59
11
2
5
6
Cat. No. | Product Name | ||
---|---|---|---|
L1700 | 抗病毒库 | 1040 compounds | |
1040 种具有抗病毒活性的化合物的特有集合,是筛选新型抗病毒药的有效工具;可用于高通量筛选和高内涵筛选; | |||
L1100 | 蛋白酶抑制剂库 | 343 compounds | |
343 种已知的小分子蛋白酶抑制剂的特有集合,可用于高通量筛选和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6255 |
Bromosporine
|
Epigenetic Reader Domain; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Bromosporine 是广谱 BRD2/4/9 和 CECR2 溴结构域抑制剂,IC50为0.41、0.29、0.122和0.017 μM。 | |||
T20062 |
Thiamine disulfide
二硫化硫胺,TDS,Daiomin,Algoneurina |
HIV Protease; Endogenous Metabolite | Metabolism; Microbiology/Virology; Proteases/Proteasome |
Thiamine disulfide (Algoneurina) 是一种存在于食物中的维生素,可作为膳食补充剂和药物生产。 它还充当许多中枢代谢酶的辅助因子。 | |||
T6098 |
Cabotegravir
GSK744,GSK-1265744,卡博特韦,S/GSK1265744 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Cabotegravir (S/GSK1265744) 是一种HIV 整合酶抑制剂,可研究艾滋病。它抑制OAT1 和OAT3,IC50值为 0.81 和0.41 μM。 | |||
T7212 |
Delavirdine mesylate
U 90152 (mesylate),BHAP-U 90152 (mesylate),Delavirdine (mesylate) |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Delavirdine mesylate (BHAP-U 90152(mesylate)) 是一种口服活性非核苷逆转录酶抑制剂。它抑制 HIV-1 病毒复制,可以用于艾滋病的相关研究。它选择性地抑制 HIV-1 逆转录酶,其选择性超过 DNA 聚合酶 α 和 DNA 聚合酶 δ 。 | |||
T1267 |
Abacavir
Epzicom,Ziagen,阿巴卡韦 |
Apoptosis; HIV Protease; Reverse Transcriptase | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Abacavir (Ziagen) 是一种核苷类似物逆转录酶抑制剂。 | |||
T70852 |
Atevirdine
U 85961 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Atevirdine 是一种 HIV-1 逆转录酶抑制剂,具有抗病毒活性,可用于研究艾滋病痴呆复合体(ADC)。 | |||
T3335 |
Darunavir Ethanolate
地瑞那韦乙醇盐,UIC 94017,Darunavir Ethanolate,TMC114,达芦那韦乙醇 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Darunavir Ethanolate (UIC 94017) 是一种HIV 蛋白酶抑制剂,可以用于 HIV/AIDS 的相关研究。对野生型 HIV-1 蛋白酶的Ki 值为1 nM。 | |||
T1595 |
Nevirapine
NSC 641530,奈韦拉平,BI-RG 587,奈伟拉平,NVP |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Nevirapine (NVP) 是一种 HIV-1逆转录酶非核苷抑制剂,Ki 值为 270 μM,可用于研究 HIV/AIDS。 | |||
T3632 |
Doravirine
多拉维林,多拉韦林,MK-1439 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Doravirine (MK-1439) 是一种高度特异性的HIV-1非核苷逆转录酶抑制剂,对野生型以及K103N 和Y181C 逆转录酶突变体的IC50值分别为 4.5 nM,5.5 nM 和 6.1 nM。 | |||
T7903 |
Saquinavir
Ro 31-8959,沙奎那韦 |
SARS-CoV; HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Saquinavir (Ro 31-8959) 是一种 HIV 蛋白酶抑制剂,可研究逆转录病毒。它也是 SARS-CoV 3CLpro 抑制剂,IC50为 1.36 μM。 | |||
T4697 |
ABBV-744
ABBV744 |
Epigenetic Reader Domain; HIV Protease | Chromatin/Epigenetic; Microbiology/Virology; Proteases/Proteasome |
ABBV-744 是一种 BDII 选择性 BET 溴结构域抑制剂,可抑制 BRD2/3/4。 它可研究炎症性疾病、癌症和艾滋病。 | |||
T24362 |
L 756423
L756423,MK-944a,MK944a,L-756,423,L-756423,MK 944a |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
L 756423 (L756423) 是一种新型有效且具有选择性和竞争性的HIV蛋白酶抑制剂,对 HIV-1 PR 的 Ki 值为0.049 nM。L 756423 能阻止HIV(IIIb)感染的 MT25 淋巴细胞在0.50-0.1nM处的扩散,可用于研究获得性免疫缺陷综合征(AIDS)。 | |||
T0688 |
Ganciclovir
BW 759,更昔洛韦,RS-21592,2'-Nor-2'-deoxyguanosine |
Nucleoside Antimetabolite/Analog; Others; Antibiotic; Antifection; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Ganciclovir (2'-Nor-2'-deoxyguanosine) 是核苷类似物和口服抗病毒药物,对CMV 具有抗病毒活性。它用于治疗与艾滋病相关的巨细胞病毒感染的并发症。 | |||
T0100 |
Atazanavir sulfate
阿扎那韦硫酸盐,BMS-232632,BMS-232632 sulfate,硫酸阿扎那韦 |
P450; SARS-CoV; HIV Protease; P-gp | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Atazanavir sulfate (BMS-232632 sulfate) 是一种氮杂肽和 HIV 蛋白酶抑制剂,与其他抗 HIV 药物联合用于治疗 HIV 感染和艾滋病。它也是SARS-CoV 3CLpro 抑制剂,IC50为 3.49 μM。 | |||
T6367 |
Abacavir sulfate
Abacavir Hemisulfate,硫酸阿巴卡韦,1592U89,ABC sulfate,Ziagen |
Apoptosis; HIV Protease; Reverse Transcriptase | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Abacavir sulfate (Ziagen) 是一种核苷类似物逆转录酶抑制剂,可用于 HIV 和 AIDS。 | |||
T2324 |
Darunavir
地瑞那韦,达芦那韦,TMC114 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Darunavir (TMC114) 是一种 HIV 蛋白酶抑制剂,用于治疗艾滋病和 HIV 感染。 由于单独使用时会出现抗病毒药物耐药性,因此与其他抗 HIV 药物联合使用。 | |||
T8736 |
Cidofovir dihydrate
HPMPC,(S)-HPMPC,GS 0504,西多福韦二水合物 |
Others | Others |
Cidofovir dihydrate (HPMPC) 是注射型巨细胞病毒 DNA 聚合酶抑制剂,通过选择性抑制病毒 DNA 聚合酶来抑制 CMV 复制,从而阻止病毒复制和转录。 | |||
T8826 |
3-AMINO-1,2,4-TRIAZINE
|
Others | Others |
3-AMINO-1,2,4-TRIAZINE 是一种芳香族生物活性化合物,已用于合成各种药物,包括抗真菌药物氟康唑、抗炎药物布洛芬和抗癌药物紫杉醇;也被用于设计新药,如抗艾滋病药物齐多夫定和抗疟疾药物青蒿素;以及用于合成各种其他化合物,如抗糖尿病药物二甲双胍和抗高血压药物赖诺普利。 | |||
T1525 |
Ritonavir
RTV,利托那韦,Abbott 84538,A 84538,ABT 538 |
Apoptosis; SARS-CoV; HIV Protease | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Ritonavir (ABT 538) 是一种 HIV 蛋白酶抑制剂,可研究 HIV 感染和 AIDS 。它也是 SARS-CoV 3CLpro 的抑制剂,IC50为 1.61 μM。 | |||
T0377 |
Clofazimine
NSC-141046,氯法齐明,氯苯吩嗪 |
DNA; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Clofazimine (NSC-141046) 是一种具有显著的抗炎效果的亚氨基酚嗪类染料,与其它抗分支杆菌药物联用来治疗AIDS 和克罗恩病。 | |||
T28306 |
PD 099560
PD099560,PD-099560 |
Others | Others |
PD 099560 is a non-peptide inhibitor of HIV-1 protease, a significant target enzyme in AIDS research. | |||
T71517 |
Nevirapine quinone methide
|
Others | Others |
Nevirapine quinone methide is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS. | |||
T70717 |
KNI 174
|
Others | Others |
KNI 174 is a new type of anti‐AIDS drug used as an HIV‐1 protease inhibitor | |||
T25535 |
Indinavir, threo-
Threo-indinavir,Indinavir sulfate specified impurity C |
Others | Others |
Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS. | |||
T68376 |
Indinavir lactone
|
Others | Others |
Indinavir lactone is a protease inhibitor used as a component of highly active antiretroviral therapy to treat HIV/AIDS. | |||
T5863L |
Indinavir
茚地那韦,MK-639,L 735 524,Crixivan |
Others | Others |
Indinavir (IDV) is an inhibitor of protease that is used as part of highly active antiretroviral therapy for the treatment of HIV/AIDS. | |||
T27171 |
Diethylhomospermine
DEHOP,BE-4-4-4,DEHSPM,DE-444 |
Others | Others |
Diethylhomospermine is a drug potentially for the treatment of AIDS-related chronic diarrhea.Diethylhomospermine also shows promising anticancer activity. | |||
T70147 |
Fipravirimat
|
Others | Others |
Fipravirimat 是一种有效的 HIV-1抑制剂。Fipravirimat 具有用于HIV 和 AIDS 研究的潜力。 | |||
TP2401 |
Peptide T amide
D-Ala(1)-peptide T amide |
||
Peptide T amide is an octapeptide segment of HIV envelope gp120 and is used in AIDS therapy. | |||
T69796 |
Nevirapine hemihydrate
|
Others | Others |
Nevirapine hemihydrate is a non-nucleoside reverse transcriptase inhibitor (NNRTI) studied for potential treatment of HIV-1 infection and AIDS. | |||
T74106 |
Hydroxy ritonavir
|
Others | Others |
Hydroxy ritonavir 是 Ritonavir 的代谢物。Ritonavir 是用于研究HIV 感染和 AIDS 的HIV 蛋白酶的抑制剂。 | |||
T63602 |
ddCTP trisodium
|
Others | Others |
ddCTP trisodium 是一种核苷类似物,靶向人类免疫缺陷病毒 (HIV) 的逆转录酶,可用于研究艾滋病 (AIDS)。ddCTP trisodium 是一类双脱氧核糖核苷酸 (ddNTPs),也是一种 DNA 聚合酶链延长抑制剂,能够用于 DNA 测序的研究。 | |||
T62690 |
HIV-1 inhibitor-46
|
Others | Others |
HIV-1 inhibitor-46 (compound 13d) 是一种 HIV-1 非核苷类逆转录酶的有效抑制剂 (EC50: 1.425 μM)。HIV-1 inhibitor-46 能够用于研究艾滋病 (AIDS)。 | |||
T62070 |
HIV-1 inhibitor-31
|
Others | Others |
HIV-1 inhibitor-31 (compound 4) 是一种 HIV-1 的有效抑制剂。HIV-1 inhibitor-31 能够用于研究艾滋病。 | |||
T72568 |
HIV-1 inhibitor-53
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
HIV-1inhibitor-53 是一种抑制HIV-1蛋白酶(PR)与逆转录酶(RT)的双重抑制剂,其IC50值分别为1.93 nM与2.35 μM,用于获得性免疫缺陷综合征(AIDS)相关的研究。 | |||
T71518 |
Zidovudine diphosphate
|
Others | Others |
Zidovudine diphosphate is an antiretroviral medication used to prevent and treat HIV/AIDS. It is of the nucleoside analog reverse-transcriptase inhibitor (NRTI) class. Zidovudine inhibits the enzyme (reverse transcriptase) that HIV uses to synthesize DNA, thus preventing viral DNA from forming. | |||
T71983 |
Zidovudine glucuronide
|
Others | Others |
Zidovudine glucuronide is an antiretroviral medication used to prevent and treat HIV/AIDS. It is of the nucleoside analog reverse-transcriptase inhibitor (NRTI) class. Zidovudine inhibits the enzyme (reverse transcriptase) that HIV uses to synthesize DNA, thus preventing viral DNA from forming. | |||
T39068 |
Fomivirsen sodium
|
Others | Others |
Fomivirsen sodium is an antisense 21 mer phosphorothioate oligonucleotide. Fomivirsen is an antiviral agent that is used cytomegalovirus retinitis (CMV) research, incluiding in AIDs. Fomivirsen sodium binds to and degrades the mRNAs encoding CMV immediate-early 2 protein (required for viral replication), thus providing bioactive effects for CMV retinitis by inhibition of virus proliferation. | |||
T71066 |
Cidofovir sodium
|
Others | Others |
Cidofovir sodium is the salt form of Cidofovir, a Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor that is an injectable antiviral medication primarily used as a treatment for cytomegalovirus (CMV) retinitis in people with AIDS. The mechanism of action of cidofovir is as a DNA Polymerase Inhibitor. The chemical classification of cidofovir anhydrous is Nucleoside Analog. | |||
T74939 |
HIV protease-IN-1
|
Others | Others |
HIVprotease-IN-1 (compound 1·succinate) 是一种有效的HIV 蛋白酶 (HIV protease) 非肽抑制剂,可用于艾滋病的研究。 | |||
T19228 |
Calcitriol Impurities D
24-Homo Calcitriol,24-Homo-1,25-dihydroxyvitamin D3 |
Antiviral | Immunology/Inflammation |
Calcitriol Impurities D (24-Homo Calcitriol) 是维生素的一种激素形式,可促进HL-60人早幼粒细胞白血病细胞分化为单核细胞。Calcitriol Impurities D 具有骨吸收活性,抑制人类免疫缺陷病毒在人体细胞中的复制。Calcitriol Impurities D 具有抗病毒活性们可以用于治疗艾滋病和病毒感染。 | |||
T63306 |
HIV-1 inhibitor-32
|
Others | Others |
HIV-1 inhibitor-32 是 HIV-1 的有效抑制剂,能够作用于野生型 HIV (IC50: 34 nM),能够用于研究艾滋病。 | |||
T84453 |
1-Palmitoyl-2-Lauroyl-sn-glycero-3-PC
1-Palmitoyl-2-Lauroyl-sn-glycero-3-Phosphatidylcholine |
Others | Others |
1-Palmitoyl-2-lauroyl-sn-glycero-3-PC (1,2-PLPC) is a phospholipid with palmitoyl (16:0) and lauryl (12:0) acyl chains at the sn-1 and sn-2 positions, respectively. This mixed-chain phosphatidylcholine aids in researching the role of chain-chain contact interactions in maintaining the structural stability of lipid membrane bilayers. | |||
T83488 |
[Lys8] Vasopressin Desglycinamide
|
||
"[Lys8] Vasopressin Desglycinamide,一种抗利尿激素类似物,主要应用于促进主动及被动回避行为的维持。该化合物有助于记忆巩固过程。" | |||
T64303 |
ZLM-66
|
Others | Others |
ZLM-66 是一种多拉维林 (Doravirine) 类似物,也是一种 non-nucleoside reverse transcriptase (NNRTIs) 的有效抑制剂,能够作用于野生型 HIV-1 逆转录酶 (IC50: 41 nM)、野生型 HIV-1 (EC50: 13 nM)。ZLM-66 能够用于研究艾滋病 (AIDS)。 | |||
T62782 |
HIV-1 inhibitor-34
|
Others | Others |
HIV-1 inhibitor-34 (compound 5q) 是一种有效的、选择性的 HIV-1 抑制剂,作用于 HIV-1 (EC50: 6.4 nM)、MT-4 细胞 (CC50: 16 μM)。HIV-1 inhibitor-34 能够用于研究艾滋病。 | |||
T75232 |
2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine
|
Others | Others |
2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine 是一种具有抗癫痫潜能的尿嘧啶核苷类似物。其不仅用于研究抗惊厥和抗焦虑活性,也用于开发新型降压药物。 | |||
T75112 |
LSN3160440
|
Others | Others |
LSN3160440 是GLP-1R 的变构调节剂,可作为蛋白-蛋白相互作用(PPI)的稳定剂或分子胶,协助无活性GLP-1 (9-36) NH2粘附在GLP-1R 上。 | |||
T62353 |
HIV-1 inhibitor-33
|
Others | Others |
HIV-1 inhibitor-33 (compound 5n) 是一种有效的、选择性的 HIV-1 抑制剂,作用于 HIV-1 (EC50: 8.6 nM)、MT-4 细胞 (CC50: 18 μM)。HIV-1 inhibitor-33 能够用于研究艾滋病。 | |||
T80963 |
TPEQM-DMA
|
||
TPEQM-DMA为近红外二区光敏剂,能在癌性线粒体中积累,抑制癌细胞生长。其显著I型光疗效果,有助于克服光动力疗法(PDT)治疗低氧肿瘤的限制。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5748 |
Ipecoside
AIDS031406 |
Others | Others |
Ipecoside (AIDS031406) 是一种生物碱,分离自Psychotria。 | |||
T1284 |
Megestrol acetate
SC10363,醋酸甲地孕酮,BDH1298 |
Glucocorticoid Receptor; Estrogen/progestogen Receptor; Progesterone Receptor; HIV Protease; Autophagy | Autophagy; Endocrinology/Hormones; Microbiology/Virology; Others; Proteases/Proteasome |
Megestrol acetate (BDH1298) 是具有口服活性的合成孕激素。它还具有抗雄激素特性,可用于治疗厌食症和恶病质。 | |||
T1388 |
Fluconazole
氟康唑,UK-49858 |
Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Fluconazole (UK-49858) 是一种对多种真菌具有活性的三唑类抗真菌剂,抑制 C. albicans 和 Candida kefyr 的 IC99为 0.20 μg/mL 至 0.39 μg/mL。 | |||
T74293 |
Allolithocholic acid
|
Others | Others |
Allolithocholic acid 是一种类固醇酸,在正常血清和粪便中可发现。该化合物促进脂肪与甾醇在肠道及肝脏的排泄、吸收与运输。 | |||
T2598 |
Thymopentin
TP5,胸腺五肽 |
Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Thymopentin (TP5) 是主要由胸腺皮质和髓质上皮细胞分泌的生物特性肽。它能促使自人类胚胎干细胞产生 T 细胞群。它是有效免疫调节剂,具有很短的血浆半衰期(30 秒)。 | |||
T2O2733 |
L-Cystine
Cystine Acid,cystine,胱氨酸,L-胱氨酸 |
Antioxidant; Ferroptosis; Endogenous Metabolite | Apoptosis; Metabolism; oxidation-reduction |
L-Cystine (Cystine Acid) 是一种从半胱氨酸氨基酸硫醇侧链氧化获得的含硫衍生物。它起到抗氧化剂的作用,保护组织免受辐射和污染,减缓衰老过程。它还有助于蛋白质合成。 | |||
T4S0797 |
Berberine
小檗碱,Berberin,Umbellatine,黄连素 |
Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Berberine (Umbellatine) 属于生物碱类天然产物,可以激活 AMPK、抑制 DNA 拓扑异构酶、诱导 ROS 生成。Berberine 具有抗肿瘤、抗菌、降血糖、降血脂等生物学活性。 | |||
TN2115 |
Pseudohypericin
|
Others; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Others |
Pseudohypericin has photocytotoxic, and antiretroviral activities, it has potential therapeutic value in diseases such as AIDS. | |||
TN7260 |
Z3-Dodecenyl E2-butenoate
|
Others | Others |
Z3-Dodecenyl E2-butenoate, a female sex pheromone of the sweet potato weevil (C. formicarius), is utilized for baiting and trapping male sweet potato weevils. This method aids in managing their populations in agricultural fields while minimizing insecticide use. | |||
T3S0804 |
Worenine
甲基黄连碱,Worenin |
Others | Others |
Worenine (Worenin) 是一种从黄连中提取的物质。它在大鼠体内第一阶段代谢中显示出脱氢,氢化,羟基化和脱亚甲基反应。在大鼠体内 II 期代谢中显示为硫酸化和葡萄糖醛酸化反应。 | |||
TN4585 |
Moronic acid
|
HIV Protease; Antifection; HSV | Microbiology/Virology; Proteases/Proteasome |
Moronic acid shows oral therapeutic efficacy in HSV-infected mice and possessed novel anti-HSV activity. It also shows significant anti-HIV activity (EC(50) 186) and was modified to develop more potent anti-AIDS agents. Moronic acid is a new structural lead for anti-EBV drug development, can substantially reduce the numbers of EBV particles produced by the cells after lytic induction. Morolic and moronic acids have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an... |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-01467 |
Oncostatin M/OSM Protein, Human, Recombinant (E. coli, His)
Oncostatin-M,OSM |
Human | E. coli |
Oncostatin M (OSM) is a glycoprotein belonging to the interleukin-6 family of cytokines that includes leukemia-inhibitory factor, granulocyte colony-stimulating factor, and interleukin 6. OSM encodes a growth regulator, which Inhibits the proliferation of a number of tumor cell lines. It stimulates proliferation of AIDS-KS cells. OSM regulates cytokine production, including IL-6, G-CSF and GM-CSF from endothelial cells. OSM is considered as a pleiotropic cytokine that initiates its biological ac... | |||
TMPH-01509 |
SPAM1 Protein, Human, Recombinant (His)
Sperm adhesion molecule 1,Hyaluronidase PH-20,Sperm surface ... |
Human | E. coli |
Involved in sperm-egg adhesion. Upon fertilization sperm must first penetrate a layer of cumulus cells that surrounds the egg before reaching the zona pellucida. The cumulus cells are embedded in a matrix containing hyaluronic acid which is formed prior to ovulation. This protein aids in penetrating the layer of cumulus cells by digesting hyaluronic acid. | |||
TMPJ-01337 |
IL-21R Protein, Mouse, Recombinant (aa 20-236, His)
Nilr,IL-21R,Interleukin-21 receptor,IL-21 receptor,Il21r |
Mouse | HEK293 Cells |
Interleukin-21 receptor (IL-21R) is a type I transmembrane glycoprotein within the class I cytokine receptor family, type 4 subfamily. IL-21R is expressed mainly on B cells, NK cells, and activated T cells, but is also found on dendritic cells, alternatively activated macrophages, intestinal lamina propria fibroblasts and epithelial cells, and keratinocytes. Both IL-21 and IL-4 are necessary for efficient B cell IgG1 production and normal germinal center architecture. B cell IL-21 R engagement i... | |||
TMPY-02518 |
TCL1A Protein, Human, Recombinant (His)
TCL1,T-cell leukemia/lymphoma 1A |
Human | E. coli |
T-cell leukemia/lymphoma protein 1A (abbreviated for TCL1A) is a member of the TCL1 family. TCL1 protooncogene is expressed in CD3-CD4-CD8-precursor T cells and is extinguished at the CD4+CD8+stage of thymocyte development. In B cells, TCL1 is first expressed in pro-B cells and remains high in naive mantle zone B cells of peripheral lymphoid tissues. The TCL1 protooncogene is overexpressed in many mature B cell lymphomas, especially from AIDS patients. It has been demonstrated that TCL1 is a pow... | |||
TMPJ-00920 |
CD40 Ligand Protein, Mouse, Recombinant (aa 112-260, His)
TNFSF5,Tumor necrosis factor ligand superfamily member 5,CD4... |
Mouse | HEK293 Cells |
CD40 Ligand, also known as TNFSF5, CD154, is a type II transmembrane glycoprotein member of the TNF superfamily. Mature mouse CD40 Ligand consists of a 22 amino acid (aa) cytoplasmic domain, a transmembrane segment, and a 214 aa extracellular region. CD40 Ligand is expressed as a homotrimer on platelets and activated T cells and B cells. It is upregulated following stimulation of basophils, eosinophils, fibroblasts, mast cells, monocytes, natural killer cells, vascular endothelial cells, and sm... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMID-0205 |
Nevirapine-d4
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Nevirapine-d4 是 Nevirapine 的氘代化合物。Nevirapine 的 CAS 号为 129618-40-2。Nevirapine 是一种HIV-1逆转录酶非核苷抑制剂,Ki值为 270 μM,可用于研究 HIV/AIDS。 | |||
TMID-0206 |
Nevirapine-d3
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Nevirapine-d3 是 Nevirapine 的氘代化合物。Nevirapine 的 CAS 号为 129618-40-2。Nevirapine 是一种HIV-1逆转录酶非核苷抑制剂,Ki值为 270 μM,可用于研究 HIV/AIDS。 | |||
TMID-0081 |
Fluconazole-d4
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Fluconazole-d4 是 Fluconazole 的氘代化合物。Fluconazole 的 CAS 号为 86386-73-4。Fluconazole是一种对多种真菌具有活性的三唑类抗真菌剂,抑制C. albicans和Candida kefyr的 IC99为 0.20 μg/mL 至 0.39 μg/mL。 | |||
TMIJ-0217 |
Abacavir-d4
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Abacavir-d4 是 Abacavir 的氘代化合物。Abacavir 的 CAS 号为 136470-78-5。Abacavir是一种核苷类似物逆转录酶抑制剂。 | |||
TMIJ-0306 |
Ganciclovir-d5
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Ganciclovir-d5 是 Ganciclovir 的氘代化合物。Ganciclovir 的 CAS 号为 82410-32-0。Ganciclovir是核苷类似物和口服抗病毒药物,对CMV具有抗病毒活性。它用于治疗与艾滋病相关的巨细胞病毒感染的并发症。 | |||
TMIJ-0076 |
Ritonavir-13C-d3
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Ritonavir-13C-d3 是 Ritonavir 的 13C 和氘代化合物。Ritonavir 的 CAS 号为 155213-67-5。Ritonavir 是一种 HIV 蛋白酶抑制剂,可研究 HIV 感染和 AIDS 。它也是SARS-CoV 3CLpro的抑制剂,IC50为 1.61 μM。 |