90
33
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8549 |
HEPES
|
Others | Others |
HEPES 是两性离子化学缓冲剂,在 pH 值为 6.8 至 8.2 时为有效的缓冲液,广泛应用于细胞培养。它是溶酶体生物发生的有效诱导剂。 | |||
T3478 |
Ro 67-7476
|
GluR | Neuroscience |
Ro 67-7476 是mGluR1的正变位调节剂,能增强表达 rat mGluR1a 的 HEK293 细胞中谷氨酸诱导的钙释放,EC50为 60.1 nM。它是 P-ERK1/2 激动剂,可以在外源添加谷氨酸的情况下激活 ERK1/2 磷酸化 (EC50=163.3 nM)。 | |||
T2431 |
ID-8
ID8 |
DYRK | Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors |
ID-8 是 DYRK 抑制剂,长时间培养能够维持胚胎干细胞的自我更新。 | |||
T67854 |
BAS 00489700
|
Others | Others |
BAS 00489700是一种N-UTR 相互作用抑制剂。BAS 00489700抑制培养细胞中的病毒复制。 | |||
T14181 |
Alizarin Red S sodium
ARS sodium,茜素红钠盐 |
Others | Others |
Alizarin Red S sodium (ARS sodium) 是一种蒽醌类染料,在检测细胞培养中的钙沉积具有广泛的应用。 | |||
T38509 |
MOPS
3-(N-Morpholino)propanesulfonic acid,3-吗啉丙磺酸,3-Morpholinopropanesulfonic acid,4-Morpholinepropanesulfonic acid,Morpholinopropane sulfonic acid |
Others | Others |
MOPS(Morpholinopropane sulfonic acid),作为一种广泛应用的生物缓冲剂,有效调节哺乳动物细胞培养基的pH值。 | |||
T64679 |
Calcium chloride
|
Others | Others |
Calcium chloride 常用于细胞培养研究,如用作 DMEM 培养基中的钙补充剂,也可以用于制备合成盐水溶液。 | |||
TP1125 |
Insulin(cattle)
牛胰岛素,Insulin from bovine pancreas,胰岛素 |
IGF-1R | Tyrosine Kinase/Adaptors |
Insulin cattle (Insulin from bovine pancreas) 是一种在胰腺 β 细胞中产生的两链多肽激素,在很多哺乳动物细胞培养体系中用作生长因子。 | |||
T41195 |
FFN 206 dihydrochloride
|
||
FFN 206 dihydrochloride 是一种荧光VMAT2底物,可用于检测细胞培养中的VMAT2亚细胞位置,对DAT 没有显示出可检测的抑制作用。 | |||
T9916 |
Alirocumab
|
Others | Others |
Alirocumab 是 PCSK9的人单克隆抗体。它能够特异性结合肝脏低密度脂蛋白 (LDL) 受体的下调剂 PCSK9,增强肝脏结合 LDL-胆固醇 (LDL-C) 的能力,降低血液中的 LDL-C 水平。它可用于研究高胆固醇血症。 | |||
T40112 |
PROTAC PD-1/PD-L1 degrader-1
PROTAC PD-1/PD-L1 degrader-1 |
PROTACs | PROTAC |
PROTAC PD-1/PD-L1 degrader-1, a Cereblon E3 ligand-based compound, is a PD-1/PD-L1 PROTAC that effectively inhibits the interaction between PD-1 and PD-L1 with an IC50 value of 39.2 nM. It successfully restores the suppressed immune response in a co-culture model consisting of Hep3B/OS-8/hPD-L1 cells and CD3 T cells. Additionally, this compound moderately decreases PD-L1 protein levels through a lysosome-dependent mechanism. | |||
T67797 |
DDG-39
1-(2,3-dideoxy-2-fluoropentofuranosyl)cytosine |
Antiviral; HBV; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
DDG-39 (1-(2,3-dideoxy-2-fluoropentofuranosyl)cytosine)具有抗病毒活性,在细胞培养中具有有效的选择性抗 HIV-1 和HBV 活性。平均抗病毒 IC50为0.61μM。 | |||
T33519 |
MTOB
α-keto-γ-Methylthiobutyric acid,4-甲硫基-2-氧丁酸钠,KMBA,MTOB salt,4-methylthio 2-oxobutyric acid |
Others | Others |
MTOB (α-keto-γ-Methylthiobutyric acid) 是 c 末端结合蛋白 (CtBP) 的底物,可干扰 CtBP 在细胞培养物和小鼠中的致癌活性。它还积极调节 TCF-4 信号传导,导致癌症干细胞 (CSC) 生长和自我更新。 | |||
T22839 |
HEPES Sodium
|
Others | Others |
HEPES Sodium salt 是一种非挥发性两性离子化学缓冲剂。HEPES 钠盐在细胞培养中有着广泛的应用。HEPES Sodium salt 在 pH 6.8至8.2时有效。HEPES Sodium salt 也诱导溶酶体的生物发生。 | |||
T19820 |
MOPS sodium salt
MOPS-Na,3-(N-morpholino)propanesulfonic acid sodium salt,3-吗啉丙磺酸钠盐,Sodium 3-Morpholinopropanesulfonate,4-Morpholinepropanesulfonic acid, sodium salt |
Others | Others |
MOPS sodium salt (MOPS-Na) 在生物学中常用作缓冲剂。其中MOPS 缓冲液能使哺乳动物细胞培养基的 pH 值保持稳定。 | |||
T6229 |
Daclatasvir
Daklinza,达卡他韦,EBP 883,达拉他韦,BMS-790052 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Daclatasvir (EBP 883) 是一种高度选择性的 HCV NS5A 抑制剂,EC50 为 9-50 pM,适用于细胞培养中的多种 HCV 复制子基因型和 JFH-1 基因型 2a 感染性病毒。 | |||
T37173 |
MPro Inhibitor 11a
|
||
MProinhibitor 11a is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.053 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-infected Vero E6 cells (EC50= 0.53 μM). MProinhibitor 11a also reduces viral RNA copy numbers in the same model when used at concentrations ranging from 1.85 to 50 μM. 1.Dai, W., Zhang, B., Jiang, X.-M., et al.Structure-based design of antiviral drug candidates targeting the SARS-... | |||
T40545 |
MES
2-Morpholinoethanesulphonic acid,4-Morpholineethanesulfonic acid |
Others | Others |
MES (2-Morpholinoethanesulphonic acid) (2-Morpholinoethanesulphonic acid) 是一种两性离子缓冲液,在 pH 值 5.5-7.7 范围内有效。MES 作为一种 Good's 缓冲液,广泛应用于植物培养基、试剂溶液和生理实验中调节 pH 值。 | |||
T10893 |
CS-722 Free base
|
Others | Others |
CS-722 Free base是一种合成的中枢作用肌肉松弛剂,它展现出肌肉松弛效果并抑制脊髓反射。可能通过限制钠和钙流动,从而在海马培养物中减少自发的抑制性和兴奋性突触后电流。 | |||
T17197 |
UCL 2077
|
||
UCL 2077 是癫痫相关 KCNQ 通道的亚型选择性阻滞剂,也是一种选择性慢后超极化通道阻滞剂,在培养的海马神经元中 IC50 为 500 nM,对 Ca2+ 通道、动作电位、输入电阻的影响小 ,以及超极化后的介质。 | |||
TP1895L1 |
KYL acetate(676657-00-4 free base)
|
Ephrin Receptor | Tyrosine Kinase/Adaptors |
KYL acetate(676657-00-4 free base) 是EphA4受体酪氨酸激酶抑制剂(Kd = 0.8 μM);抑制 EphA4-EphrinA5 相互作用 (IC50 = 6.34 μM)。防止 AβO 诱导的突触损伤、树突棘丢失并防止海马 CA3-CA1 传输中 LTP 的阻断。在细胞培养基中表现出较长的半衰期(在 PC3 和 C2C12 培养基中分别为 8 和 12 小时)。它有神经保护作用。 | |||
T4503 |
Talniflumate
Somalgen,他尼氟酯 |
Chloride channel; COX; N-Acetylglucosaminyltransferase; Anion Exchanger | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Talniflumate (Somalgen) 是一种钙激活氯离子通道 (hCLCA1/mCLCA3) 阻滞剂,可减少动物模型和细胞培养中的粘蛋白合成和释放。它通过抑制环氧合酶,并抑制 Cl-/HCO3- 交换活性,具有抗炎作用。它还增加了远端肠梗阻综合征囊性纤维化小鼠模型的存活率。 | |||
T60013 |
GA-017
|
Others | Others |
GA-017是一种有效的选择性 LATS1和 LATS2(大型肿瘤抑制激酶 1/2) 抑制剂,其 IC50值分别为 4.10 和 3.92 nM。GA-017 是细胞增殖的激活剂。GA-017 促进 YAP/TAZ 激活和核转位。GA-017 在 3D 培养条件下促进细胞生长。GA-017 增强小鼠肠道类器官的离体形成。 | |||
T7042 |
1,5-Isoquinolinediol
|
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
1,5-Isoquinolinediol 是一种多聚(ADP-核糖)合成酶抑制剂,对PARP1的IC50值为 0.39 µM。它用于研究 PARP1 在 DNA 修复和氧化应激诱导的细胞死亡中的作用。 | |||
T12610L |
3-Hydroxy Midostaurin
CGP52421 |
FLT | Angiogenesis; Tyrosine Kinase/Adaptors |
3-Hydroxy Midostaurin (CGP 52421), a metabolite of PKC412, effectively inhibits FMS-like tyrosine kinase-3 (FLT3) autophosphorylation with IC50s of approximately 132 nM and 9.8 μM in culture medium and plasma, respectively. 3-Hydroxy Midostaurin is less selective but more cytotoxic than PKC412[1]. | |||
T20130 |
Elastatinal
BRN0873543,BRN 0873543,BRN-0873543 |
||
Elastatinal is an elastase inhibitor. It is found in culture filtrates of various species of actinomyces. | |||
T1720L |
Amfenac
NSC309467,NSC-309467,NSC 309467 |
||
Amfenac promotes apoptosis in ARPE-19 cell culture. | |||
T32749 |
Liga 20
Liga-20,Liga20 |
||
Liga 20 is a semisynthetic GM1 ganglioside with N-dichloroacetylsphingosine that protecting neurons in culture against glutamate toxicity. | |||
T35320 |
Zygosporin D
Deactylzygosporin A |
||
Zygosporin D is one of the cytochalasins was isolated from the culture filtrate of the fungus Metarrhizium anisopliae. | |||
T25038 |
Aldgamycin E
|
||
Aldgamycin E is a neutral macrolide antibiotic agent from culture filtrates of Streptomyces lavendulae. Methanolysis produces methyl algarosides A & B. | |||
T26416 |
A 33853
A-33853,A33853 |
||
A 33853 is an antibiotic isolated from culture broth of Streptomyces sp. | |||
T27394 |
Furalazine
Furalazinum,Panfuran,Nifuralazinum,NFT |
||
Furalazine is an antimicrobial agent. Furalazine was more effective in reducing the duration of positive stool culture than chloramphenicol. It may be potentially used in the treatment of cholera. | |||
T31790 |
FFN200 dihydrochloride
FFN200 HCl,FFN200,FFN 200,FFN-200 |
||
FFN200 is a vesicular monoamine transporter 2 (VMAT2) substrate that selectively traces monoamine exocytosis in both neuronal cell culture and brain tissue. | |||
T24366 |
L 870810
L-870,810,L870810,L 870,810,L870,810,L-870810 |
||
L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties. | |||
T28476 |
Pyrroxamycin
LL-F42248-alpha,Dioxapyrrolomycin,AL-R2081 |
||
Pyrroxamycin is a new antibiotic. Pyrroxamycin was isolated from the culture broth of Streptomyces sp. S46506. Pyrroxamycin is active against Gram-positive bacteria and dermatophytes. | |||
T24432 |
MB21
MB-21,MB 21 |
||
MB21 is a dengue type 2 protease inhibitor that acts by inhibiting each one of the four serotypes of dengue viruses in infected cells in culture. | |||
T31784 |
Ferric citrate
JTT 751 |
||
Ferric citrate as a source of iron used in cell culture applications can provide iron with a less toxic form compared to free iron salts. | |||
T71073 |
Tan 931
|
||
Tan 931 is a nonsteroidal aromatase inhibitor that was first isolated from the culture filtrate of a soil isolate fungus, No. 8974 | |||
T11795 |
L-4-Oxalysine hydrochloride
|
Others | Others |
L-4-Oxalysine hydrochloride has shown antitumor activities, is a natural product isolated from the culture media of Streptomyces roseovirdofuscus in China. | |||
T70878 |
P516-0475
|
||
P516-0475 is a novel chemical inducer of Streptococcus quorum sensing acts by inhibiting the pheromone-degrading endopeptidase PepO. This compound induces quorum sensing by stabilizing SHP pheromones in culture. | |||
T69782 | GS-9822 | ||
GS-9822 is a novel LEDGIN, an inhibitor that targets the binding pocket of LEDGF/p75 which is a cellular cofactor that substantially contributes to HIV integration site selection, displaying a block-and-lock phenotype in cell culture. | |||
T28311 |
PD 116152
PD116,152,PD 116,152,PD116152,PD-116,152,PD-116152 |
||
PD 116152 is a highly substituted phenazine with antitumor activity isolated from the culture broth of a Streptomyces sp. The antitumor activity versus murine P388 leukemia is T/C 149. PD 116152 is selectively active versus the bacterium Streptococcus pne | |||
T25849 |
Naftoxate
Naftoxatum,Naftoxato |
||
Naftoxate is an antimicotic. It is effective against both gram-positive and gram-negative bacteria as well as yeasts and other fungi in plant cell culture. | |||
T36751 |
Dihydroxy Melphalan
|
||
Dihydroxy melphalan is an inactive degradation product of melphalan . It is formed by the hydrolysis of melphalan via the intermediate monohydroxy melphalan in aqueous solutions, including cell culture medium and human plasma. | |||
T36436 |
Spergualin trihydrochloride
|
||
Spergualin trihydrochloride is a natural product that first identified as an antibiotic from culture filtrates of Bacillus laterosporus BMG162-aF2[1]. Spergualin trihydrochloride derivatives likely acts as Hsp70 modulators[1]. [1]. Srikanth Patury, et al. Pharmacological Targeting of the Hsp70 Chaperone. Curr Top Med Chem. 2009;9(15):1337-51. | |||
T38823 |
sulfo-DGN462 sodium
sulfo-DGN462 sodium |
||
Sulfo-DGN462 sodium undergoes degradation to DGN462 when subjected to culture medium and plasma. DGN462, a highly effective DNA-alkylating agent, exhibits anti-tumor properties that are particularly active against acute myeloid leukemia (AML). | |||
T71487 |
WRR-483
|
||
WRR-483, an analogue of K-11777, is a potent and selective cysteine protease inhibitor with trypanocidal activity in cell culture and animal model with comparable efficacy to K11777. WRR-483 demonstrates good potency against cruzain with sensitivity to pH conditions and high efficacy in the cell culture assay. Furthermore, WRR-483 also eradicates parasite infection in a mouse model of acute Chagas' disease. WRR-483 binds covalently to the active site cysteine of the protease in a similar manner... | |||
T65782 |
HEPBS
|
Others | Others |
HEPBS 是一种两性离子生物缓冲剂,其 pH 范围在7.6到9.0之间。HEPBS 可用于细胞的培养和其他细胞实验。 | |||
T27367 |
FR 900490
BMY 28700,FR-900490,FR900490 |
||
FR 900490 is an immunoactive substance produced by a fungus Discosia sp. F-11809. In vitro FR-900490 restores the colony forming units in culture (cfu-c) in bone marrow cells, which were suppressed by immunosuppressive factor obtained from the serum of sa | |||
T71930 |
aPKC-I
|
||
aPKC-I is an inhibitor of atypical protein kinase C (aPKC ) which inhibits both PKCζ and PKCι with high specificity and prevents VEGF-induced endothelial permeability in cell culture and in vivo, thereby blocking ischemia-reperfusion (IR)-induced permeability. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2A2476 |
L-Hydroxyproline
羟脯氨酸,trans-4-Hydroxy-L-proline,L-Hydroxyprolin,Trans-4-Hydroxyproline |
Endogenous Metabolite | Metabolism |
L-Hydroxyproline (L-Hydroxyprolin) 是羟脯氨酸的异构体之一,是药物生产中有用的手性结构单元。 | |||
T4S1521 |
1,4-Dicaffeoylquinic acid
1,4-二咖啡酰奎宁酸,洋蓟素 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
1,4-Dicaffeoylquinic acid 是一种苯丙素类物质,从苍耳子中获得,可以减少 LPS 诱导的 TNF-α 的生成,具有抗炎活性。 | |||
T39007 |
3,4-Dimethoxybenzamide
|
Others | Others |
3,4-Dimethoxybenzamide 是分离自Streptoverticillium morookaense 固体培养物的酰胺。它是制备盐酸伊托必利的起始原料。 | |||
T4915 |
β-Glycerophosphate disodium salt hydrate
|
Phosphatase; Endogenous Metabolite | Metabolism |
β-Glycerophosphate disodium salt hydrate 是一种磷酸酶抑制剂,是内源性代谢产物的一种。 | |||
T39887 |
(S)-3-(4-Hydroxyphenyl)lactic acid
(S)-3-(4-羟苯基)乳酸,(S)-3-(4-Hydroxyphenyl)lactic acid,(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid |
Others | Others |
(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid ((S)-3-(4-Hydroxyphenyl)lactic acid) 是分离自间肠隐球菌培养基的代谢物,具有高的 DPPH 清除自由基活性和抗氧化活性。 | |||
T60789 |
L-Cystine dihydrochloride
|
||
L-Cystine dihydrochloride 是合成谷胱甘肽 (GSH) 的含硫前体。L-Cystine dihydrochloride 的稳态对谷胱甘肽的功能很重要。L-Cystine dihydrochloride 可用作细胞培养组分。 | |||
T20945 |
2,4-D
Hedonal,Macondray,2,4-D acid,Chloroxone,2,4-二氯苯氧乙酸 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2,4-Dichlorophenoxyacetic acid (Hedonal) 是一种合成生长素,用作植物生长调节剂,也用作植物细胞培养基中的补充剂。它是除草剂中的一种活性成分,用于破坏肌动蛋白细胞骨架,以控制根系伸长和细胞生成。 | |||
T20879 |
Tacrolimus monohydrate
FK-506,FR 900506,Prograf,FR900506,Tacrolimus hydrate,LCP-Tacro,他克莫司一水合物,FK 506 |
Phosphatase; Others; Antibacterial; Antibiotic; Autophagy | Autophagy; Metabolism; Microbiology/Virology; Others |
Tacrolimus monohydrate (LCP-Tacro) 是大环内酯类化合物,它与 FK506 结合蛋白 (FKBP) 结合形成复合物并抑制钙调神经磷酸酶,从而抑制 T 淋巴细胞信号转导和 IL-2 转录。具有强免疫抑制特性。 | |||
T3889 |
Platycodin D
|
Prostaglandin Receptor; AMPK | Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; PI3K/Akt/mTOR signaling |
Platycodin D 是从桔梗中分离得到的一种皂苷类天然产物,是AMPKα的激活剂,具有抗肥胖活性。它可刺激 TNF-α 合成或抑制 TNF-α mRNA 的降解。 | |||
T4918 |
DL-Glyceraldehyde
Glyceric aldehyde,DL-甘油醛晶体 |
Reductase | Endocrinology/Hormones; Metabolism |
DL-Glyceraldehyde (Glyceric aldehyde) 是由酶甘油醛脱氢酶的作用产生的,该酶使用 NADP 作为辅因子将甘油转化为甘油醛。它是一种高活性化合物,可以修饰和交联蛋白质。 | |||
T36585 |
Isodeoxycholic Acid
isoDCA |
Chloride channel; Antibacterial | Membrane transporter/Ion channel; Microbiology/Virology |
Isodeoxycholic Acid 是一种胆汁酸,由肠道细菌通过脱氧胆酸的表聚作用形成。Isodeoxycholic acid 的临界胶束浓度高于二氯苯甲醚,这表明它的去污活性降低了,而且在抑制七种肠道共生细菌生长方面的活性低于二氯苯甲醚。Isodeoxycholic Acid(0.1%)能抑制几种艰难梭菌菌株在牛磺胆酸诱导下的孢子萌发,并能降低艰难梭菌培养上清对 Vero 细胞的细胞毒性。在高脂饮食诱发肥胖的大鼠模型中,血浆中的Isodeoxycholic acid 水平比正常饮食的大鼠低。 | |||
T38579 |
Rutarensin
|
||
Rutarensin is a phenolic compound found in Ruta chalepensis cell culture. | |||
TN6688 |
Cyclo(Ala-Tyr)
|
||
Cyclo(Val-Tyr) is a product from the culture of Pseudomonas putida. | |||
T20541 |
Phosphoramidon
|
||
Phosphoramidon is a membrane metallo-endopeptidase & endothelin-converting enzyme inhibitor and thermolysin inhibitor, which is obtained from culture filtrate of Streptomyces tanashiensis. | |||
TN4085 |
Fupenzic acid
|
Others | Others |
Fupenzic acid shows a significant decrease in intracellular melanin content in B16-F10 cells, and in culture media melanin. | |||
T20628 | Kifunensine | ||
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, may serve as a key inhibitor of glycoprotein biosynthesis. Its inhibitory effect may lead to high mannose glycoproteins in cell culture. | |||
TN3547 |
Bullatantriol
|
Antifection | Microbiology/Virology |
Bullatantriol has a stimulative effect on significantly proliferation and differentiation of culture osteoblasts. It may have weak antibacterial activities. | |||
TN4328 |
Isosativenediol
|
Others | Others |
Isosativenediol is a natural product from the culture filtrates of a Bipolaris species pathogenic to Johnson grass. | |||
TN4716 |
Oplodiol
|
Influenza Virus | Microbiology/Virology |
Oplodiol exhibits noteworthy anti-plasmodial activity against Plasmodium falciparum strains. Oplodiol has a stimulative effect on significantly proliferation and differentiation of culture osteoblasts; it also shows moderate cytotoxic effects on the human | |||
TN2841 | 2alpha,9alpha,11-Trihydroxy-6-oxodrim-7-ene | Others | Others |
2alpha,9alpha,11-Trihydroxy-6-oxodrim-7-ene is a natural product from the culture medium of the marine-derived fungus Aspergillus insuetus (OY-207). | |||
T81735 |
Mycestericin C
|
||
Mycestericin C, 分离自 Mycelia sterilia ATCC 20349 的培养液, 能在小鼠同种异体混合淋巴细胞反应中抑制淋巴细胞的增殖。 | |||
T75534 | Maniwamycin E | ||
Maniwamycin E,一种耐热链霉菌培养提取物中分离得到的马尼瓦霉素衍生物,展示了对SARS-CoV-2和H1N1流感病毒的抗病毒活性。 | |||
TN2792 |
2-Oxopomolic acid
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2-Oxopomolic acid shows cytotoxic activity, it shows a significant decrease in intracellular melanin content in B16-F10 cells, and in culture media melanin. 2-Oxopomolic acid shows radical-scavenging activities similar to that of the reference antioxidant | |||
T36295 | Echistatin TFA | ||
Echistatin TFA, the smallest active RGD protein belonging to the family of disintegrins that are derived from snake venoms, is a potent inhibitor of platelet aggregation. Echistatin is a potent inhibitor of bone resorption in culture. Echistatin is a potent antagonist of αIIbβ3, αvβ3 and α5β1[1][2][3][4]. [1]. J Musial, et al. Inhibition of platelet adhesion to surfaces of extracorporeal circuits by disintegrins. RGD-containing peptides from viper venoms. Circulation. 1990 Jul;82(1):261-73.[2]. ... | |||
T81016 |
Terrelumamide A
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Terrelumamide A是一种带有lumazine结构的肽类化合物,从海洋真菌Aspergillus terreus的培养物中提取分离得到。该化合物因增强胰岛素敏感性而显示出药理作用,并在DNA序列识别方面具有潜在应用价值。 | |||
T81676 |
NG-012
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NG-012为一种神经生长因子(NGF)增强剂,来源于Penicillium verruculosum F-4542的培养液。该化合物能在大鼠嗜铬细胞瘤细胞系(PC12)中提升NGF引导的神经突生长效应。 | |||
T70355 |
Flutimide
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Flutimide是一种针对流感病毒核酸内切酶的选择性抑制剂,具有3 μM的IC50值,表现出细胞培养中的抗病毒活性,适用于流感等急性传染性呼吸道疾病的研究。 | |||
T74196 |
Inophyllum B
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Inophyllum B ((+)-Inophyllum B) 是一种有效的HIV 逆转录酶 (Reverse Transcriptase) 抑制剂,IC50为 38 nM。Inophyllum B 在体外细胞培养中抑制HIV-1(IC50=1.4 μM)。Inophyllum B 可从非洲大蜗牛Achatina fulica 的丙酮提取物中分离得到。 | |||
TN3753 |
Dalbergioidin
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Tyrosinase; ROS; Akt; PI3K; TGF-beta/Smad | Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Dalbergioidin exhibits tyrosinase inhibitory activity with an IC50 of 20 mM. It shows a melanin biosynthesis inhibition zone in the culture plate of Streptomyces bikiniensis that has commonly been used as an indicator organism. Dalbergioidin protects MC3T3-E1 osteoblastic cells against H2O2-induced cell damage through activation of the PI3K/AKT/SMAD1 pathway, suggests that it may be useful in bone metabolism diseases, particularly osteoporosis. Dalbergioidin also ameliorates doxorubicin-induced ... | |||
TN2533 |
1-Hydroxy-2,3,4,7-tetramethoxyxanthone
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5-HT Receptor | GPCR/G Protein; Neuroscience |
1-Hydroxy-2,3,4,7-tetramethoxy-xanthone has vasodilatory action, it can cause vasodilation in the coronary artery pre-contracted with 1uM 5-hydroxytryptamine (5-HT), with the EC 50 value of 6.6±1.4 uM. 1-Hydroxy-2,3,4,7-tetramethoxyxanthone can effectivel | |||
TN2534 |
1-Hydroxy-2,3,5-trimethoxyxanthone
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IκB/IKK; Calcium Channel; NOS; 5-HT Receptor; COX | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB |
1-Hydroxy-2,3,5-trimethoxyxanthone (HM-1) has vasodilator action ,which involves both an endothelium-dependent mechanism involving NO and an endothelium-independent mechanism by inhibiting Ca(2+) influx through L-type voltage-operated Ca(2+) channels; a minor contribution to the effects of HM-1 may be related to inhibition of the protein kinase C-mediated release of intracellular Ca(2+) stores. HM-1,at the concentration of 1 ug/mL, can effectively inhibit the osteoclast differentiation in a co-c... | |||
T81201 |
Sartorypyrone B
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Sartorypyrone B为Chevalone C的2β-乙酰氧基衍生物,由海绵源真菌Neosartorya tsunodae(KUFC 9213)的培养物中乙酸乙酯提取得到。该化合物对MCF-7、NCI-H460和A375-C5细胞系展示出较强的生长抑制活性,GI50s值分别为17.8、20.5和25.0 μM,显示其在乳腺癌、非小细胞肺癌和黑色素瘤研究中的应用潜力。 | |||
T15637 |
K-252b
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PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
K-252b is an indolocarbazole isolated from the actinomycete Nocardiopsis and is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in culture because it can’t pass through the cell membrane freely. |