CasNo.123948-87-8,Topotecan 123948-87-8,(123948-87-8) Suppliers

100 Kilogram	Negotiable

Min.Order :100 Kilogram
Purity: 99%
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Keywords

RARECHEM AH PB 0251 123948-87-8 C23H23N3O5

Quick Details

Appearance:powder
Application:123948-87-8
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

Superiority:

Topotecan Basic information

Camptothecin anticancer drugs Application 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

mp	−114 °C(lit.)
bp	>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
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

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

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.
Application	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
Usage	antineoplastic;DNA topoisomerase type 1 inhibitor

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