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Hydroxycarbamid

Hydroxyurea Struktur
127-07-1
CAS-Nr.
127-07-1
Bezeichnung:
Hydroxycarbamid
Englisch Name:
Hydroxyurea
Synonyma:
HYDROXYCARBAMIDE;hu;1-hydroxyurea;hydrea;N-HYDROXYUREA;DROXIA;Siklos;tetratogen: inhibits ribonucleoside diphosphate reductase;NHY;hidrix
CBNumber:
CB8249322
Summenformel:
CH4N2O2
Molgewicht:
76.05
MOL-Datei:
127-07-1.mol

Hydroxycarbamid Eigenschaften

Schmelzpunkt:
135-140 °C
Siedepunkt:
136.04°C (rough estimate)
Dichte
1.457±0.06 g/cm3(Predicted)
Brechungsindex
1.4840 (estimate)
storage temp. 
2-8°C
L?slichkeit
H2O: 50 mg/mL
Aggregatzustand
powder
pka
10.56±0.23(Predicted)
Farbe
white
Geruch (Odor)
odorless or almost odorless
Wasserl?slichkeit
soluble
Merck 
14,4848
BRN 
1741548
Stabilit?t:
Stable for 2 years as supplied from date of purchase. Solutions in water may be stored at -20°C for up to 3 months.
CAS Datenbank
127-07-1(CAS DataBase Reference)
IARC
3 (Vol. 76) 2000
EPA chemische Informationen
Hydroxyurea (127-07-1)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher T,Xn
R-S?tze: 46-63-61-40
S-S?tze: 53-36/37-45-36-22
RIDADR  2811
WGK Germany  3
RTECS-Nr. YT4900000
Hazard Note  Toxic
HazardClass  6.1
PackingGroup  III
HS Code  29242100
Giftige Stoffe Daten 127-07-1(Hazardous Substances Data)
Toxizit?t dog,LD50,intravenous,> 1gm/kg (1000mg/kg),Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 23, Pg. 682, 1992.
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H340 Kann genetische Defekte verursachen. Keimzellmutagenit?t Kategorie 1B Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" />
H361 Kann vermutlich die Fruchtbarkeit beeintr?chtigen oder das Kind im Mutterleib sch?digen. Reproduktionstoxizit?t Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
Sicherheit
P201 Vor Gebrauch besondere Anweisungen einholen.
P308+P313 BEI Exposition oder falls betroffen: ?rztlichen Rat einholen/?rztliche Hilfe hinzuziehen.

Hydroxycarbamid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R46:Kann vererbbare Sch?den verursachen.
R63:Kann das Kind im Mutterleib m?glicherweise sch?digen.
R61:Kann das Kind im Mutterleib sch?digen.
R40:Verdacht auf krebserzeugende Wirkung.

S-S?tze Betriebsanweisung:

S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S22:Staub nicht einatmen.

Chemische Eigenschaften

Off-White Crystalline Solid

Verwenden

An anti-neoplastic - inhibits ribonucleoside reductase and DNA replication. A potential therapy for sickle cell anemia which involves the nitrosylation of sickle cell hemoglobin. Horseradish peroxidase catalyzes nitric oxide formation from hydroxyurea in the presence of hydrogen peroxide.

Indications

Hydroxyurea (Hydrea) inhibits the enzyme ribonucleotide reductase and thus depletes intracellular pools of deoxyribonucleotides, resulting in a specific impairment of DNA synthesis. The drug therefore is an Sphase specific agent whose action results in an accumulation of cells in the late G1- and early S-phases of the cell cycle.

Allgemeine Beschreibung

HONH-CO-NH2. The drug is available in a 500-mg capsulefor oral use. Hydroxyurea is often considered an antimetabolitedrug, and it is used to treat myelogenousleukemia, ovarian cancer, and essential thrombocytosis. Themechanism of action of hydroxyurea involves inhibition ofDNA biosynthesis by inhibition of the enzyme ribonucleotidereductase). Resistance can occur viaincreased expression of ribonucleotide reductase. The oralbioavailability is quite high approaching 100% and the drugis distributed to all tissues. Hydroxyurea readily enters theCNS and distributes to human breast milk. A major portionof the total dose is excreted unchanged in the urine. Thedrug has been shown to increase the toxicity of 5-FU, andhydroxyurea may increase the effectiveness of some antimetaboliteHIV drugs. The toxicity profile includes myelosuppression,leucopenia, nausea, vomiting, pruritus hyperpigmentation,headache, drowsiness, and confusion.

Air & Water Reaktionen

Water soluble.

Reaktivit?t anzeigen

An amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Brandgefahr

Flash point data for Hydroxyurea are not available; however, Hydroxyurea is probably combustible.

Mechanism of action

Hydroxyurea is rapidly absorbed after oral administration, with peak plasma levels achieved approximately 1 to 2 hours after drug administration; its elimination half-life is 2 to 3 hours. The primary route of excretion is renal, with 30 to 40% of a dose excreted unchanged.

Clinical Use

Hydroxyurea is used for the rapid lowering of blood granulocyte counts in patients with chronic granulocytic leukemia. The drug also can be used as maintenance therapy for patients with the disease who have become resistant to busulfan. Only a small percentage of patients with other malignancies have had even brief remissions induced by hydroxyurea administration.

Nebenwirkungen

Hematological toxicity, with white blood cells affected more than platelets, may occur. Megaloblastosis of the bone marrow also may be observed. Recovery is rapid, generally within 10 to 14 days after discontinuation of the drug. Some skin reactions, including hyperpigmentation and hyperkeratosis, have been reported with chronic treatment.

Stoffwechsel

Hydroxyurea has excellent oral bioavailability (80–100%), and serum levels peak within 2 hours of consuming the capsules. If a positive response is noted within 6 weeks, toxicities generally are mild enough to permit long-term or indefinite therapy on either a daily or every-3-day basis. Leukopenia and, less commonly, thrombocytopenia and/or anemia are the most serious adverse effects. Excretion of the unchanged drug and the urea metabolite is via the kidneys. The carbon dioxide produced as a by-product of hydroxyurea metabolism is excreted in the expired air.

l?uterung methode

Recrystallise hydroxyurea from absolute EtOH (10g in 150mL). Note that the rate of solution in boiling EtOH is slow (15-30minutes). It should be stored in a cool dry place, but some decomposition could occur after several weeks. [Deghenghi Org Synth Coll Vol V 645 1973.] It is very soluble in H2O and can be crystallised from Et2O. [Kfod Acta Chem Scand 10 256 1956, Beilstein 3 IV 170.]

Hydroxycarbamid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Hydroxycarbamid Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 579)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Weibang Biotechnology Co., Ltd
+8615531157085
abby@weibangbio.com China 8810 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325
sales1@chuanghaibio.com China 5889 58
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
+86-18600796368 +86-18600796368
sales@sjar-tech.com China 456 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21634 55
Hubei XinRunde Chemical Co., Ltd.
+8615102730682
bruce@xrdchem.cn CHINA 566 55
Nanjing Finetech Chemical Co., Ltd.
025-85710122 17714198479
sales@fine-chemtech.com CHINA 885 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32957 60
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29880 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2930 58

127-07-1(Hydroxycarbamid)Verwandte Suche:


  • Carbamohydroximic acid
  • Hidroxicarbamida
  • Hydurea
  • N-(aminocarbonyl)hydroxylamine
  • wr 83799
  • hydrixycarbamide
  • HYDROXYUREA
  • Urea,N-hydroxy-
  • CHEBI:44423
  • Hydroxicarbamidum
  • hydroxyaminomethanamide
  • Hydroxycarbamid
  • Hydroxyharnstoff [German]
  • Hydroxyurea [USAN:BAN]
  • Idrossicarbamide [DCIT]
  • Mylocel
  • NHY
  • N-Hydroxymocovina [Czech]
  • S-phase/G-1 interface inhibitor
  • Hydroxyurea Vetec(TM) reagent grade, >=98%
  • Hydroxy urine
  • biosupressin
  • carbamohydroxamicacid
  • carbamohydroxyamicacid
  • Carbamoylhydroxylamine
  • carbamoyloxime
  • carbamylhydroxamate
  • hidrix
  • hydreia
  • hydroxycarbamine
  • hydroxyharnstoff
  • hydroxylurea
  • hydroxy-ure
  • hydroxyurea(d4)
  • hydura
  • litaler
  • litalir
  • n-(aminocarbonyl)-hydroxylamin
  • n-carbamoyl-hydroxylamin
  • n-carbamoylhydroxylamine
  • nci-c04831
  • n-hydroxymocovina
  • nsc32065
  • onco-carbide
  • oxyurea
  • sk22591
  • sq1089
  • Urea,hydroxy-
  • Hydroxyurea,98%
  • Hydroxyurea/HydroxycarbaMide
  • Hydroxyurea, 98% 25GR
  • Hydroxyurea, 98% 5GR
  • Cytodrox
  • Hydroxycarbamide (Hydroxyurea)
  • Hydroxyurea (200 mg)
  • Oxyure
  • hydroxycarbamide,HU
  • N-Hydroxyharnstoff
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