Avermectin A1a, 5-O-Demethyl-22,23-dihydro-
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- CAS-Nr.
- 71827-03-7
- Bezeichnung:
- Avermectin A1a, 5-O-Demethyl-22,23-dihydro-
- Englisch Name:
- Avermectin A1a, 5-O-demethyl-22,23-dihydro-
- Synonyma:
- Ivermectin B1a;IvermectinH2B1a;Ivermectin B1a (>85%);Ivermectin Impurity 3;Dihydroavermectin B1a;22,23-dihydroavermectin B1a in Methanol;5-O-Demethyl-22,23-dihydroavermectin A1a;22,23-Dihydro-5-O-demethylavermectin A1a;Avermectin A1a, 5-O-demethyl-22,23-dihydro-;Ivermectin 2-epimer (Dihydro Avermectin B1a)
- CBNumber:
- CB9928288
- Summenformel:
- C48H74O14
- Molgewicht:
- 875.09
- MOL-Datei:
- 71827-03-7.mol
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Avermectin A1a, 5-O-Demethyl-22,23-dihydro- Eigenschaften
- Schmelzpunkt:
- 155-157°
- Siedepunkt:
- 717.97°C (rough estimate)
- Dichte
- 1.0683 (rough estimate)
- Brechungsindex
- 1.6130 (estimate)
- storage temp.
- Store at -20°C
- L?slichkeit
- Soluble in DMSO
- Aggregatzustand
- solid
- pka
- 12.42±0.70(Predicted)
- Farbe
- white
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
Bildanzeige (GHS) |
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Alarmwort |
Achtung |
Gefahrenhinweise |
Code |
Gefahrenhinweise |
Gefahrenklasse |
Abteilung |
Alarmwort |
Symbol |
P-Code |
H301 |
Giftig bei Verschlucken. |
Akute Toxizit?t oral |
Kategorie 3 |
Achtung |
src="/GHS06.jpg" width="20" height="20" /> |
P264, P270, P301+P310, P321, P330,P405, P501 |
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Sicherheit |
P264 |
Nach Gebrauch gründlich waschen. |
P264 |
Nach Gebrauch gründlich waschen. |
P270 |
Bei Gebrauch nicht essen, trinken oder rauchen. |
P301+P310 |
BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen. |
P321 |
Besondere Behandlung |
P330 |
Mund ausspülen. |
P405 |
Unter Verschluss aufbewahren. |
P501 |
Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen. |
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Avermectin A1a, 5-O-Demethyl-22,23-dihydro- Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
Ivermectin B
1a is the main component (>80%) of the anthelmintic ivermectin, which also contains ivermectin B
1b (<20%; ). It produces antiparasitic activity by binding to glutamate-gated chloride channels expressed on nematode neurons and pharyngeal muscle cells, inducing irreversible channel opening and very long-lasting hyperpolarization/depolarization of the neuron/muscle cell, thereby blocking further function (EC
50 = 104 nM). Formulations containing ivermectin inhibit replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in Vero/hSLAM cells.
Definition
ChEBI: A macrocyclic lactone that is avermectin B1a in which the double bond present in the spirocyclic ring system has been reduced to a single bond. It is the major component of ivermectin.
Avermectin A1a, 5-O-Demethyl-22,23-dihydro- Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Avermectin A1a, 5-O-Demethyl-22,23-dihydro- Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 60)Lieferanten
71827-03-7(Avermectin A1a, 5-O-Demethyl-22,23-dihydro-)Verwandte Suche:
- 22,23-Dihydro-5-O-demethylavermectin A1a
- 5-O-Demethyl-22,23-dihydroavermectin A1a
- Dihydroavermectin B1a
- Ivermectin B1a
- IvermectinH2B1a
- (2Ae,4E,5'S,6S,6'R,7S,8E,11R,13R,15S,17ar,20R,20ar,20bs)-20,20B-dihydroxy-5',6,8,19-tetramethyl-6'-[(1S)-1-methylpropyl]-17-oxo-3',4',5',6,6',10,11,14,15,17,17A,20,20A,20B-tetradecahydro-2H,7H-spiro[11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-7-yl 2,6-dideoxy-4-o-(2,6-dideoxy-3-o-methyl-alpha-L-arabino-hexopyranosyl)-3-o-methyl-alpha-L-arabino-hexopyranoside
- Avermectin A1a, 5-O-demethyl-22,23-dihydro-
- Ivermectin Impurity 3
- Ivermectin B1a (>85%)
- Ivermectin B1a-D2Q: What is
Ivermectin B1a-D2 Q: What is the CAS Number of
Ivermectin B1a-D2
- Avermectin,Ivermectin,B1a,COVID-19,Parasite,Inhibitor,SARS coronavirus,Ivermectin B1a,anti-parasite,inhibit,SARS-CoV
- Ivermectin 2-epimer (Dihydro Avermectin B1a)
- 22,23-dihydroavermectin B1a in Methanol
- 71827-03-7
- Organics