125
23
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2331 |
Solithromycin
索利霉素,OP-1068,CEM-101 |
Antibacterial; Antibiotic | Microbiology/Virology |
Solithromycin (OP-1068) 是口服可生物利用的抗菌剂,抑制肺炎链球菌、葡萄球菌、金黄色葡萄球菌和流感嗜血杆菌的细胞活力、蛋白质合成和生长速率, IC50 值分别为 7.5 ng/mL、40 ng/mL 和 125 ng/mL。它可与核糖体的大 50S 亚基结合抑制蛋白质生物合成。 | |||
T39810 | CEM114 | ||
CEM114 is a potent chemical compound known as a chemical epigenetic modifier (CEM). It functions by employing CRISPR-Cas9 systems to harness endogenous chromatin machinery, thereby exerting its epigenetic modifying effects. | |||
T9104 |
TJ191
|
Apoptosis | Apoptosis |
TJ191 是一种选择性抗癌试剂,靶向低 TβRIII 表达的恶性T 细胞白血病/淋巴瘤细胞,可研究癌症。 | |||
T20038 |
2-Fluoroadenine
NSC-27364,NSC 27364,NSC27364,2-氟腺嘌呤 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2-Fluoroadenine (NSC-27364) 对非增殖性和增殖性肿瘤细胞具有毒性。2-Fluoroadenine 可用于抗癌症的相关研究。 | |||
T6018 |
Zosuquidar trihydrochloride
唑喹达三盐酸盐,Zosuquidar (LY335979) 3HCl,RS 33295-198 trihydrochloride,RS 33295-198 (D06387) 3HCl,Zosuquidar 3HCl,LY-335979 trihydrochloride |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种P-糖蛋白抑制剂,Ki 值为 59 nM。 | |||
T0370 |
Pheniramine maleate
Daneral,Inhiston,Trimetose,马来酸非尼拉敏 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物,可与组胺 H1 受体结合,从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。 | |||
T5858 |
Sertindole
Lu 23-174,舍吲哚 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Sertindole (Lu 23-174) 是一种非典型抗精神病药,可与多巴胺 D2 受体和血清素受体亚型 5-HT1D、5-HT2A 和 5-HT2C 结合,Kd 值分别为 2.7、20、0.14 和 6 nM。 | |||
T9005 |
VPC-80051 racemate
|
Others | Others |
VPC-80051 是一种有效的 hnRNP A1 剪接活性抑制剂,靶向 hnRNP A1 RBD 并降低 22Rv1 CRPC 细胞系中的 AR-V7 信使水平。 | |||
T12400 |
Peliglitazar racemate
(Rac)-Peliglitazar,(Rac)-BMS 426707-01,BMS 426707-01 racemate |
PPAR | DNA Damage/DNA Repair; Metabolism |
Peliglitazar racemate(BMS 426707-01 racemate) 是 Peliglitazar 的外消旋体。Peliglitazar racemate 可作为潜在的抗糖尿病和抗肥胖剂。 | |||
T61477 |
dCeMM2
|
Molecular Glues | PROTAC |
dCeMM2 (Compound 2) 是一种胶降解剂。dCeMM2 促使 CDK12-cyclin K 与 CRL4B 连接酶复合物的相互作用,导致 cyclin K 的泛素化及降解。 | |||
T22988 |
MK-4827 Racemate
Niraparib Racemate,2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MK-4827 Racemate (Niraparib Racemate) 是一种选择性 PARP1 和 PARP2 抑制剂,IC50 分别为 3.8 nM 和 2.1 nM,对 PARP3、V-PARP 和 Tank1 的选择性超过 330 倍。 | |||
T16731 |
Rentiapril racemate
(Rac)-SA-446,SA-446 racemate,(Rac)-Rentiapril |
Angiotensin-converting Enzyme (ACE) | Metabolism |
Rentiapril racemate (SA-446 racemate) 是 Rentiapril 的外消旋体。Rentiapril racemate 具有抗炎活性,可用于研究青光眼。 | |||
T76750 |
Cemiplimab
REGN-2810,SAR-439684 |
Others | Others |
Cemiplimab (Anti-Human PD-1) 是一种针对程序性细胞死亡受体 1 (PD-1) 的人单克隆抗体,也是一种检查点抑制剂,可阻断 PD-1/PD-L1 介导的 T 细胞抑制,可用于转移性癌症和鳞状细胞皮肤癌研究。 | |||
T3562 |
Valrocemide
TV1901,N-丙戊酰基甘氨酰胺,N-Valproylglycinamide,丙戊塞胺 |
Others | Others |
Valrocemide (TV1901) 是有前景的抗癫痫候选药物,具有广泛的抗惊厥特性。 | |||
T22253 |
AG-120 (racemic)
1-(4-氰基-2-吡啶基)-5-氧代-L-脯氨酰-2-(2-氯苯基)-N-(3,3-二氟环丁基)-N2-(5-氟-3-吡啶基)甘氨酰胺 |
Dehydrogenase | Metabolism |
AG-120 (racemic) 是 AG-120 的外消旋混合物,是一种可口服的异柠檬酸脱氢酶 1 型 (IDH1) 抑制剂,具有潜在的抗肿瘤活性。 | |||
T11178L |
ELN318463 racemate
ELN318463 (racemate),ELN 318463 racemate |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
ELN318463 racemate (ELN 318463 racemate) 是 ELN318463 的外消旋体,ELN318463 是一种淀粉样前体蛋白 (APP) 选择性 γ-分泌酶抑制剂。 | |||
T70407 |
cemadotin free base
LU103793 free base |
Microtubule Associated | Cytoskeletal Signaling |
Cemadotin free base(LU103793 free base) 是一种新型的抗限定性肽 ,是一种新型的抗有丝分裂肽 ,是Dolastatin 15的类似物 。Dolastatin 15是一种天然存在的细胞毒肽,可阻断有丝分裂并抑制微管(管蛋白),Ki 为1μM。Cemadotin 用于研究抗癌。 | |||
T50055 |
Milacemide
|
MAO | Metabolism; Neuroscience |
Milacemide 是一种甘氨酸前药和 MAO-B 抑制剂。已经研究了米拉塞米对人类记忆的影响以及作为阿尔茨海默病症状的潜在治疗方法。 | |||
T3120 |
K858 (Racemic)
K858 Racemic,K858 |
Apoptosis; Kinesin | Apoptosis; Cytoskeletal Signaling |
K858 Racemic (K858) 是一种选择性有丝分裂驱动蛋白 Eg5 抑制剂,以 ATP 非竞争性方式起作用,IC50值为 1.3 μM。 | |||
T20700 |
Racemetirosine
|
Others | Others |
Racemetirosine 是一种酪氨酸 3-单加氧酶抑制剂,因此会抑制儿茶酚胺的合成。 | |||
T6801 |
CeMMEC13
|
Carboxypeptidase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Proteases/Proteasome |
CeMMEC13 是一种异喹啉酮,可选择性抑制 TAF1 的第二个溴结构域,IC50为 2.1 μM。 | |||
T14864 |
Caracemide
NSC-253272,卡醋胺 |
Others; DNA/RNA Synthesis; Antibacterial | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Caracemide (NSC-253272) 抑制大肠杆菌的核糖核苷酸还原酶。 Caracemide 可用于抗癌研究。 | |||
T6809 |
CPI-169 racemate
CPI 169,CPI-169,CPI169 |
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
CPI-169 racemate (CPI 169) 是CPI-169的消旋体。CPI-169 是一种有效的选择性 EZH2 抑制剂,对 EZH2 WT、EZH2 Y641N 和 EZH1 的 IC50 分别为 0.24、0.51 和 6.1 nM。 | |||
T4345 |
CeMMEC1
CeMMEC1 HCl |
Epigenetic Reader Domain; Carboxypeptidase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome |
CeMMEC1 是一种 BRD4 抑制剂,对 TAF1 有很好的亲和力,IC50为0.9 μM。 | |||
T6425 |
BTZ043 Racemate
BTZ044,BTZ10526038,Benzothiazinone 10526038 |
Antibacterial; DprE1 | Microbiology/Virology; Others |
BTZ043 Racemate (Benzothiazinone 10526038) 是一种癸二烯基磷酰-β-D-核糖 2'-差向异构酶(DprE1) 抑制剂,用作新的抗分枝杆菌剂。 | |||
T12215 |
Nexopamil racemate
(Rac)-Nexopamil |
Calcium Channel; 5-HT Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Nexopamil racemate((Rac)-Nexopamil) 是 Nexopamil 的外消旋体。Nexopamil racemate 具有潜在的抗哮喘和抗溃疡活性。 | |||
T67778 |
dCeMM1
|
Molecular Glues | PROTAC |
dCeMM1 是 RBM39 分子胶降解剂,可以降低 WT KBM7 细胞中 RBM39 水平的表达。dCeMM1 活性发挥通过重定向 CRL4DCAF15 连接酶进行。 | |||
T10464L |
Atuveciclib Racemate
BAY-1143572 Racemate,阿维西利 |
CDK | Cell Cycle/Checkpoint |
Atuveciclib Racemate (BAY-1143572 Racemate) 是 Atuveciclib 的外消旋混合物。 Atuveciclib 是口服有效的 P-TEFb/CDK9高选择性抑制剂,CDK9/CycT1的 IC50为13 nM。 | |||
T10591 |
BPO-27 racemate
BPO-27 (racemate) |
CFTR; Autophagy | Autophagy; Membrane transporter/Ion channel |
BPO-27 racemate (BPO-27(racemate)) 是一种CFTR 抑制剂,IC50为8 nM。 | |||
T2344L |
LY 344864 racemate
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
LY 344864 racemate 是一种 5-HT1F 受体激动剂。 | |||
T3534 |
Tetrabenazine Racemate
Nitoman,丁苯那嗪外消旋体,丁苯那嗪,Ro 1-9569 Racemate,Rubigen,TETRABENAZINE |
Monoamine Transporter | Membrane transporter/Ion channel |
Tetrabenazine Racemate (Rubigen) 是一种选择性和可逆的囊泡单胺转运蛋白 2(VMAT-2) 抑制剂。它阻断神经递质吸收到肾上腺素能储存囊泡中,并已被用作囊泡运输系统的高亲和力标记。 | |||
T7359 |
CAY10471 Racemate
TM30089 Racemate,3-[[(4-氟苯基)磺酰基]甲基氨基]-1,2,3,4-四氢-9H-咔唑-9-乙酸 |
GPR; Prostaglandin Receptor | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation |
CAY10471 Racemate (TM30089 Racemate) 是一种高选择性的 CRTH2/DP 2 受体拮抗剂,对 hCRTH2 的Ki 值为 0.6 nM,对其选择性远高于人血栓素 A2 受体 TP 或 PGD2 受体 DP。它对大小鼠的同源 CRTH2 也具有拮抗作用。 | |||
T3449 |
Bay 41-4109 racemate
|
HBV | Microbiology/Virology |
BAY 41-4109 racemate 是BAY 41-4109的消旋体。BAY 41-4109有效抑制人乙型肝炎病毒,IC50值为53 nM。 | |||
T7504 |
Necrostatin 2 racemate
5-[(7-氯-1H-吲哚-3-基)甲基]-3-甲基-2,4-咪唑烷二酮,Necrostatin-2 racemate |
RIP kinase | Apoptosis; NF-κB |
Necrostatin 2 racemate (Necrostatin-2 racemate) 是一种特异性的RIPK1抑制剂,是一种稳定型 Nec-1。 | |||
T9758 |
dCeMM3
2-(1H-benzimidazol-2-ylsulfanyl)-N-(5-chloropyridin-2-yl)acetamide |
Others | Others |
dCeMM3 (2-(1H-benzimidazol-2-ylsulfanyl)-N-(5-chloropyridin-2-yl)acetamide) 是一种胶降解剂,可以诱导 cyclin K 的泛素化和降解。机制是通过促进 CDK12-cyclin K 与 CRL4B 连接酶复合物的相互作用。 | |||
T27143 |
Delucemine Hydrochloride
NPS 1506,Delucemine,Delucemine HCl,NPS1506,NPS-1506 |
NMDAR | Neuroscience |
Delucemine Hydrochloride (Delucemine) 是一种多胺NMDA受体拮抗剂,可用于研究抑郁症和阿尔茨海默症等神经系统疾病。 | |||
T1467 |
Acemetacin
阿西美辛,K-708,TVX 1322 |
COX | Immunology/Inflammation; Neuroscience |
Acemetacin (TVX 1322) 是一种非甾体抗炎类的化合物。 | |||
T60471 | Lanicemine dihydrochloride | ||
Lanicemine (AZD6765) dihydrochloride 是NMDA 通道的低捕获拮抗剂,Ki 值为 0.56-2.1 μM,在CHO 和爪蟾卵母细胞的IC50分别为 4-7 μM 和 6.4 μM。Lanicemine (AZD6765) dihydrochloride 具有持续的抗抑郁功效。 | |||
T10481 | BAY 73-6691 racemate | Others | Others |
BAY 73-6691 racemate is a phosphodiesterase 9 inhibitor. | |||
T11859 |
Litronesib Racemate
LY-2523355 Racemate,KF-89617 Racemate |
Others | Others |
Litronesib is a selective, allosteric inhibitor of kinesin Eg5.Litronesib (Racemate) is the racemate of litronesib. | |||
T13081 |
Taranabant racemate
MK-0364 racemate |
Cannabinoid Receptor | GPCR/G Protein |
Taranabant racemate is an antagonist and/or inverse agonist of the Cannabinoid-1 (CB1) receptor. | |||
T16440 |
Ibrutinib Racemate
PCI-32765 (Racemate) |
Others | Others |
Ibrutinib is a selective, irreversible Btk inhibitor (IC50: 0.5 nM). Ibrutinib Racemate is the racemate of Ibrutinib. | |||
T15829 | L 888607 Racemate | Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
L 888607 Racemate is a selective antagonist of prostaglandin D2 receptor subtype 1 (DP1) (Kis: 132 nM and 17 nM for DP1 and thromboxane A2 receptor (TP), respectively). | |||
T13700 |
GDC-0927 Racemate
SRN-927 Racemate |
Others | Others |
GDC-0927 Racemate is a degrader of estrogen receptor, is used in the research of ER-related diseases, potently inhibits ER-α activity, with an IC50 of 0.2 nM. | |||
T23949 |
Dacemazine hydrochloride
Ahistan HCl,Dacemazine HCl,Histantine HCl,UNII-DK78VKA001 |
||
Dacemazine is a phenothiazine derivative that acts as a histamine antagonist at the H1 subtype. It was also assessed as a possible anticancer drug. | |||
T72753 |
RSV604 racemate
A-60444 racemate |
||
RSV604 (A-60444) racemate 是一种外消旋混合物,与 S-异构体相比,RSV604 racemate 对呼吸道合胞病毒(RSV)菌株的作用效果弱很多。 | |||
T13293 |
Veledimex racemate
RG-115932 racemate,INXN-1001 racemate |
Others | Others |
Veledimex racemate, the racemic form of veledimex, is an orally available, small-molecule ligand that activates the RheoSwitch Therapeutic System. | |||
T13814 |
Pemafibrate (racemate)
K13675 (racemate) |
Others | Others |
Pemafibrate racemate is the racemate of pemafibrate | |||
T62670 |
Cemdomespib
|
||
Cemdomespib (KU-596) 是一种高效的二代 Hsp90 调节剂。Cemdomespib 能够诱导热休克反应,诱导 Hsp70 水平,具有神经保护作用。Cemdomespib 具有改善糖尿病周围神经病变模型感觉缺陷的疗效。 | |||
T12351 |
p53 and MDM2 proteins-interaction-inhibitor (racemic)
p53-and-mdm2-proteins-interaction-inhibitor-racemic |
Others | Others |
p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7220 |
Prohydrojasmon racemate
Propyl dihydrojasmonate,茉莉酮,Prohydrojasmon |
Others | Others |
Prohydrojasmon racemate (Propyl dihydrojasmonate) 是 Prohydrojasmon 的外消旋体。其中Prohydrojasmon 是合成的植物生长调节剂。 | |||
T2S1682 |
Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside
Pinocembrin 7-O-(3''-galloyl-4'',6''-(S)-hexahydroxydiphenoyl)-beta-D-glucose,pinocembrin-7-o-3-o-galloyl-4-6-hexahydroxydiphenoyl-beta-d-glucoside |
Amylase | Metabolism |
Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside 可抑制 α-淀粉酶活性,IC50值为0.03 umol/ml。 | |||
T2992 |
Pinocembrin
乔松素,5,7-Dihydroxyflavanone,Dihydrochrysin,Galangin flavanone,松属素 |
NF-κB; Reactive Oxygen Species; Antibacterial; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Pinocembrin (5,7-Dihydroxyflavanone) 是从蜂胶中得到的黄酮类物质,是一种竞争性组氨酸脱羧酶抑制剂,也是抗过敏剂,具有抗氧化、抗菌、抗炎的作用。 | |||
TN2078 |
Pinocembrin chalcone
2',4',6'-Trihydroxychalcone,Pinocembrinchalcone |
Calcium Channel; Tyrosinase; Antibacterial; Antifection | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Proteases/Proteasome |
Pinocembrin chalcone 是一种具有抗诱变作用的酪氨酸酶抑制剂。 Pinocembrin 查尔酮可用于预防胃溃疡的研究。 | |||
T19720 |
Colcemid
C 12669,C-12669,NSC-3096,Kolchicin,C12669,Demecolcine |
Microtubule Associated | Cytoskeletal Signaling |
Colcemid (NSC-3096) 是一种微管聚合抑制剂,可诱导细胞凋亡,可用于肿瘤和胚胎克隆的研究。 | |||
T13514 |
5-MethoxyPinocembroside
|
Others | Others |
5-MethoxyPinocembroside 是一种黄酮类天然产物,存在于辣木 Moringa oleifera 的叶子中。 | |||
T5710 |
Pinocembrin-7-O-β-D-glucopyranoside
Pinocembrin 7-O-beta-D-glucoside,乔松素7-O-Β-D葡萄糖苷,乔松苷 |
Others | Others |
Pinocembrin-7-O-β-D-glucopyranoside (Pinocembrin 7-O-beta-D-glucoside) 是黄酮类化合物,能够提高脂质过氧化。 | |||
TN1499 |
Cimiracemoside C
千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Cimicifugoside M |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Cimiracemoside C (Cimicifugoside M) 是在升麻中发现的一种天然产物,可激活 AMPK 并具有抗糖尿病的潜在活性。 | |||
T5S1677 |
Cimiracemoside D
|
Others | Others |
Cimiracemoside D 是一种黑升麻植物提取的天然产物。 | |||
TN2077 |
(+/-)-Pinocembrin
NSC 43318,(±)-5,7-Dihydroxyflavanone |
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
(+/-)-Pinocembrin (NSC-43318) 是一种来自腋松的天然产物,它是一种 GPR120 配体,能促进 HaCaT 细胞系的伤口愈合。 | |||
TN5509 |
(2S)-Pinocembrin 7-O-[2''-O-(5'''-O-trans-cinnamoyl)-β-D-apiofuranosyl]-β-D-glucoside
(2S)-Pinocembrin 7-O-[cinnamoyl(1→5)-β-D-apiosyl(1→2)]-β-D-glucoside |
||
(2S)-Pinocembrin 7-O-[2''-O-(5'''-O-trans-cinnamoyl)-β-D-apiofuranosyl]-β-D-glucoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5509,CAS号为 773899-29-9。 | |||
TN4792 | Pinocembrin diacetate | Others | Others |
Pinocembrin diacetate 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4792,CAS号为 111441-88-4。 | |||
T72856 |
(+)-Cembrene A
|
||
(+)-Cembrene A 是一种α-glucosidase 抑制剂,IC50为 30.31 μM。(+)-Cembrene A 对人正常肝细胞 (LO2) 无毒性。 | |||
TN4791 |
Pinocembrin 7-acetate
|
Others | Others |
Pinocembrin 7-acetate has antitumor activity. | |||
T83379 |
2-Hydroxypinocembrin
|
||
2-Hydroxypinocembrin 是一种具有 C-糖基转移酶活性的2-羟基黄烷酮类黄酮底物。 | |||
TN4423 |
Laxiracemosin H
|
Others | Others |
Laxiracemosin H is a natural product from Dysoxylum lenticellatum. | |||
T72742 |
(-)-Pinocembrin
(-)-乔松素 |
||
(-)-Pinocembrin 对 H37Ra 结核分枝杆菌展示了抗菌活性,无论是休眠还是活跃期,其 IC50 值分别为1.11 mg/mL 和 1.21 mg/mL。作为一种抗增殖剂,(-)-Pinocembrin 对于 THP-1、A549、Panc-1、HeLa 和 MCF7 细胞系,IC50 值范围为 1.88 至 11.00 mg/mL。 | |||
T3815 |
Isoscopoletin
异莨菪亭,7-Methoxyesculetin,6-Hydroxy-7-methoxycoumarin |
Others; HBV | Microbiology/Virology; Others |
Isoscopoletin (7-Methoxyesculetin) 是艾叶中的一种活性成分。它具有显著的细胞增殖抑制作用,对人类 CCRF-CEM 白血病细胞和耐药亚系 CEM/ADR5000 作用的 IC50值分别为 4.0 μM 和 1.6 μM。它具有抑制 HBV 复制的活性。 | |||
TN6512 |
Tectol
|
Transferase; Parasite | Metabolism; Microbiology/Virology |
Tectol 是从Lippia sidoides 中分离的,对人白血病细胞株 HL60 和 CEM 具有显著的抑制作用。它是法尼基转移酶抑制剂,在人和布氏锥虫的IC50分别为 2.09 和 1.73 μM。它具有抗疟原虫活性,是一种中等活性的生长抑制剂,IC50 为 3.44±0.20μM。 | |||
TN1674 |
Garcinone D
伽升沃 D |
Reactive Oxygen Species; Nrf2; STAT | Immunology/Inflammation; JAK/STAT signaling; Metabolism; NF-κB; Stem Cells |
Garcinone D 是来自山竹的一种呫吨酮,可促进 C17.2 神经干细胞的增殖。它以浓度和时间依赖的方式增加磷酸化信号转导和转录激活因子 3 (p-STAT3)、Cyclin D1 和核因子红细胞 2 相关因子 (Nrf2)、以及血红素加氧酶-1 (HO-1) 的蛋白质水平。 | |||
TN4492 | Mangostanol | AChR | Neuroscience |
Mangostanol is an acetylcholinesterase (AChE) selective inhibitor.Mangostanol has anti-cancer activity, it shows significant activities against the CEM-SS cell line, with IC50 values of 9.6 microg/ml. | |||
TN3968 | Epifriedelanol acetate | Others | Others |
Epifriedelanol exhibits antibacterial activities. It also can reduce cellular senescence in human primary cells and may be used to develop dietary supplements or cosmetics that modulate tissue aging or aging-associated diseases. Epifriedelanol and friedel | |||
TN3438 | Arborinine | HCV Protease; Antifection | Microbiology/Virology; Proteases/Proteasome |
Arborinine shows mild in vitro antibacterial activity, it possesses moderate levels of anti-hepatitis C virus(HCV) activities with the IC50 values being 6.4 ± 0.7 ug/ml. Arborinine shows antifeedant activity against Spodoptera frugiperda. Arborinin shows |