CAS 80890-47-7|concanamycin A

Introduction:Basic information about CAS 80890-47-7|concanamycin A, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Nameconcanamycin A
CAS Number80890-47-7Molecular Weight866.09
Density1.2±0.1 g/cm3Boiling Point966.4±65.0 °C at 760 mmHg
Molecular FormulaC46H75NO14Melting Point179-180℃ (dichloromethane ethanol )
MSDSChineseUSAFlash Point538.3±34.3 °C
Symbol
GHS06
Signal WordDanger

Names

Nameconcanamycin A
SynonymMore Synonyms

concanamycin A BiologicalActivity

DescriptionConcanamycin A (Antibiotic X 4357B; Concanamycin; X 4357B) is a macrolide antibiotic and a specific vacuolar type H+-ATPase (V-ATPase) inhibitor[1].
Related CatalogResearch Areas >>CancerSignaling Pathways >>Membrane Transporter/Ion Channel >>Proton Pump
Target

Vacuolar type H+-ATPase[1]

References

[1]. Togashi K, et al. Concanamycin A, a vacuolar type H(+)-ATPase inhibitor, induces cell death in activated CD8(+) CTL. Cytotechnology. 1997 Nov;25(1-3):127-35.

[2]. Eswarappa SM, et al. Folimycin (concanamycin A) inhibits LPS-induced nitric oxide production and reduces surface localization of TLR4 in murine macrophages. Innate Immun. 2008 Feb;14(1):13-24.

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point966.4±65.0 °C at 760 mmHg
Melting Point179-180℃ (dichloromethane ethanol )
Molecular FormulaC46H75NO14
Molecular Weight866.09
Flash Point538.3±34.3 °C
Exact Mass865.518738
PSA225.92000
LogP3.88
Vapour Pressure0.0±0.6 mmHg at 25°C
Index of Refraction1.555
InChIKeyDJZCTUVALDDONK-VHHURPMASA-N
SMILESCC=CC1OC(O)(C(C)C(O)C(C)C2OC(=O)C(OC)=CC(C)=CC(C)C(O)C(CC)C(O)C(C)CC(C)=CC=CC2OC)CC(OC2CC(O)C(OC(N)=O)C(C)O2)C1C
Storage condition−20°C

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CB9732000
CHEMICAL NAME :
Antibiotic X 4357 B
CAS REGISTRY NUMBER :
80890-47-7
LAST UPDATED :
199712
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C46-H75-N-O14
MOLECULAR WEIGHT :
866.22

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
21 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
USXXAM United States Patent Document. (U.S. Patent Office, Box 9, Washington, DC 20231) Volume(issue)/page/year: #4076802
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2450 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
USXXAM United States Patent Document. (U.S. Patent Office, Box 9, Washington, DC 20231) Volume(issue)/page/year: #4076802

Safety Information

Symbol
GHS06
Signal WordDanger
Hazard StatementsH300 + H310 + H330-H319
Precautionary StatementsP260-P264-P280-P284-P301 + P310-P302 + P350
Personal Protective EquipmentEyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard CodesT+
Risk Phrases26/27/28-36
Safety Phrases26-36/37/39-45
RIDADRUN 3462 6.1/PG 2
WGK Germany3
RTECSCB9732000
Packaging GroupIII
Hazard Class6.1(b)

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Synonyms

antibioticx4357b
S-45A
MFCD00210037
Antibiotic A661I
(5R)-3-O-(4-O-Carbamoyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,4-dideoxy-1-C-{(2S,3R,4S)-4-[(2R,3S,4E,6E,9R,10S,11S,12R,13R,14E,16Z)-11-ethyl-10,12-dihydroxy-3,17-dimethoxy-7,9,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6,14,16-tetraen-2-yl]-3-hydroxypentan-2-yl}-4-methyl-5-[(1E)-prop-1-en-1-yl]-α-D-threo-pentopyranose
FOLIMYCIN,STREPTOMYCES SP
α-D-threo-Pentopyranose, 3-O-[4-O-(aminocarbonyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,4-dideoxy-1-C-[(1S,2R,3S)-3-[(2R,3S,4E,6E,9R,10S,11S,12R,13R,14E,16Z)-11-ethyl-10,12-dihydroxy-3,17-dimethoxy-7,9,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6,14,16-tetraen-2-yl]-2-hydroxy-1-methylbutyl]-4-methyl-5-C-[(1E)-1-propen-1-yl]-, (5R)-
A661-I
FOLIMYCIN
Antibiotic S-45A
x4357b
α-D-threo-Pentopyranose, 3-O-[4-O-(aminocarbonyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,4-dideoxy-1-C-[(1S,2R,3S)-3-[(2R,3S,4E,6E,9R,10S,11S,12R,13R,14E,16Z)-11-ethyl-10,12-dihydroxy-3,17-di methoxy-7,9,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6,14,16-tetraen-2-yl]-2-hydroxy-1-methylbutyl]-4-methyl-5-C-[(1E)-1-propen-1-yl]-, (5R)-
Concanamycin A,(3Z,5E,7R,8R,9S,10S,11R,13E,15E,17S,18R)-18-[(1S,2R,3S)-3-[(2R,4R,5S,6R)-4-[[4-O-(Aminocarbonyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]oxy]tetrahydro-2-hydroxy-5-methyl-6-(1E)-1-propenyl-2H-pyran-2-yl]-2-hydroxy-1-methylbutyl]-9-ethyl-8,10-
CONCANAMYCIN A
(5R)-3-O-(4-O-Carbamoyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,4-dideoxy-1-C-{(2S,3R,4S)-4-[(2R,3S,4E,6E,9R,10S,11S,12R,13R,14E,16Z)-11-ethyl-10,12-dihydroxy-3,17-dimethoxy-7,9,13,15-tetramethyl- 18-oxooxacyclooctadeca-4,6,14,16-tetraen-2-yl]-3-hydroxy-2-pentanyl}-4-methyl-5-[(1E)-1-propen-1-yl]-α-D-threo-pentopyranose
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