Synonym
T-2513; 288247-87-0; 20Y8Q506KT; T 2513; UNII-20Y8Q506KT; T2513
IUPAC/Chemical Name
(S)-9-(3-aminopropoxy)-4,11-diethyl-4-hydroxy-1,12-dihydro-14H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H)-dione
InChi Key
XZLHHOGJQUVONU-VWLOTQADSA-N
InChi Code
InChI=1S/C25H27N3O5/c1-3-15-16-10-14(32-9-5-8-26)6-7-20(16)27-22-17(15)12-28-21(22)11-19-18(23(28)29)13-33-24(30)25(19,31)4-2/h6-7,10-11,31H,3-5,8-9,12-13,26H2,1-2H3/t25-/m0/s1
SMILES Code
CCC1=C2CN3C(=CC4=C(COC(=O)[C@]4(O)CC)C3=O)C2=NC5=CC=C(OCCCN)C=C15
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
449.51
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Harada M, Imai J, Okuno S, Suzuki T. Macrophage-mediated activation of
camptothecin analogue T-2513-carboxymethyl dextran conjugate (T-0128): possible
cellular mechanism for antitumor activity. J Control Release. 2000 Dec
3;69(3):389-97. doi: 10.1016/s0168-3659(00)00320-5. PMID: 11102679.
2: Fujita F, Koike M, Fujita M, Sakamoto Y, Okuno S, Kawaguchi T, Yano S, Yano
T, Kiuchi S, Fujiwara T, Kudoh S, Kakushima M. MEN4901/T-0128, a new
camptothecin derivative-carboxymethyldextran conjugate, has potent antitumor
activities in a panel of human tumor xenografts in nude mice. Clin Cancer Res.
2005 Feb 15;11(4):1650-7. doi: 10.1158/1078-0432.CCR-04-1756. PMID: 15746070.
3: Ma H, Li X, Yang Z, Okuno S, Kawaguchi T, Yagi S, Bouvet M, Hoffman RM. High
antimetastatic efficacy of MEN4901/T-0128, a novel camptothecin
carboxymethyldextran conjugate. J Surg Res. 2011 Dec;171(2):684-90. doi:
10.1016/j.jss.2010.05.066. Epub 2010 Jun 25. PMID: 20851421; PMCID: PMC3008337.
4: Harada M, Sakakibara H, Yano T, Suzuki T, Okuno S. Determinants for the drug
release from T-0128, camptothecin analogue-carboxymethyl dextran conjugate. J
Control Release. 2000 Dec 3;69(3):399-412. doi: 10.1016/s0168-3659(00)00321-7.
PMID: 11102680.