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Search Results for " tetrandrine "

3

抑制剂 & 化合物

5

天然产物

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Cat. No. Product Name Target Signaling Pathways
T26911 Bromotetrandrine

5-Bromotetrandrine,W-198,BrTet,W 198,W198

Bromotetrandrine is an P-glycoprotein inhibitor, which were developed and coadministered with chemotherapeutic drugs to overcome the effect of efflux pumps thus enhancing the chemosensitivity of therapeutics.
T67948 OY-101

OY-101为口服生效的特异性P-glycoprotein(P-gp)抑制剂。该化合物可增强耐药性肿瘤的敏感性,并有效逆转多药耐药现象。相较于Tetrandrine,OY-101在水溶性、细胞毒性以及逆转活性方面均表现出改进。
T36805 TPC2-A1-N

TPC2-A1-N

TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2 through independent binding sites. TPC2-A1-N has inverse effects on key lysosomal activities and increases the pH in the lysosomal lumen in a TPC2-dependent manner[1].

化合物

Bromotetrandrine
Cat.No: T26911
Synonym: 5-Bromotetrandrine,W-198,BrTet,W 198,W198
Target:
OY-101
Cat.No: T67948
Synonym:
Target:
TPC2-A1-N
Cat.No: T36805
Synonym: TPC2-A1-N
Target:
Cat. No. Product Name Target Signaling Pathways
T2996 Tetrandrine

NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素

Potassium Channel; Calcium Channel Membrane transporter/Ion channel; Metabolism
Tetrandrine (Sinomenine A) 是来自粉防己的一种双苯基异喹啉生物碱,可抑制电压门控钙离子通道 (ICa) 和 Ca2+激活的钾离子通道。
T2809 (R)-Fangchinoline

防己醇灵,Thaligine,(+)-Thalrugosine,Demethyl tetrandrine

FAK; Antibacterial; Antibiotic Angiogenesis; Cytoskeletal Signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors
(R)-Fangchinoline ((+)-Thalrugosine) 是一种来自Stephania 属的生物碱,具有抗菌和降血压活性。它可用作中药,可用于发烧,腹泻,消化不良和泌尿疾病的研究。
T3122 Fangchinoline

Tetrandrine B,防己诺林碱,(+)-Limacine,Hanfangichin B,防己醇灵,(+)-Fangchinoline

Apoptosis; FAK; HIV Protease; Autophagy Angiogenesis; Apoptosis; Autophagy; Cytoskeletal Signaling; Microbiology/Virology; Proteases/Proteasome; Tyrosine Kinase/Adaptors
Fangchinoline (Tetrandrine B) 是从Stephaniatetrandra 中分离出来的,一种具有广泛生物学活性的天然产物。它是新型HIV-1抑制剂,通过损害 gp160 蛋白水解过程来抑制 HIV-1 复制。它靶向Focal adhesion kinase (FAK)并抑制肿瘤细胞中 FAK 介导的的信号传导途径。
TN4335 Isotetrandrine N-2'-oxide

Others Others
Isotetrandrine N-2'-oxide 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 TN4335,CAS号为 70191-83-2。
TN1806 Isotetrandrine

IL Receptor; NF-κB; MAPK Immunology/Inflammation; MAPK; NF-κB
Isotetrandrine is a small molecule inhibitor, on various aspects of LPS-induced inflammation in vitro and in vivo. It dose-dependently suppresses the severity of LPS-induced ALI by inactivation of MAPK and NF-κB, which may involve the inhibition of tissue

天然产物

Tetrandrine
Cat.No: T2996
Synonym: NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素
Target: Potassium Channel, Calcium Channel
(R)-Fangchinoline
Cat.No: T2809
Synonym: 防己醇灵,Thaligine,(+)-Thalrugosine,Demethyl tetrandrine
Target: FAK, Antibacterial, Antibiotic
Fangchinoline
Cat.No: T3122
Synonym: Tetrandrine B,防己诺林碱,(+)-Limacine,Hanfangichin B,防己醇灵,(+)-Fangchinoline
Target: Apoptosis, FAK, HIV Protease, Autophagy
Isotetrandrine N-2'-oxide
Cat.No: TN4335
Synonym:
Target: Others
Isotetrandrine
Cat.No: TN1806
Synonym:
Target: IL Receptor, NF-κB, MAPK
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