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Name |
Candicidin (200 MG) |
EINECS | 215-763-7 |
CAS No. | 1403-17-4 | Density | 1.3 g/cm3 |
PSA | 97.99000 | LogP | 3.43300 |
Solubility | 13.47g/L(21 oC) | Melting Point |
N/A |
Formula | C21H36O5 | Boiling Point | 1273.3 °C at 760 mmHg |
Molecular Weight | 1440.69 | Flash Point | 723.8 °C |
Transport Information | N/A | Appearance | COA |
Safety | Poison by intraperitoneal route. Moderately toxic by ingestion and subcutaneous routes. Experimental teratogenic data reported. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Candeptin;Candimon; NSC 94219; Vanobid |
Chemistry informtion about Candicidin (200 MG) (1403-17-4) is:
Synonyms: Candeptin;Candicidin;Candimon;Candizidin;Candicidin (200MG);Candicidine;Carboprst;Candicidin
MF:C63H85N21O19
EINECS: 215-763-7
Following is the molecular structure of Candicidin (200 MG) (1403-17-4) is:
Mixture of antifungal heptaene macrolides from Streptomyces griseus or Actinomyces levoris used topically in candidiasis. The antibiotic complex is composed of candicidins A, B, C, and D, of which D is the major component.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
mouse | LD50 | intraperitoneal | 14mg/kg (14mg/kg) | | Antibiotics Annual. Vol. 2, Pg. 980, 1954/1955. |
mouse | LD50 | oral | 1gm/kg (1000mg/kg) | | Antibiotiki. Vol. 14, Pg. 932, 1969. |
mouse | LD50 | subcutaneous | 160mg/kg (160mg/kg) | | Progress in Medical Chemistry. Vol. 14, Pg. 105, 1977 |
rat | LD50 | oral | 2900mg/kg (2900mg/kg) | | Antibiotiki. Vol. 14, Pg. 932, 1969. |