Cell Cycle/Checkpoint
Cell Cycle/Checkpoint(细胞周期/检查点)
Cell Cycle
Cells undergo a complex cycle of growth and division that is referred to as the cell cycle. The cell cycle consists of four phases, G1 (GAP 1), S (synthesis), G2 (GAP 2) and M (mitosis). DNA replication occurs during S phase. When cells stop dividing temporarily or indefinitely, they enter a quiescent state called G0. read more
- ATM/ATR(29)
- Aurora Kinase(58)
- Cdc42(4)
- Cdc7(3)
- Chk(14)
- c-Myc(27)
- CRM1(8)
- Cyclin-Dependent Kinases(77)
- E1 enzyme(1)
- G-quadruplex(12)
- Haspin(6)
- HMTase(1)
- Kinesin(27)
- Ksp(4)
- Microtubule/Tubulin(257)
- Mps1(15)
- Mitotic(7)
- RAD51(13)
- ROCK(74)
- Rho(13)
- PERK(11)
- PLK(43)
- PTEN(6)
- Wee1(9)
- PAK(25)
- Arp2/3 Complex(8)
- Dynamin(14)
- ECM & Adhesion Molecules(54)
- Cytoskeleton & Motor Proteins(65)
- Endomembrane System & Vesicular Trafficking(36)
- G1(51)
- Genotoxic Stress(23)
- G2/M(40)
- G2/S(17)
- Inositol Phosphates(67)
- Proteolysis(183)
- Cellular Chaperones(14)
- Cyclin G-associated Kinase (GAK)(1)
- MARK(3)
- NEKs(1)
Cell Cycle/Checkpoint 相关产品(1379)
- GC33269Valecobulin (CKD-516)CAS: 1188371-47-2纯度: >98.00%
Valecobulin (CKD-516) (CKD516) 是 (S516) 的缬氨酸前药和血管破坏剂 (VDA)。 Valecobulin (CKD-516) 是一种有效的 β-tubulin 聚合抑制剂,对小鼠和人类实体瘤具有显着的抗肿瘤活性。
- GC33291Tubulin inhibitor 1CAS: 2237054-53-2纯度: >99.50%
Tubulininhibitor1是tubulin抑制剂,靶作用于秋水仙素结合位点,抑制微管蛋白聚集。Tubulininhibitor1具有抗肿瘤活性,能够导致细胞G2/M期有丝分裂停滞,诱导细胞凋亡。
- GC33310Rho-Kinase-IN-1CAS: 1035094-83-7纯度: >99.50%
Rho-Kinase-IN-1是一个rho激酶抑制剂,来自专利US20090325960A1,化合物1.008。
- GC33362Amuvatinib hydrochloride (MP470 hydrochloride)CAS: 1055986-67-8
A multi-targeted RTK inhibitor
- GC33370Amphethinile (Amphetinile)CAS: 91531-98-5
Amphetinile (Amphetinile) 是一种抗微管蛋白剂。 Amphetinile (Amphetinile) 与微管蛋白结合的亲和常数 (Ka) 为 1.3 μM。
- GC33379Aurora B inhibitor 1CAS: 937276-52-3
AuroraBinhibitor1是一种AuroraB(Aurora-1)抑制剂,Ki值<0.010uM。详细信息请参考专利文献WO2007059299A1中的化合物1-3。
- GC33901Pentanoic acidCAS: 109-52-4纯度: >99.00%
Pentanoicacid是一种短链脂肪酸,是细菌代谢产物,与过敏性皮肤病有关系。Pentanoicacid能够激活ROCK信号通路。
- GC34022Ombrabulin hydrochloride (AVE8062)CAS: 253426-24-3纯度: >99.50%
A tubulin polymerization inhibitor and tumor vascular disrupting agent
- GC34068McMMAF (Maleimidocaproyl monomethylauristatin F)CAS: 863971-19-1纯度: >99.50%
McMMAF (Maleimidocaproyl monomethylauristatin F) 是一种保护基团缀合的 MMAF。 MMAF 是一种有效的微管蛋白聚合抑制剂。
- GC34073Empesertib (BAY 1161909)CAS: 1443763-60-7纯度: >98.00%
Empesertib (BAY1161909, Mps1-IN-5), a derivative of triazolopyridine, is an orally bioavailable, selective inhibitor of the serine/threonine monopolar spindle 1 (Mps1) kinase with IC50 of <1 nM. Empesertib has potential antineoplastic activity.
- GC34135Taltobulin trifluoroacetate (HTI-286 trifluoroacetate)CAS: 228266-41-9纯度: >99.50%
An inhibitor of microtubule polymerization
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC33269 | Valecobulin (CKD-516) | 1188371-47-2 | >98.00% | |
Valecobulin (CKD-516) (CKD516) 是 (S516) 的缬氨酸前药和血管破坏剂 (VDA)。 Valecobulin (CKD-516) 是一种有效的 β-tubulin 聚合抑制剂,对小鼠和人类实体瘤具有显着的抗肿瘤活性。 | ||||
| GC33291 | Tubulin inhibitor 1 | 2237054-53-2 | >99.50% | |
Tubulininhibitor1是tubulin抑制剂,靶作用于秋水仙素结合位点,抑制微管蛋白聚集。Tubulininhibitor1具有抗肿瘤活性,能够导致细胞G2/M期有丝分裂停滞,诱导细胞凋亡。 | ||||
| GC33300 | CCB02 | 2100864-57-9 | >99.50% | |
CCB02是一种选择性的CPAP-tubulin相互作用抑制剂,能够与tubulin结合,竞争β-tubulin的CPAP结合位点,IC50值为689nM,具有高效抗肿瘤活性。CCB02对其他的蛋白没有抑制作用,包括与细胞周期、中心体相关蛋白,同时对AuroraA,Plk1,Plk2,CDK2和CHK1的磷酸化状态无作用。 | ||||
| GC33310 | Rho-Kinase-IN-1 | 1035094-83-7 | >99.50% | |
Rho-Kinase-IN-1是一个rho激酶抑制剂,来自专利US20090325960A1,化合物1.008。 | ||||
| GC33362 | Amuvatinib hydrochloride (MP470 hydrochloride) | 1055986-67-8 | - | |
A multi-targeted RTK inhibitor | ||||
| GC33370 | Amphethinile (Amphetinile) | 91531-98-5 | - | |
Amphetinile (Amphetinile) 是一种抗微管蛋白剂。 Amphetinile (Amphetinile) 与微管蛋白结合的亲和常数 (Ka) 为 1.3 μM。 | ||||
| GC33377 | KSI-3716 | 1151813-61-4 | >98.50% | |
KSI-3716是c-Myc的抑制剂。 | ||||
| GC33379 | Aurora B inhibitor 1 | 937276-52-3 | - | |
AuroraBinhibitor1是一种AuroraB(Aurora-1)抑制剂,Ki值<0.010uM。详细信息请参考专利文献WO2007059299A1中的化合物1-3。 | ||||
| GC33404 | KU 59403 | 845932-30-1 | >98.50% | |
KU59403是ATM的一个有效抑制剂,其IC50值为3nM。 | ||||
| GC33420 | BAY-1895344 | 1876467-74-1 | >99.50% | |
An ATR inhibitor | ||||
| GC33421 | PAK-IN-1 | 1394121-05-1 | >99.00% | |
A group 2 PAK inhibitor | ||||
| GC33901 | Pentanoic acid | 109-52-4 | >99.00% | |
Pentanoicacid是一种短链脂肪酸,是细菌代谢产物,与过敏性皮肤病有关系。Pentanoicacid能够激活ROCK信号通路。 | ||||
| GC34022 | Ombrabulin hydrochloride (AVE8062) | 253426-24-3 | >99.50% | |
A tubulin polymerization inhibitor and tumor vascular disrupting agent | ||||
| GC34068 | McMMAF (Maleimidocaproyl monomethylauristatin F) | 863971-19-1 | >99.50% | |
McMMAF (Maleimidocaproyl monomethylauristatin F) 是一种保护基团缀合的 MMAF。 MMAF 是一种有效的微管蛋白聚合抑制剂。 | ||||
| GC34073 | Empesertib (BAY 1161909) | 1443763-60-7 | >98.00% | |
Empesertib (BAY1161909, Mps1-IN-5), a derivative of triazolopyridine, is an orally bioavailable, selective inhibitor of the serine/threonine monopolar spindle 1 (Mps1) kinase with IC50 of <1 nM. Empesertib has potential antineoplastic activity. | ||||
| GC34094 | Mycro 3 | 944547-46-0 | >99.00% | |
Mycro 3 is a potent and selective inhibitor of c-Myc in whole cell assays. Mycro 3 also shows weak inhibitory activity against AP-1. | ||||
| GC34102 | BNC105 | 945771-74-4 | >98.50% | |
An inhibitor of tubulin polymerization | ||||
| GC34109 | Tirbanibulin Mesylate (KX2-391 (Mesylate)) | 1080645-95-9 | >99.50% | |
A Src kinase inhibitor | ||||
| GC34135 | Taltobulin trifluoroacetate (HTI-286 trifluoroacetate) | 228266-41-9 | >99.50% | |
An inhibitor of microtubule polymerization | ||||
| GC34159 | Ilorasertib (ABT-348) | 1227939-82-3 | - | |
A multi-kinase inhibitor | ||||
| GC34297 | PF-2771 | 2070009-55-9 | >99.50% | |
PF-2771是一种选择性的着丝粒蛋白E(CENP-E)抑制剂,IC50值为16.1nM,具有抗肿瘤活性。 | ||||
| GC34300 | AR-13324 analog mesylate | 2095432-73-6 | - | |
AR-13324类似物甲磺酸盐是AR-13324的类似物。 | ||||
| GC34303 | Taltobulin hydrochloride (HTI-286 hydrochloride) | - | - | |
An inhibitor of microtubule polymerization | ||||
| GC34374 | BAY-1895344 hydrochloride | - | - | |
An ATR inhibitor | ||||
