Topotecan
Price | $1 |
Package | 1KG |
Min. Order: | 1G |
Supply Ability: | 100KG |
Update Time: | 2019-07-06 |
Product Details
Product Name: Topotecan | CAS No.: 123948-87-8 |
Min. Order: 1G | Purity: 98% |
Supply Ability: 100KG | Release date: 2019/07/06 |
AD68
Topotecan Basic information |
Camptothecin anticancer drugs Uses Production methods |
Product Name: | Topotecan |
Synonyms: | hycamptamine;HYDROGEN CHLORIDE, BUTANOL REAGENT;HYDROGEN CHLORIDE GAS;HYDROGEN CHLORIDE, METHANOL REAGENT;HYDROGEN CHLORIDE, METHANOL REAGENT 10;HYDROGEN CHLORIDE, METHANOL REAGENT 5;HYDROCHLORIC ACID,1.1M;HYDROCHLORIC ACID, 1N |
CAS: | 123948-87-8 |
MF: | C23H23N3O5 |
MW: | 421.45 |
EINECS: | 231-595-7 |
Product Categories: | APIs;API |
Mol File: | 123948-87-8.mol |
Topotecan Chemical Properties |
Melting point | −114 °C(lit.) |
Boiling point | >100 °C(lit.) |
density | 1.2 g/mL at 25 °C(lit.) |
vapor density | 1.3 (vs air) |
vapor pressure | 613 psi ( 21.1 °C) |
Fp | 12 °C |
storage temp. | 2-8°C |
solubility | H2O: soluble |
form | liquid |
color | yellow |
CAS DataBase Reference | 123948-87-8(CAS DataBase Reference) |
Safety Information |
Hazard Codes | T,C,F,Xi |
Risk Statements | 36/37/38-67-35-20-11-34-48-46-36 |
Safety Statements | 26-45-36/37/39-37/39-36-22-24/25-16-7 |
RIDADR | UN 3286 3/PG 2 |
WGK Germany | 2 |
RTECS | MW4025000 |
F | 3 |
HazardClass | 8 |
PackingGroup | II |
Topotecan Usage And Synthesis |
Camptothecin anticancer drugs | Camptothecin anticancer drugs are alkaloids or derivatives of them after the structure transformation raised from deciduous plant Davidia involucrata Camptotheca acuminate seed or root bark. Clinical application of them mainly includes camptothecin,hydroxycamptothecin, topotecan and irinotecan. Topotecan is a water-soluble semi-synthetic derivative of camptothecin,it is a topoisomerase I inhibitor, inhibiting DNA single strand DNA scission reconnect to damage DNA, its cytotoxicity occurs in cancer cell division S phase, it is an s phase cell cycle specific drug . In vivo it is a two-compartment model,it can be quickly distributed to the liver, kidneys and other parts , of a single intravenous infusion 1.5mg/m2 every 30 minutes , t1/2αis 4.1 to 8.1 minutes, plasma protein binding rate is 6.6%~21.3%,it can go into the cerebrospinal fluid. Most of it is excreted by the kidneys, a small part of it is excreted by the bile, within 12 hours, 90% of it is excreted.Clearance rate of renal dysfunction decreases.it is clinically used for the treatment of small cell lung cancer (SCLC), and advanced ovarian cancer, because it can penetrate the blood-brain barrier ,it has a certain effect on the central nervous system cancer and brain metastases. Usage: every single drug dose 1.2mg/m2 intravenous infusion once a day, once every 5 days, 21 days is 1 cycle, there is the need to reduce the dose when in combination with other anticancer drugs. The main adverse events are hematologic toxicity, white blood cells, platelets and hemoglobin decrease; non-hematologic toxicity adverse events are loss of appetite, nausea, vomiting, hair loss, stomatitis, diarrhea, headache, fever, constipation, transient elevated transaminase; occasionally breathing difficulties, hematuria, andelectrocardiogram abnormalities. Severe bone marrow suppression are hanged. Monitor the blood and adjust the dose in accordance with changes in blood during the treatment , if necessary, granulocyte colony stimulating factor (G-CSF), and transfusion of blood components may be given . The above information is edited by the chemicalbook of Tian Ye. |
Uses | Anti-cancer drugs.It can be used alone for the treatment of initially or continuously ineffective chemotherapy metastatic ovarian cancer. |
Production methods | Compound (I) with 37% formaldehyde and 40% dimethylamine,after aminomethylation in acetic acid, produces the product. |
Chemical Properties | Off-white Cryst |
Uses | antineoplastic;DNA topoisomerase type 1 inhibitor |
Definition | ChEBI: A pyranoindolizinoquinoline used as an antineoplastic agent. It is a derivative of camptothecin and works by binding to the topoisomerase I-DNA complex and preventing religation of these 328 single strand breaks. |
Company Profile Introduction
Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals.
Mainly deals in the sales of:
Pharmaceutical intermediates
OLED intermediates:
Pharmaceutical intermediates;
OLED intermediates;
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- Since: 2014-12-17
- Address: No.967,15th Floor,Unit 7, Building 1, No.70 of DianChang Road, High-tech Development Zone, Zhengzho
INQUIRY
楊俊青
sales@coreychem.com
sales@coreychem.com