor (FPR) GHSR Glucagon Receptor Glucocorticoid Receptor GNRH Receptor GPR109A GPR119 GPR139 GPR27 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR Melanocortin Receptor Melatonin Receptor mGluR Neurokinin Receptor Neurotensin Receptor Opioid Receptor Orexin Receptor (OX Receptor) Oxytocin Receptor P2Y Receptor PKG Prostaglandin Receptor Protease-Activated Receptor (PAR) Apelin Receptor (APJ) Ras GPR88 Free Fatty Acid Receptor E3 Ligase Ligand-Linker Conjugates RGS GPR4 Secretin Receptor Mas-related G-protein-coupled Receptor (MRGPR) GPR35 GPR52 MCHR1 (GPR24) Leukotriene Receptor GLP Receptor Somatostatin Receptor Arrestin Platelet-activating Factor Receptor (PAFR) Mas-related G-protein-coupled Receptor (MRGPR) Kisspeptin Receptor G Protein-coupled Receptor Kinase (GRK) G protein-coupled Bile Acid Receptor 1 Succinate Receptor 1 Protease Activated Receptor (PAR) Vasopressin Receptor

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HIV

HIV相关产品（150）

货号	产品名	中文名称	产品描述
SJ-BP0339	TAT TFA		TAT TFA (YGRKKRRQRRR) 源自人免疫缺陷病毒 (HIV-1) 的转录反式激活因子 (TAT)，是一种穿透细胞的肽。TAT 可以增加异源蛋白质的产量和溶解度。
SJ-MX3596	Lersivirine		Lersivirine is a non-nucleoside, next generation reverse transcriptase inhibitor (IC50 = 118 nM for the wild-type HIV-1 enzyme). It inhibits a panel of 14 single-point mutant HIV-1 reverse transcriptases with mean IC50 values within 10-fold of the wild-type enzyme. Lersivirine inhibits HIV-1 virus replication in MT-2 cells with EC50 values of 5.04, 13.1, and 34.9 nM at multiplicities of infection (MOIs) of 0.005, 0.05, and 0.5, respectively, and displays synergistic or additive effects when used in combination with a variety of antiretroviral agents.
SJ-MA0069D	Tenofovir hydrate	替诺福韦水合物	Tenofovir hydrate (GS 1278 hydrate) 是一种核苷酸逆转录酶 (nucleotide reverse transcriptase) 抑制剂，可用于 HIV和慢性乙型肝炎 (Hepatitis B; HBV) 的研究。
SJ-BP0213	DAPTA		DAPTA (RAP-101; DAPTA; DAPTA) 是一种合成肽，为 CCR5 抑制剂，同时具有抗 HIV 的活性。
SJ-MX2576	Dapivirine	达匹维林	Dapivirine (TMC120) 是二芳基嘧啶 (DAPY) 的原型，是具有口服活性的非核苷类逆转录酶抑制剂 (NRTI)。Dapivirine (TMC120) 可直接与 HIV 的逆转录酶结合。Dapivirine (TMC120)调节自噬并诱导 Akt、Bad 和 SAPK/JNK 的激活。
SJ-MA0076A	Raltegravir potassium	雷特格韦钾盐	Raltegravir potassium (formerly also known as MK-0518 potassium; trade name: Isentress) is a novel, potent integrase (IN) inhibitor for WT and S217Q PFV IN with IC50 of 90 nM and 40 nM in cell-free assays, respectively. Raltegravir is an antiretroviral drug used to treat HIV infection. Raltegravir binds to and inhibits integrase, an HIV enzyme that inserts viral genetic material into the genetic material of the infected human cell. Inhibition of integrase prevents insertion of HIV DNA into the human DNA genome, thus blocking HIV replication.
SJ-MA0069E	Tenofovir Disoproxil	替诺福韦酯	Tenofovir Disoproxil (Bis(POC)-PMPA) 是核苷酸逆转录酶抑制剂 (nucleotide reverse transcriptase inhibitor)，有潜力用于艾滋病和慢性乙型肝炎的研究。
SJ-MA0362	Temsavir		Temsavir (formerly known as BMS-626529) is a novel, potent attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells. Temsavir is also the phosphonooxymethyl prodrug of BMS-626529 that targets HIV-1 gp120 and prevents its binding to CD4(+) T cells. BMS-626529 had half-maximal effective concentration (EC(50)) values of6 log(10), with half-maximal effective concentration values in the low pM range against the most susceptible viruses.
SJ-MA0406	RN-18		RN-18是HIV-1病毒感染因子 ( HIV-1 Vif) 的拮抗剂，在非允许细胞 H9 中的 IC50 为6 µM。
SJ-MA0433	(S)-Tenofovir	(S)-替诺福韦	(S)-Tenofovir ((S)-GS 1278) 是 Tenofovir 的低活性 S 型异构体。Tenofovir 是一种核苷酸逆转录酶 (nucleotide reverse transcriptase) 抑制剂，可用于 HIV 和慢性乙型肝炎的研究 (Hepatitis B; HBV)。
SJ-MA0434	beta-L-D4A		beta-L-D4A is a nucleoside HIV-1 reverse transcriptase inhibitor.
SJ-MA0169	Inosine pranobex		Inosine pranobex (Imunovir; Delimmun; Groprinosin), a combinatinon of inosine, acetamidobenzoic acid, and dimethylaminoisopropanol, is a novel, potent, broad-spectrum antiviral agent potentially useful for HIV/AIDs infection. Inosine pranobex is also an immunopotentiator/immunostimulant, and has no direct effect on viral cells.
SJ-MA0280A	Erythromycin Ethylsuccinate	琥乙红霉素	Erythromycin Ethylsuccinate是一种抗生素，有用于多种细菌感染的潜能，具有与青霉素类似或稍宽于青霉素的抗菌谱。 Erythromycin Ethylsuccinate 具有抗 HIV-1 病毒的活性。
SJ-MA0352	Salicylanilide		Salicylanilide (also known as WR10019; 2-Hydroxybenzanilide) exhibits a wide range of biological activities including antiviral potency, antibacterial (including antimycobacterial) and antifungal activities. Some salicylanilides and salicylamides could inhibit HIV virus by targeting of HIV-1 integrase or reverse transcriptase. Hepatitis C virus could be potentially afflicted by salicylanilides on the level of two enzymes – NS3 protease and NS5B RNA polymerase.
SJ-MB0096	Ditiocarb sodium	二乙基二硫代氨基甲酸钠	Ditiocarb sodium (Sodium diethyldithiocarbamate) 是一种铜试剂，与 Cu2+ 溶液反应，生成络合物，提高了铜置换沉淀速率。Sodium diethyldithiocarbamate 可降低 HIV 感染。
SJ-MH0053	Megestrol acetate	醋酸甲地孕酮	Megestrol acetate (formerly BDH1298, SC10363; BDH-1298; SC-10363; Megace; Ovaban; Pallace; Maygace; Megestil; Niagestin) is a synthetic progestogen derivative that has been approved for use in the treatment of breast cancer and loss of appetite. Megestrol Acetate shows potent anti-proliferative activity in vitro against various cancer cell lines such as HepG2 cells with an IC50 value of 260 μM.
SJ-MA0063A	Nelfinavir		Nelfinavir is an antiretroviral drug used in the treatment of the human immunodeficiency virus (HIV).
SJ-MA0173A	Darunavir	达芦那韦	Darunavir is a potent human immunodeficiency virus type 1 (HIV-1) protease inhibitor with an IC50 value of 0.003 μM (HIV-1LAI). Moreover, Darunavir shows potent activity against multi-protease inhibitor-resistant HIV in vitro.
SJ-MA0443	Zalcitabine		Zalcitabine is a nucleoside analog reverse transcriptase inhibitor (NRTI).
SJ-MA0478	Saquinavir	沙奎那韦	Saquinavir is an HIV Protease Inhibitor used in antiretroviral therapy. Saquinavir inhibits both HIV-1 and HIV-2 proteases. Studies have also looked at Saquinavir as a possible anti-cancer agent.