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.
显示细胞长抑制和细胞毒
性。EGFR激酶抑制剂。有抗血管
性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
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
,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.
显示细胞生长抑制和细胞毒性。EGFR
抑制剂。有抗血管生成
性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
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。
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.
胞生长抑制和
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
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。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
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
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曾报道有活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定
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(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。
导凋亡。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑和细胞毒活性。EGFR激
抑
。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,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(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,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性。EGFR
抑制剂。有抗血管生成
性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
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NOK
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。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
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
生成活性。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定
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(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。