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描述 | Auristatin F, recognized for its significant cytotoxicity in antibody-linked therapies and as an MMAF analogue, acts as a potent disruptor of microtubules and a vascular damage agent (VDA). It halts cellular division by blocking the assembly of tubulin. Auristatin F is applicable in the creation of ADCs[1].[2]. |
体内研究 | In male Sprague-Dawley rats, Auristatin F administered intravenously at 5 mg/kg, achieves a peak concentration (Cmax) of 8276.76 ng/mL, with a last area under the curve (AUClast) of 65661.30 min*ng/mL and a clearance rate (CL) of 77.33 mL/min/kg, surpassing the rat's hepatic blood flow rate[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.34mL 0.27mL 0.13mL |
6.70mL 1.34mL 0.67mL |
13.41mL 2.68mL 1.34mL |
CAS号 | 163768-50-1 |
分子式 | C40H67N5O8 |
分子量 | 745.99 |
SMILES Code | CC(C)[C@H](N(C)C)C(N[C@H](C(N([C@@H]([C@@H](C)CC)[C@@H](CC(N1CCC[C@@]1([H])[C@H](OC)[C@@H](C)C(N[C@H](C(O)=O)CC2=CC=CC=C2)=O)=O)OC)C)=O)C(C)C)=O |
MDL No. | MFCD25976745 |
别名 | |
运输 | 蓝冰 |
InChI Key | LGNCNVVZCUVPOT-FUVGGWJZSA-N |
Pubchem ID | 67472795 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
DMSO: 190 mg/mL(254.7 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |