77
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8513 |
Spastazoline
|
Others | Others |
Spastazoline 是spastin(一种微管切断AAA 蛋白) 的选择性抑制剂,对人 spastin 的IC50值为 99 nM。它不能影响重组人 VPS4 的 ATPase 活性。 | |||
T6393 |
ARQ 621
|
Kinesin | Cytoskeletal Signaling |
ARQ 621 是一种变构和选择性 Eg5 有丝分裂运动蛋白抑制剂,具有抗肿瘤活性。 | |||
T12642L |
Simurosertib
TAK-931 |
CDK | Cell Cycle/Checkpoint |
Simurosertib (TAK-931) 是一种选择性和 ATP 竞争性细胞分裂周期 7 激酶抑制剂,具有抗癌活性,IC50值小于 0.3 nM。 | |||
T21678 |
3MB-PP1
|
PLK | Cell Cycle/Checkpoint |
3MB-PP1是嘌呤类似物,是一种 Polo 样激酶 1 (Plk1) 抑制剂。在表达类似物敏感的 Plk1 等位基因的细胞中,3MB-PP1 通过靶向 Plk1 阻断有丝分裂进程和细胞分裂。3MB-PP1 特异性抑制类似物敏感的 Ssn3 (Cdk8)。3MB-PP1 抑制 Leu93 突变 Zipper-interacting protein kinase(Leu93-ZIPK),IC50为2 μM。3MB-PP1 可用于细胞分裂和白色念珠菌 (Candida albicans) 菌丝形成的研究。 | |||
T21970 |
ML-097
|
GTPase | GPCR/G Protein |
ML-097 是 Ras 相关 GTP 酶的泛激活剂。 | |||
T0849 |
Pyrimethamine
Pirimecidan,RP 4753,Pirimetamin,乙胺嘧啶 |
DHFR; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Pyrimethamine (Pirimecidan) 是一种二氢叶酸还原酶的竞争性抑制剂,用作抗疟药。 | |||
T22991 |
ML-099
|
Rho; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
ML-099 是广谱的 Ras 相关GTPases 激活剂,对Rac1、cell division cycle 42、Ras、Rab7和Rab-2A 均有激活作用。 | |||
T8586 |
cicloprofen
|
Others | Others |
cicloprofen 是细胞分裂周期 7 相关蛋白激酶(人)抑制剂。 | |||
T15141 |
DM4
Ravtansine,美登素 DM4 |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
DM4 (Ravtansine)可用于制备抗体药物偶联物,是抗微管蛋白剂。 它抑制细胞分裂。 | |||
T12642 |
(R)-Simurosertib
(R)-TAK-931 |
CDK | Cell Cycle/Checkpoint |
(R)-Simurosertib ((R)-TAK-931) 是具有 ATP 竞争作用的细胞分裂周期 7 (CDC7) 激酶的抑制剂。 | |||
T3256 |
MMAF
一甲基澳瑞他汀 F,MonoMethyl auristatin F |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
MMAF (MonoMethyl auristatin F) 是一种抗有丝分裂剂,通过阻断微管蛋白的聚合来抑制细胞分裂,用作抗肿瘤药物和抗体偶联药物的细胞毒性成分。 | |||
T3352 |
XL413
|
cholecystokinin; Casein Kinase; Pim; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic; GPCR/G Protein; JAK/STAT signaling; Metabolism; Stem Cells |
XL413 是一种口服生物可利用的细胞分裂周期 7 同源物 (CDC7) 激酶抑制剂,具有潜在的抗肿瘤活性,IC50值为 3.4 nM。它对 pMCM 的 EC50值为 118 nM,对 CK2 和 PIM1 的 IC50值分别为 215 和 42 nM。 | |||
T6897 |
Monomethyl auristatin E
一甲基澳瑞他汀E,Vedotin,MMAE |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Monomethyl auristatin E (MMAE) 是海兔毒素 10 的合成衍生物,是一种抗有丝分裂剂,通过阻断微管蛋白的聚合来抑制细胞分裂,并且还具有抑制抗体-药物偶联物的活性。 | |||
T6437 |
Cefoperazone
头孢哌酮,Cefob,Medocef |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefoperazone (Medocef) 是一种半合成的头孢菌素,有抗菌活性。 | |||
T1060 |
Flumequine
Flumigal,氟甲喹,R-802 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Flumequine (R-802) 是一种喹诺酮类抗生素,对革兰氏阳性菌和革兰氏阴性菌均有效。它是拓扑异构酶 II 抑制剂, 抑制细胞分裂,IC50值为 15 μM (3.92 μg/mL)。 | |||
T14348 |
Auristatin E
|
Microtubule Associated | Cytoskeletal Signaling |
Auristatin E 通过阻断微管蛋白的聚合来抑制细胞分裂。它是一种细胞毒性微管蛋白修饰剂,具有强效和选择性抗肿瘤活性。它是一种 MMAE 类似物,是抗体-药物偶联物中的细胞毒素。 | |||
T11929 |
M2N12
|
Phosphatase | Metabolism |
M2N12 是一种高度选择性的细胞分裂周期蛋白磷酸酶 25C 抑制剂,IC50值为 0.09 μM。它还抑制 Cdc25A 和 Cdc25B 的活性,IC50值分别为 0.53 μM 和 1.39 μM。它具有抗肿瘤活性,可研究癌症。 | |||
T1228 |
Cefonicid sodium
Monocid sodium,头孢尼西钠,Cefonicid disodium salt |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefonicid sodium (Monocid sodium) 是一种广谱头孢类抗生素, 能抑制细菌细胞壁的形成。 | |||
T1213 |
Piperacillin sodium
哌拉西林钠,Sodium piperacillin,CL227193,Piperacillin sodium salt |
Antibacterial; Antibiotic | Microbiology/Virology |
Piperacillin sodium salt(CL227193) )是一种β-内酰胺类广谱抗生素。 | |||
T2511 |
Plinabulin
普那布林,NPI-2358 |
Microtubule Associated | Cytoskeletal Signaling |
Plinabulin (NPI-2358) 是一种抗微管蛋白解聚肿瘤细胞的血管破坏剂,选择性地靶向并结合到微管蛋白的秋水仙碱结合位点,从而中断微管动力学的平衡。它对人肿瘤细胞系具有抑制作用,对 HT-29 细胞系的IC50值为 9.8 nM。 | |||
T4433 |
6-CFDA N-succinimidyl ester
Carboxyfluorescein diacetate succinimidyl |
Others | Others |
6-CFDA N-succinimidyl ester (Carboxyfluorescein diacetate succinimidyl) 能够自发且不可逆地与游离胺结合。在流式细胞术实验中用于追踪哺乳动物细胞和细菌的细胞分裂。与多种细胞透化剂结合使用,作为一种有效的、非破坏性的荧光染料,可快速检测细菌细胞。 | |||
T3661 |
Citarinostat
ACY241,HDAC-IN-2 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Citarinostat (ACY241) 是一种强效、选择性和口服组蛋白脱乙酰酶 (HDAC) 抑制剂,具有抗肿瘤活性,对 HDAC1、HDAC2、HDAC3、HDAC6 和 HDAC8 的 IC50分别为 35、45、46、2.6 和 137 nM。 | |||
T1122 |
Cephalothin sodium
头孢噻吩钠,Cefalotin sodium,Cephalothin,Cefalotin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cephalothin sodium (Cefalotin) 是一种头孢类抗生素, 具有广泛的抗菌活性,抑制革兰氏阳性和阴性菌。 | |||
T10735 |
CDK4/6/1 Inhibitor
Crozbaciclib |
CDK | Cell Cycle/Checkpoint |
CDK4/6/1 Inhibitor (Crozbaciclib) 是一种 CDK4/6 抑制剂 (IC50s: 3 and 1 nM). CDK4/6抑制剂是一类用于治疗一些类型的激素受体阳性、her2阴性乳腺癌的化合物,可阻断了乳腺癌细胞分裂和繁殖的过程。 | |||
T1600 |
Doxifluridine
Ro 21-9738,AMC 0101,5'-DFUR,5-Fluoro-5'-deoxyuridine,去氧氟尿苷 |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Doxifluridine (AMC 0101) 是一种胸苷磷酸化酶活化剂,对 PC9-DPE2细胞的 IC50为0.62 μM。它是具有抗肿瘤活性的抗肿瘤剂 5-fluorouracil (5-FU) 的氟嘧啶衍生物和口服前药。 | |||
T67509 |
Cholesteryl Hemisuccinate
Cholesterol hydrogen succinate |
Apoptosis; DNA/RNA Synthesis; Topoisomerase | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Cholesteryl Hemisuccinate (Cholesterol hydrogen succinate) 是一种经常使用在极性溶液中具有高溶解度的胆固醇类似物 ,具有保肝、抗癌和抑制肿瘤生长的作用。Cholesteryl Hemisuccinate 抑制对乙酰氨基酚 的肝毒性,并防止 AAP 诱导的肝细胞凋亡 和坏死 。Cholesteryl Hemisuccinate 抑制 DNA 聚合酶 和 DNA 拓扑异构酶 ,从而抑制 DNA 复制和修复以及细胞分裂。 | |||
T3615 |
Evofosfamide
艾伏磷酰胺,TH-302 |
Apoptosis; Others | Apoptosis; Others |
Evofosfamide (TH-302) 是一种缺氧激活前药,在缺氧 (N2) 和常氧 (21% O2) 环境下,IC50分别为 10 μM 和 1000 μM。 | |||
T1408 |
Capecitabine
Xeloda,卡培他滨,Capecitibine,Capiibine,RO 09-1978 |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Capecitabine (Capecitibine) 是一种可口服的前药,可由胸苷磷酸化酶催化转变为其活性代谢物 Fluorouracil。 | |||
T25529 |
IMM-01
|
GTPase | GPCR/G Protein |
IMM-01 是一类新型的哺乳动物透明 (mDia) 相关形式的小分子激动剂,其作用于 Rho GTPase 下游以组装肌动蛋白丝,并与微丝组织在迁移和不对称分裂过程中建立和维持细胞极性. GTP 结合的 Rho 通过破坏 DID 和 DAD 自动调节结构域之间的相互作用来激活 mDia 家族成员,从而释放 FH2 结构域以调节肌动蛋白和微管动力学。 | |||
T40443 |
JAK2-IN-6
JAK2-IN-6 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
JAK2-IN-6是一种有效的、有选择性的 JAK2抑制剂(ic50为22.86 μg/mL),是一种多取代氨基噻唑衍生物。JAK2-IN-6抑制 JAK2酶的活性 ,通过干扰与 JAK2相关的信号通路,从而对 JAK2失调的特定疾病产生治疗作用, 对 JAK1和JAK3不显示出活性。JAK2是一种参与调节细胞生长和分裂的信号通路的蛋白质。JAK2的异常激活与多种疾病有关,包括某些类型的癌症和炎症性疾病。JAK2-IN-6对癌细胞具有抗增殖活性。 | |||
T24126 |
Gyramide A
Gyramide-A |
||
Gyramide A is an inhibitor of bacterial DNA gyrase. It shows antimicrobial activity and inhibits bacterial cell division. | |||
T19830 |
Dicapthon
AC4124,AC 4124,Captex,ENT-17035,ENT 17035,AC-4124 |
||
Dicapthon is an insecticide. Dicapthon increases the occurrence of abnormal cell frequency, decreases the mitotic index, and decreases the nuclear division index. | |||
T34924 |
Triadimenol
Spinnaker,UK199,Baytan,UK 199,UK-199 |
||
Triadimenol is a systemic fungicide with a broad spectrum. It inhibits the ergosterol - and gibberellin - biosynthesis, and thus the rate of cell division. | |||
T23578 |
(S)-Gyramide A
(S)-Gyramide-A,(S)-534F6,(S)534F6,(S) 534F6 |
||
(S)-Gyramide A is a bacterial DNA gyrase inhibitor that acts by exhibiting antimicrobial activity and inhibiting bacterial cell division. | |||
T31838 |
Folic acid, methyl-
x-Methylfolic acid,x-Methyl folic acid,x-Methylpteroylglutamic acid |
||
Folic acid, methyl- is a nutrient that belongs to the vitamin B family. Folate is significant for the easy conversion of carbohydrates into glucose and is essential in red blood cell formation, cell division, detoxification, and the production of some neu | |||
T38428 |
Alisertib sodium
MLN 8237 sodium |
||
Alisertib sodium (MLN 8237) is a potent and specific inhibitor (IC50 = 1.2 nM) of Aurora A kinase, an enzyme involved in cell division. By binding to Aurora A kinase, Alisertib sodium disrupts the formation of the mitotic spindle and causes abnormal cell division. At the molecular level, it acts on the AKT/mTOR/AMPK/p38 pathway, leading to the induction of apoptosis and autophagy in leukemic cells. This compound exhibits significant antitumor activity. | |||
T70958 | Dov-Val-Dil-OH TFA | ||
Dov-Val-Dil-OH is a useful chemical intermediate for synthesis of auristatin-related compounds, such as Monomethyl auristatin E (MMAE), Auristatins are antimitotic agents which inhibits cell division by blocking the polymerisation of tubulin. | |||
T40782 | Metazachlor | ||
Metazachlor, a member of the chloroacetamide class of herbicides, acts as a long chain fatty acid synthesis inhibitor. It exerts an influence on cell division and tissue differentiation in germinating and emerging weed species. | |||
T72934 |
Epothilone E
埃博霉素E |
||
Epothilone E,作为Epothilone的衍生化合物,通过抑制微管蛋白功能来阻碍细胞分裂,从而展现出抗肿瘤活性。 | |||
T36106 |
Coumermycin A1
|
||
Coumermycin A1 is a JAK2 signal activator. Coumermycin A1 inhibits DNA Gyrase which thereby inhibits cell division in bacteria. Coumermycin A1-induced-JAK2 signal activation increases the mRNA level of SCOS2, but reducea leptin receptor mRNA level[1]. [1]. Tiantian Zhang, et al. SOCS2 Inhibits Mitochondrial Fatty Acid Oxidation via Suppressing LepR/JAK2/AMPK Signaling Pathway in Mouse Adipocytes. Research Article. | |||
T21298 |
SNS-314
SNS-314 free base,SNS314,SNS 314 |
||
SNS-314, a synthetic small molecule Aurora kinase (AK) inhibitor with potential antineoplastic activity, selectively binds and inhibits AKs A and B, resulting in the inhibition of cell division and proliferation in tumor cells that overexpress AKs. | |||
T25043 | Alestramustine | ||
Alestramustine is a cytostatic antineoplastic agent. The drug, via its active metabolites, binds to microtubule-associated proteins and β-tubulin and interferes with microtubule function, thereby suppressing cell division. Due to its estrogen moiety, Ales | |||
T11042 |
Dihydrocytochalasin B
|
Others | Others |
Dihydrocytochalasin B (H2CB) is a cell division inhibitor that changes the morphology of cells, similar to cytochalasin B. Does not inhibit glucose transport. Dihydrocytochalasin B (H2CB) disrupts the structure of actin and inhibits the ability of growth | |||
T36801 |
Binucleine 2
|
||
Binucleine 2 is an isoform-specific and ATP-competitive inhibitor of Drosophila Aurora B kinase (Ki = 0.36 μM), a kinase involved in cell division. It is specific for Drosophila Aurora B kinase, inhibiting it in a dose-dependent manner, with minimal inhibition of human or X. laevis Aurora B kinases at concentrations up to 100 μM. Binucleine 2 induces mitotic and cytokinesis defects in Drosophila Kc167 cells. It prevents Drosophila S2 cells from assembling a contractile ring during cell division ... | |||
TP2192 |
Cdk2/Cyclin Inhibitory Peptide I
|
Others | Others |
Cyclin-dependent kinase 2 also known as cell division protein kinase 2. The protein encoded by this gene is a member of the cyclin-dependent kinase family of Ser/Thr protein kinases. This protein kinase is highly similar to the gene products of S. cerevis | |||
T70942 |
AM-8508
|
||
AM-8508 is a potent and selective PI3Kδ inhibitor. AM-8508 showed good cellular potency (in vitro pAKT IC50 = 4.6 nM ). AM-8505 xhibited excellent HWB potency (HWB (pAKT) IC50 = 2.7 nM). AM-8508 inhibit KLH-specific antibodies in animal models, signifying its potential for the treatment of human inflammatory diseases. PI3Kα and PI3Kβ are ubiquitously expressed and play a role in cell growth, division, and survival. | |||
T69091 |
CBP501
|
||
CBP501 is a peptide with G2 checkpoint-abrogating activity. G2 checkpoint inhibitor CBP501 inhibits multiple serine/threonine kinases, including MAPKAP-K2, C-Tak1, and CHK1, that phosphorylate serine 216 of the dual-specific phosphatase Cdc25C (cell division checkpoint 25 C); disruption of Cdc25C activity results in the inhibition of Cdc25C dephosphorylation of the mitotic cyclin-dependent kinase complex Cdc2/cyclin B, preventing entry into the mitotic phase of the cell cycle. | |||
T74555 |
EDA-DA
|
||
EDA-DA 是一种 N 末端标记的二肽探针,可用于标记细菌的肽聚糖 (PG)。肽聚糖 (PG) 是绝大多数细菌细胞壁中的一种基本结构,对于分裂和维持细胞形状和静水压力至关重要。 | |||
T70808 |
Cabazitaxel-d6
|
||
Cabazitaxel-d6 is a deuterium labeled cabazitaxel. Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel binds to and stabilizes tubulin, resulting in the inhibition of microtubule depolymerization and cell division, cell cycle arrest in the G2/M phase, and the inhibition of tumor cell proliferation. Unlike other taxane compounds, this agent is a poor substrate for the membrane-associated, multidrug resistance... | |||
T70748 |
Bisthianostat
|
||
Bisthianostat, also known as CF367 or CF367;-C, is a novel Orally Efficacious Pan-HDAC Inhibitor. Bisthianostat selectively binds to and inhibits HDACs, which inhibits deacetylation of histone proteins and leads to the accumulation of highly acetylated histones. This may result in an induction of chromatin remodeling, the inhibition of tumor oncogene transcription, and the selective transcription of tumor suppressor genes. This prevents cell division, induces cell cycle arrest and apoptosis. Thi... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13818 |
Phytohemagglutinin
PHA-M,植物血球凝集素,PHA,植物血凝素 |
Apoptosis | Apoptosis |
Phytohemagglutinin (PHA-M) 是一种普通豆菜豆的主要种子凝集素,聚集在子叶的薄壁细胞中。它是一种 T 细胞激活剂,能够刺激人单核白细胞,可诱导 ChAT mRNA 表达,增强 ACh 合成。 | |||
T8211 |
(±)-Decursinol
紫花前胡醇,3',4'-dihydro-3'-hydroxy-Xanthyletin |
Others; Antibacterial | Microbiology/Virology; Others |
(±)-Decursinol (3',4'-dihydro-3'-hydroxy-Xanthyletin) 是来自当归的一种 FtsZ 抑制剂,抑制 B. anthracis 的 FtsZ 聚合,IC50为 102 μM。 | |||
T2942 |
Psoralen
Ficusin,Furocoumarin,补骨脂素,psoralene |
Apoptosis; Influenza Virus; HIV Protease; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Psoralen (Ficusin) 是从补骨脂种子中提取的一种香豆素。它具有如抗癌、抗氧化、抗抑郁、抗癌、抗菌、抗病毒等多种生物学特性。 | |||
T14304 |
Aphidicolin
|
Others | Others |
Aphidicolin is a potent inhibitor of cellular deoxyribonucleic acid synthesis and inhibits the growth of herpes simplex virus[2]. Aphidicolin is an inhibitor of DNA polymerase α and δ, prevents mitotic cell division by interfering with the activity of DNA | |||
T3151 |
Brassinolide
Brassin lactone,24-Epibrassinolide,芸苔素内酯 |
Apoptosis; Others | Apoptosis; Others |
Brassinolide (Brassin lactone) 是一种植物生长调节剂,可调节植物细胞伸长。 | |||
TMS2181 |
trans-Zeatin
(E)-Zeatin,玉米素 |
ERK; MEK; Endogenous Metabolite | MAPK; Metabolism |
trans-Zeatin ((E)-Zeatin) 是植物细胞分裂素,可抑制紫外线诱导的MEK/ERK 的活化,在细胞生长、分化和分裂中起着重要的作用。 | |||
TMS2182 |
trans-Zeatinriboside
Ribosylzeatin,Zeatin Riboside,Trans-Zeatin Riboside,玉米素核苷 |
Others | Others |
trans-Zeatinriboside (Ribosylzeatin) 是一种细胞分裂素前体,是木质素导管中主要的长距离信号形式,能够调节叶片大小和分生组织活性相关形状。 | |||
T7132 |
(Rac)-Brassinazole
BRASSINAZOLE,3-(4-氯苯基)-1-甲基-1-苯基-2-(1,2,4-三唑-1-基)-1-丙醇,(Rac)-芸苔素唑 |
P450 | Metabolism |
(Rac)-Brassinazole 是三唑型化合物,是油菜素甾醇 (BR) 生物合成抑制剂。它能够增强 CYP90B 在 BR 生物合成中的抑制作用。 | |||
T1004 |
6-Benzylaminopurine
6-苄氨基嘌呤,6-BAP,N6-Benzyladenine,BA,Benzyladenine |
Others | Others |
6-Benzylaminopurine (6-BAP) 是一种细胞分裂素,能够通过刺激细胞分裂引起植物生长和发育,抑制呼吸激酶,从而延长绿色蔬菜的保鲜。 | |||
TMS2179 |
Zeatin
玉米素 |
Others | Others |
Zeatin 是一种来源于腺嘌呤的细胞分裂素。Zeatin 是在玉米属的未成熟玉米粒中发现的。它促进侧芽的生长,当喷洒在分生组织上时会刺激细胞分裂,从而产生更浓密的植物。 | |||
T5088 |
3-Indoleacetic acid sodium
Indole-3-Acetic Acid sodium salt,Sodium 2-(1H-indol-3-yl)acetate,IAA sodium salt,吲哚乙酸钠,Heteroauxin sodium salt |
Others; Endogenous Metabolite | Metabolism; Others |
3-Indoleacetic acid sodium (Heteroauxin sodium salt) 是一种天然存在的植物生长素类激素。能刺激细胞伸长和分裂,促进植物生长发育。然而,高浓度时,它表现出生长抑制作用,包括生长和阻止茎和根的生长。后一种效应形成了合成生长素被开发为农业除草剂和生物调节剂的基础。 | |||
TMM2618 |
Gibberllin A7
Gibberellin A7,Gibberllin 7,赤霉素GA7 |
Others | Others |
Gibberllin A7 (Gibberllin 7) 是重要的植物生长激素,可促进植物细胞生长和伸长。它可促进茎和根的快速生长,诱导有丝分裂并启动(打破休眠)并提高种子发芽率。它还参与诸如作为向地力、张力和花卉展示。Gibberellin A3(G1025, G7645) 和 A4 (G7276) 可用作植物生长培养基如 Murashige 和 Skoog 培养基的补充剂。 A3 和 A4 或 Gebberellins 组合的具体作用应在具体的植物应用中确定。 | |||
T38141 |
Glycerophospholipids, cephalins
Phosphatidylethanolamines (egg) |
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Glycerophospholipids, cephalins (Phosphatidylethanolamines (egg)) 是一种从鸡蛋中分离出来的磷脂酰乙醇胺的混合物,在 sn-1和 sn-2位置有各种脂肪酰基。Glycerophospholipids, cephalins 完全水解可得到1mol 的甘油、磷酸、乙醇胺和2mol 的脂肪酸。Phosphatidylethanolamines 在膜融合和细胞分裂过程中收缩环的拆卸中起作用,可调节膜的弯曲度。Phosphatidylethanolamines 能够在没有任何蛋白质或核酸的帮助下传播传染性朊病毒。Phosphatidylethanolamines 在细菌膜中的主要作用之一是分散由阴离子膜磷脂引起的负电荷。 | |||
T4454 |
Traumatic Acid
Dodec-2-Enedioic Acid,2E-Dodecenedioic Acid,愈伤酸,Trans-2-Dodecenedioic Acid |
Antioxidant | oxidation-reduction |
Traumatic Acid (Dodec-2-Enedioic Acid) 是一种单不饱和二元羧酸,从菜豆中分离得到。它可减少膜磷脂的过氧化,并表现出抗氧化和对胶原生物合成的刺激作用。它可用于许多与胶原蛋白生物合成障碍和氧化应激有关的皮肤疾病的研究。 | |||
T75520 | Aplyronine A | ||
Aplyronine A是具有特异性肌动蛋白解聚活性、抗肿瘤及促凋亡功能的化合物,适用于癌症、肌肉收缩、细胞运动和细胞分裂等研究领域。 | |||
TN4890 |
Rabdosin B
|
Others | Others |
Rabdosin B shows cytotoxic activity against three human tumour HepG2, GLC-82 and HL-60 cell lines, it induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner. Rabdosin B at higher concentrations inhibits root growth by affecting | |||
TN4249 | Ilicol | Others | Others |
Pinocembrin and Ilicol inhibit root growth and show IC50 (root growth) values of 0.199, 14.68, 8.05, 7.69 mM, and 1.22, 2.90, 7.35, 8.07 mM, against P. miliaceum, A. sativa, L. sativa, and R. sativus, respectively. They reduce Allium cepa cell |