Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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L125518-5mg | 5mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $48.90 | |
L125518-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $68.90 | |
L125518-50mg | 50mg | In stock | $147.90 | |
L125518-250mg | 250mg | In stock | $506.90 | |
L125518-1g | 1g | In stock | $1,822.90 | |
L125518-5g | 5g | In stock | $8,201.90 |
Synonyms | LENVATINIB [MI] | UNII-EE083865G2 | AS-16203 | LEV | NSC800781 | NSC-800781 | DB09078 | AKOS021983298 | LENVATINIB [INN] | AKOS015838040 | BCP9000633 | DTXSID30182868 | 4-(3-Chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7-methoxy-6-quinolinecarboxamide |
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Specifications & Purity | Moligand™, ≥99% |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of fms related receptor tyrosine kinase 4;Inhibitor of kinase insert domain receptor |
Note | 5mg、10mg、100mg卖完停产,不再备货 |
Product Description | Lenvatinib (E7080) is a multi-target inhibitor, mostly for VEGFR2(KDR)/VEGFR3(Flt-4) with IC50 of 4 nM/5.2 nM, less potent against VEGFR1/Flt-1, ~10-fold more selective for VEGFR2/3 against FGFR1, PDGFRα/β. Phase 3. Lenvatinib is an orally active inhibitor of multiple receptor tyrosine kinases including VEGF, FGF and SCF receptors. |
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Pubchem Sid | 488196334 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488196334 |
IUPAC Name | 4-[3-chloro-4-(cyclopropylcarbamoylamino)phenoxy]-7-methoxyquinoline-6-carboxamide |
INCHI | InChI=1S/C21H19ClN4O4/c1-29-19-10-17-13(9-14(19)20(23)27)18(6-7-24-17)30-12-4-5-16(15(22)8-12)26-21(28)25-11-2-3-11/h4-11H,2-3H2,1H3,(H2,23,27)(H2,25,26,28) |
InChi Key | WOSKHXYHFSIKNG-UHFFFAOYSA-N |
Canonical SMILES | COC1=CC2=NC=CC(=C2C=C1C(=O)N)OC3=CC(=C(C=C3)NC(=O)NC4CC4)Cl |
Isomeric SMILES | COC1=CC2=NC=CC(=C2C=C1C(=O)N)OC3=CC(=C(C=C3)NC(=O)NC4CC4)Cl |
Alternate CAS | 417716-92-8 |
PubChem CID | 9823820 |
MeSH Entry Terms | 4-(3-chloro-4-(((cyclopropylamino)carbonyl)amino)phenoxy)-7-hydroxy-6-quinolinecarboxamide;4-(3-chloro-4-((cyclopropylaminocarbonyl)amino)phenoxy)-7-methoxy-6-quinolinecarboxamide;4-(3-chloro-4-(N'-cyclopropylureido)phenoxy)-7-methoxyquinoline-6-carboxami |
Molecular Weight | 426.85 |
PubChem CID | 9823820 |
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ChEMBL Ligand | CHEMBL1289601 |
Wikipedia | Lenvatinib |
CAS Registry No. | 417716-92-8 |
RCSB PDB Ligand | LEV |
PEP | lenvatinib |
Reactome Reaction | R-HSA-2077420, R-HSA-9669854, R-HSA-9669900, R-HSA-9674430, R-HSA-9674095, R-HSA-2077424 |
Reactome Drug | R-ALL-2023393 |
DrugCentral Ligand | 4942 |
PubChem SID | 488196334 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
D2219078 | Certificate of Analysis | Feb 21, 2024 | L125518 |
H2127404 | Certificate of Analysis | Jun 08, 2023 | L125518 |
H2127405 | Certificate of Analysis | Jun 08, 2023 | L125518 |
H2127406 | Certificate of Analysis | Jun 08, 2023 | L125518 |
H2127407 | Certificate of Analysis | Jun 08, 2023 | L125518 |
C2127090 | Certificate of Analysis | Jan 12, 2023 | L125518 |
B23081009 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308857 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308858 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308865 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308866 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308918 | Certificate of Analysis | Nov 17, 2022 | L125518 |
B2308919 | Certificate of Analysis | Nov 17, 2022 | L125518 |
H1623002 | Certificate of Analysis | May 09, 2022 | L125518 |
D2219077 | Certificate of Analysis | Mar 05, 2022 | L125518 |
D2219090 | Certificate of Analysis | Mar 05, 2022 | L125518 |
Solubility | DMSO 40 mg/mL (93.7 mM); Water <1 mg/mL (<1 mM); Ethanol <1 mg/mL (<1 mM) |
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1. Mengming Xia, Xueyi Song, Zebei Lu, Yu Wang, Quan Zhou, Peiwu Geng, Shuanghu Wang, Yunfang Zhou, Qingjun Wu, Aixia Han. (2023) Evaluation of the inhibitory effect of azoles on pharmacokinetics of lenvatinib in rats both in vivo and in vitro by UPLC-MS/MS. Thoracic Cancer, 14 (33): (3331-3341). [PMID:37771131] |
2. Jie Yao, Shuming Tang, Chenyan Shi, Yunzhi Lin, Lanlan Ge, Qinghua Chen, Baoru Ou, Dongyu Liu, Yuyang Miao, Qiujie Xie, Xudong Tang, Jia Fei, Guangyi Yang, Jun Tian, Xiaobin Zeng. (2023) Isoginkgetin, a potential CDK6 inhibitor, suppresses SLC2A1/GLUT1 enhancer activity to induce AMPK-ULK1-mediated cytotoxic autophagy in hepatocellular carcinoma. Autophagy, 19 (4): (1221-1238). [PMID:36048765] |
1. Musumeci F, Radi M, Brullo C, Schenone S. (2012) Vascular endothelial growth factor (VEGF) receptors: drugs and new inhibitors.. J Med Chem, 55 (24): (10797-822). [PMID:23098265] |
2. Kudo M, Finn RS, Qin S, Han KH, Ikeda K, Piscaglia F, Baron A, Park JW, Han G, Jassem J et al.. (2018) Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial.. Lancet, 391 (10126): (1163-1173). [PMID:29433850] |
3. Mengming Xia, Xueyi Song, Zebei Lu, Yu Wang, Quan Zhou, Peiwu Geng, Shuanghu Wang, Yunfang Zhou, Qingjun Wu, Aixia Han. (2023) Evaluation of the inhibitory effect of azoles on pharmacokinetics of lenvatinib in rats both in vivo and in vitro by UPLC-MS/MS. Thoracic Cancer, 14 (33): (3331-3341). [PMID:37771131] |
4. Jie Yao, Shuming Tang, Chenyan Shi, Yunzhi Lin, Lanlan Ge, Qinghua Chen, Baoru Ou, Dongyu Liu, Yuyang Miao, Qiujie Xie, Xudong Tang, Jia Fei, Guangyi Yang, Jun Tian, Xiaobin Zeng. (2023) Isoginkgetin, a potential CDK6 inhibitor, suppresses SLC2A1/GLUT1 enhancer activity to induce AMPK-ULK1-mediated cytotoxic autophagy in hepatocellular carcinoma. Autophagy, 19 (4): (1221-1238). [PMID:36048765] |