Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.

显示细胞生长制和细胞毒活性。EGFR激制剂。有抗血管生成活性。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC制剂。诱导凋亡。

Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.

TAN-420E曾有抗肿瘤活性，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。

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。有血管生成活性。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

雌激素。选择性PKC抑制剂。诱导凋亡。

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）基因进行的系列研究。

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。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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，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。

Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.

显示细生长抑制和细性。EGFR抑制剂。有抗血管生成性。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌素。选择性PKC抑制剂。诱导凋亡。

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能包含JAK-STAT信号通路在内的多种促细有丝分裂信号通路。

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（UCK，EC 2.7.1.48）基因进行的一系列研究。

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。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC抑制。诱导凋亡。

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，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。

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酶抑制剂。有管生成活性。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

雌素。选择性PKC抑制剂。诱导凋亡。

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酶（UCK，EC 2.7.1.48）基因进行的一系列研究。

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。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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JAK-STAT号通路在内的多种促细胞有丝分裂号通路。

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。

Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.

显示细胞长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血活性。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC抑制剂。诱导凋亡。

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。

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。

Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.

抗雌激素。选择性PKC抑制。诱导凋亡。

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，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。