Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行
一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件
观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择PKC抑制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒。EGFR激酶抑制剂。有抗血管生成
。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤,
氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词
分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌素。选择性PKC
制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞制和细胞毒活性。EGFR
制剂。有抗血管
成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动
成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除,
具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互
网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激抑制剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要对人类尿苷胞苷激
(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧Herbimycin A,
者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌素。选择性PKC抑制剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显生长抑制和
毒活性。EGFR
酶抑制剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能活包含JAK-STAT信号通路在内的多种促
有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷苷
酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑剂。诱导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示胞生长抑
胞毒活性。EGFR激酶抑
剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌素。选择性PKC抑制剂。诱导凋
。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
细胞生长抑制和细胞毒活性。EGFR
抑制剂。有抗血管生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。