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Cat. No. | Product Name | Target | Signaling Pathways |
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T6116L |
Bleomycin hydrochloride
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Bleomycin hydrochloride is a potent antitumor antibiotic that functions as a DNA synthesis inhibitor and DNA damaging agent. | |||
T65016 | Bleomycin A2 | ||
Bleomycin A2,作为一种抗肿瘤抗生素,能促进DNA降解,同时也是一种天冬氨酸/天冬酰胺-β-羟化酶(AspH)的抑制剂,其IC50为1.47 μM。 | |||
T73606 |
Bleomycin B4
|
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Bleomycin B4 (Phleomycin F),一种具有抗肿瘤活性的抗生素,常用于癌症研究。 | |||
T71445 | Bleomycin Free Base | ||
Bleomycin Free Base is a complex of related glycopeptide antibiotics from Streptomyces verticillus consisting of bleomycin A2 and B2. It inhibits DNA metabolism and is used as an antineoplastic, especially for solid tumors. | |||
T74722 |
Demethyl bleomycin A2
|
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Demethyl bleomycin A2 是Bleomycin 的同源物。Demethyl bleomycin A2 的 DNA 裂解对5-Methylcytidine 不敏感。 | |||
T10110 |
3-CPs
3-Carbethoxypsoralen,3-Ethoxycarbonylpsoralen |
Antibiotic | Microbiology/Virology |
3-CPs (3-Carbethoxypsoralen) 是一种博来霉素诱导的小鼠肺纤维化血清型荚膜多糖,属于补骨脂,可干扰抗体介导的细菌杀伤作用。3-CPs 可延缓博来霉素诱导的小鼠肺纤维化,可用于研究气道炎和哮喘。 | |||
T30778 |
CCG-257081
MRTF/SRF-IN-1,CCG257081,CCG 257081 |
Rho; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
CCG-257081 (MRTF/SRF-IN-1) 是心肌素相关转录因子和血清反应因子 (MRTF/SRF) 的抑制剂,通过抑制 Rho/MRTF/SRF 通路来发挥作用。CCG-257081 已在多个小鼠模型中显示出预防博莱霉素诱导的纤维化的功效。CCG-257081 可用于预防癌症和纤维化的研究。 | |||
T36416 |
N1-Acetylspermine trihydrochloride
N1-Acetylspermine (hydrochloride) |
Others | Others |
N1-Acetylspermine trihydrochloride 是精胺的单乙酰化衍生物,精胺是一种内源性多胺。 N1-Acetylspermine trihydrochloride 可用于研究人体肉毒碱转运蛋白 SLC22A16 对抗癌多胺类似物博莱霉素 A5 的摄取。 | |||
T28177 |
NK3201
NK-3201,NK 3201 |
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NK3201, a specific chymase inhibitor, suppresses bleomycin-induced pulmonary fibrosis in hamsters. | |||
T73662 |
Peplomycin
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Peplomycin (Bleomycin PEP; Pepleomycin) 是Bleomycin 的类似物,具有很高的抗肿瘤作用和较少的肺毒性。Peplomycin 可诱导多种皮肤异常,并诱导口腔鳞癌 SSCKN 细胞凋亡 (apoptosis),诱导肺纤维化。 | |||
T28788 |
SK-216
SK216.Plasminogen activator inhibitor-1 (PAI-1) inhibitor |
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SK-216 is a specific PAI-1 inhibitor. SK-216 reduced the extent of angiogenesis in the tumors and inhibited VEGF-induced migration and tube formation by human umbilical vein endothelial cells in vitro. SK-216 reduced the degree of bleomycin-induced pulmon | |||
T73721 |
Phleomycin D1
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Phleomycin D1 (PLM D1)为Bleomycin/Phleomycin家族内的一种糖肽类抗生素,作用机制是通过结合DNA并切割之,从而引发细胞死亡。 | |||
T79642 |
IV-275
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
IV-275为BRG1与BRM溴域的抑制剂,能够增强Temozolomide和Bleomycin所诱导的DNA损害。此外,IV-275可抑制GBM(Glioblastoma multiforme)细胞的侵袭性,并增强Temozolomide所诱导的细胞凋亡。 | |||
T82313 |
GK718
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HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
GK718为一HDAC1/3特异性抑制剂,IC50值分别为259 nM和139 nM。该化合物能提升细胞内乙酰化组蛋白H3含量,并能够抑制Bleomycin所诱导的小鼠肺纤维化现象。 | |||
T78202 | IV-255 | Epigenetic Reader Domain | Chromatin/Epigenetic |
IV-255为BRG1溴域的选择性小分子抑制剂,能增强Temozolomide及Bleomycin诱导的DNA损伤。此外,IV-255抑制GBM细胞侵袭,并强化Temozolomide诱导的细胞死亡与细胞凋亡活性。 | |||
T61612 |
ATX inhibitor 15
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ATX inhibitor 15 (compound 30) is an indole-based carbamate derivative with a strong inhibitory effect on autotaxin (ATX), demonstrated by an IC50 of 2.17 nM. Additionally, ATX inhibitor 15 effectively inhibits ATX activity in vivo and suppresses the expression of pro-fibrotic genes. Furthermore, ATX inhibitor 15 exhibits protective effects in lung fibrosis induced by Bleomycin in mice [1]. | |||
T74632 | TP0556351 | MMP | Proteases/Proteasome |
TP0556351是一种高效且选择性地抑制基质金属蛋白酶2 (MMP2) 的化合物,其IC50值为0.2 nM。在Bleomycin诱导的肺纤维化小鼠模型中,该化合物能显著减少肺部胶原蛋白的含量,适用于特发性肺纤维化(IPF)的研究。 | |||
T36338 |
AAF-CMK (trifluoroacetate salt)
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Tripeptidyl peptidase II (TPPII) is a serine peptidase of the subtilisin-type which removes tripeptides from the free NH2 terminus of oligopeptides. AAF-CMK is an irreversible inhibitor of TPPII commonly used at 10-100 μM. It does not significantly interfere with the chymotrypsin-like activity of the proteasome. AAF-CMK also inhibits bleomycin hydrolase and puromycin-sensitive aminopeptidase when used at 50 μM. | |||
T36385 |
Ansatrienin A
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Ansatrienin A is an ansamycin antibiotic and antifungal agent first isolated from S. collinus and S. rishiriensis. In fetal rat long bones, it is an inhibitor of parathyroid hormone-induced calcium release (IC50 = 64 nM), which is a measure of bone resorption, and pp60c-srcM kinase (IC50 = 100 nM). It also inhibits TNF-α-induced expression of intercellular adhesion molecule-1 (ICAM-1; IC50 = 570 nM). Early in vitro studies showed that ansatrienin A potentiates the chemotherapeutic action of 5-fl... | |||
T82314 |
GK444
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HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
GK444(Compound 15a),一种针对HDAC1/2的抑制剂,IC50分别为HDAC1和HDAC2的100 nM与92 nM。其对Caco-2细胞的IC50为4.1μM,并能下调原代正常人肺成纤维细胞中TGF-β1刺激的COL1A1 mRNA水平。此外,GK444还能抑制博来霉素诱发的小鼠肺纤维化。 | |||
T36650 |
Ansatrienin B
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Ansatrienin B is an ansamycin antibiotic and antifungal agent first isolated from S. collinus and S. rishiriensis., In fetal rat long bones, it is an inhibitor of parathyroid hormone-induced calcium release (IC50 = 21 nM), which is a measure of bone resorption, and pp60c-src kinase (IC50 = 50 nM). It is an inhibitor of translation at the protein synthesis stage by specific inhibition of L-leucine incorporation (IC50 = 58 nM in A549 cells). It also inhibits TNF-α-induced expression of intercellul... | |||
T36659 |
Boromycin
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Boromycin is a boron-containing macrolide antibiotic that has been found in Streptomyces. Boromycin inhibits growth of B. subtilis (MIC = 0.05 μg/ml) and induces efflux of potassium ions from B. subtilis without affecting Na+/K+-ATPase activity. It decreases the synthesis of protein, RNA, and DNA in B. subtilis when used at a concentration of 0.05 μg/ml. It inhibits the growth of B. halodurans (MIC = 10 ng/ml) and inhibits the futalosine pathway of menaquinone synthesis in B. halodurans. Boromyc... | |||
T65994 |
(6S)-N-Benzyl-6-(4-hydroxybenzyl)-8-(naphthalen-1-ylmethyl)-4,7-dioxohexahydro-2H-pyrazino[1,2-a]pyrimidine-1(6H)-carboxamide
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Wnt signaling is required for direct multiple biological processes and also plays key roles in the pathogenesis of various diseases. Cyclic AMP response element-binding protein (CREB) is a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds as a homodimer to the cAMP-responsive element, an octameric palindrome. The protein is phosphorylated by several protein kinases, and induces transcription of genes in response to hormonal stimulation... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T6116 |
Bleomycin Sulfate
Blenoxane,硫酸博来霉素,硫酸博莱霉素,NSC125066 |
DNA/RNA Synthesis; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Bleomycin Sulfate (Blenoxane) 是一种糖肽抗生素,一种 DNA 合成抑制剂。Bleomycin Sulfate 可以引起 DNA 链断裂而不引起 RNA 链断裂。Bleomycin Sulfate 具有抗肿瘤活性。 | |||
T75508 |
Bleomycin A5
|
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Bleomycin A5 (Pingyangmycin),一种具有口服活性的糖肽类抗生素,既是抗肿瘤剂、细胞凋亡诱导剂,又是细菌代谢产物。 | |||
T4953 |
Neotuberostemonine
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NOS | Immunology/Inflammation |
Neotuberostemonine 是一种结核分枝杆菌根中主要的止咳生物碱,能够阻碍巨噬细胞的募集和活化,从而减轻博来霉素 (Bleomycin) 诱导的肺纤维化。 | |||
T6S0105 |
Peiminine
贝母素乙,Zhebeinone,Fritillarine,Raddeanine,Verticinone |
Others; Autophagy | Autophagy; Others |
Peiminine (Raddeanine) 是浙贝母中的一种生物碱,具有抗炎症活性。 | |||
T21498 |
Phleomycin
|
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Phleomycin 是在链霉菌中发现的,引起 DNA 切割的抗癌糖肽抗生素之一。 它类似于博来霉素,它结合并插入 DNA 以破坏双螺旋的完整性。 | |||
T2S0690 |
Ecliptasaponin A
早莲苷 A,旱莲苷A,Echinocystic acid-3-o-glucoside |
Others | Others |
Ecliptasaponin A (Echinocystic acid-3-o-glucoside) 是一种墨旱莲 (Eclipta prostrate) 中分离得到的五环三萜皂苷。其中墨旱莲是一种具有多效作用的滋补草药,如抗炎、保肝、抗氧化和免疫调节。 | |||
T2762 |
Kasugamycin hydrochloride
Kasumin,盐酸春雷霉素 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Kasugamycin hydrochloride (Kasumin) 是一种能结合 30s 和 70s 核糖体,但不能结合 50s 亚基的抗生素。它模拟 mRNA 核苷酸以破坏 tRNA 结合并抑制经典翻译起始。 | |||
TN3469 |
Aucuparin
2,6-dimethoxy-4-phenylphenol |
NADPH-oxidase | Immunology/Inflammation |
Aucuparin (2,6-dimethoxy-4-phenylphenol) 是一种植物抗菌素,具有抗炎活性。 在博来霉素 (BLM) 诱导的肺纤维化小鼠模型中,Aucuparin 抑制肺纤维化。 在经ABTS 和FRAP 测定显示出明显的清除活性。 Aucuparin 对fmlp 诱导的人中性粒细胞产生超氧化物具有明显的抑制作用,其IC50为17.0μM。 | |||
T3795 |
Corilagin
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Apoptosis; TLR; Reverse Transcriptase; Antibacterial; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology |
Corilagin 是一种鞣酸,有抑制 RNA 肿瘤病毒逆转录酶的活性。它抑制金黄色葡萄球菌的生长,MIC 为 25 μg/mL。它有抗肿瘤活性,可用于肝癌和卵巢癌。 | |||
TN5879 |
Edgeworin
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Edgeworin is a DNA polymerase beta (pol beta) inhibitor, it inhibits both the lyase and polymerase activities of DNA polymerase beta; it can potentiate the inhibitory action of the anticancer drug bleomycin in cultured A549 cells via an inhibition of DNA | |||
T36961 |
Malformin C
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Malformin C is a natural fungus-derived bicyclic pentapeptide that has antibacterial properties, particularly against species of Bacillus. Malformin C potently blocks the ability of bleomycin to induce G2 arrest in human T-cell leukemia-derived Jurkat cells (IC50 = 0.9 nM). It less potently abrogates colchicine-induced M phase arrest in Jurkat cells (IC50 = 24 nM). Malformin C inhibits cell growth dose-dependently in Colon 38 and HCT 115 cancer cells (IC50s = 0.27 and 0.18 μM, respectively) but ... |