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Catalog Number | ACM19685100 |
CAS Number | 19685-10-0 |
Structure | ![]() |
Synonyms | (4S)-9-Methoxy-4α-ethyl-4β-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione |
Molecular Weight | 378.4 |
InChI | InChI=1S/C21H18N2O5/c1-3-21(26)15-8-17-18-12(6-11-7-13(27-2)4-5-16(11)22-18)9-23(17)19(24)14(15)10-28-20(21)25/h4-8,26H,3,9-10H2,1-2H3/t21-/m0/s1 |
InChI Key | KLFJSYOEEYWQMR-NRFANRHFSA-N |
Melting Point | 254-255 °C |
Purity | 95%+ |
Complexity | 790 |
Covalently-Bonded Unit Count | 1 |
Defined Atom Stereocenter Count | 1 |
Exact Mass | 378.12157168 |
Heavy Atom Count | 28 |
Hydrogen Bond Acceptor Count | 6 |
Hydrogen Bond Donor Count | 1 |
Isomeric SMILES | CC[C@@]1(C2=C(COC1=O)C(=O)N3CC4=C(C3=C2)N=C5C=CC(=CC5=C4)OC)O |
Monoisotopic Mass | 378.12157168 |
PhysicalState | Powder |
Rotatable Bond Count | 2 |
Topological Polar Surface Area | 89 Ų |
What is the molecular formula of 10-Methoxycamptothecin?
The molecular formula of 10-Methoxycamptothecin is C21H18N2O5.
What is the molecular weight of 10-Methoxycamptothecin?
The molecular weight of 10-Methoxycamptothecin is 378.38.
What is the primary usage of 10-Methoxycamptothecin?
10-Methoxycamptothecin is primarily used in the treatment of cancers.
What class of compound does 10-Methoxycamptothecin belong to?
10-Methoxycamptothecin belongs to the Camptothecin derivative class of compounds.
Why is 10-Methoxycamptothecin used in the treatment of hyperproliferative diseases?
10-Methoxycamptothecin is used in the treatment of hyperproliferative diseases due to its anti-cancer properties.
How is 10-Methoxycamptothecin typically administered for cancer treatment?
10-Methoxycamptothecin is typically administered through intravenous injection for cancer treatment.
What is the mechanism of action of 10-Methoxycamptothecin in treating cancers?
The mechanism of action of 10-Methoxycamptothecin in treating cancers involves inhibiting DNA topoisomerase I.
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