ChemicalBook--->CAS DataBase List--->101043-37-2

101043-37-2

101043-37-2 Structure

101043-37-2 Structure
IdentificationBack Directory
[Name]

MICROCYSTIN-LR
[CAS]

101043-37-2
[Synonyms]

MC-LR
C05371
MCYST-LR
akerstox
toxin-lr
microcystin-a
MICROCYSTIN-LR
CYANOGINOSIN-LR
Microcystin LR 95%
TOXIN,BLUE-GREENALGA
CYANOGINOSIN-LR;MC-LR
microcystin-lr solution
5-L-Arginine-cyanoginosin
5-l-arginine-cyanoginosinl
5-l-argininecyanoginosinla
microcystisaeruginosatoxin
5-L-ARGININE-MICROCYSTIN LA
toxini(microcystisaeruginosa)
toxint17(microcystisaeruginosa)
Cyanoginosin, Fast-death factor
MICROCYSTIN-LR, MICROCYSTIS AERUGINOSA
toxin,bluegreenalga,microcystisaeruginosa
microcystin lr from microcystis aeruginosa
Microcystin LR Solution in Methanol,10μg/mL
Microcystin-LR solution 10 UG/ML IN METHANOL
Microcystin-LR solution,Cyanoginosin, Fast-death factor
Cyclo[D-Ala-L-Leu-[(3S)-3-methyl-D-βAsp-]-L-Arg-[(2S,3S)-2-methyl-3-[(1E,3E,5S,6S)-3,5-dimethyl-6-methoxy-7-phenyl-1,3-heptadiene-1-yl]-βAla-]-D-γGlu-N-methyl-Dha-]
cyclo[2,3-didehydro-N-methylalanyl-D-alanyl-L-leucyl-(3S)-3-methyl-D-β-aspartyl-L-arginyl-(2S,3S,4E,6E,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-4,6-decadienoyl-D-γ-glutamyl
cyclo[2,3-didehydro-N-methylalanyl-D-alanyl-L-leucyl-(3S)-3-methyl-D-β-aspartyl-L-arginyl-(2S,3S,4E,6E,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-4,6-decadienoyl-D-γ-glutamyl]
(5R,8S,11R,12S,15S,18S,19S,22R)-15-(3-guanidinopropyl)-8-isobutyl-18-((1E,3E,5S,6S)-6-methoxy-3,5-dimethyl-7-phenylhepta-1,3-dien-1-yl)-1,5,12,19-tetramethyl-2-methylene-3,6,9,13,16,20,25-heptaoxo-1,4,7,10,14,17,21-heptaazacyclopentacosane-11,22-dicarboxy
(5R,8S,11R,12S,15S,18S,19S,22R)-15-(3-guanidinopropyl)-8-isobutyl-18-((1E,3E,5S,6S)-6-methoxy-3,5-dimethyl-7-phenylhepta-1,3-dien-1-yl)-1,5,12,19-tetramethyl-2-methylene-3,6,9,13,16,20,25-heptaoxo-1,4,7,10,14,17,21-heptaazacyclopentacosane-11,22-dicarboxylic acid
[EINECS(EC#)]

621-323-9
[Molecular Formula]

C49H74N10O12
[MDL Number]

MFCD00131607
[MOL File]

101043-37-2.mol
[Molecular Weight]

995.17
Chemical PropertiesBack Directory
[density ]

1.29±0.1 g/cm3(Predicted)
[Fp ]

11 °C
[storage temp. ]

−20°C
[solubility ]

ethanol: 1 mg/mL
[form ]

solid film
[pka]

3.03±0.70(Predicted)
[color ]

Off-white
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO, methanol or ethanol may be stored at -20°C for up to 2 months.
[IARC]

2B (Vol. 94) 2010
[EPA Substance Registry System]

Microcystin LR (101043-37-2)
Safety DataBack Directory
[Hazard Codes ]

T+,T,F
[Risk Statements ]

26/27/28-36/37/38-43-39/23/24/25-23/24/25-11
[Safety Statements ]

26-36/37/39-45-36/37-16-7
[RIDADR ]

UN 2811 6.1/PG 1
[WGK Germany ]

3
[RTECS ]

GT2810000
[HS Code ]

30029090
[Hazardous Substances Data]

101043-37-2(Hazardous Substances Data)
[Toxicity]

LD50 orl-rat: >5 mg/kg HETOEA 18,162,1999
Hazard InformationBack Directory
[Hazard]

A poison by ingestion and inhalation.
[Description]

Microcystins are hepatotoxic cyclic heptapeptide toxins produced by cyanobacteria. They are responsible for periodic poisonings of humans and livestock drinking fresh water where the blue-green algae are endemic. Microcystin-LR is a selective inhibitor of protein phosphatase 2A (PP2A) (IC50= 0.04 nM) and will completely inhibit this enzyme without affecting PP1 when used at a concentration of 0.5 nM. The PP1 IC50 is about 1.7 nM. Microcystins are at least 10 times more potent as serine/threonine PP inhibitors than okadaic acid, another microalgal toxin also used for this purpose.
[Definition]

ChEBI: Microcystin-LR is a microcystin consisting of D-alanyl, L-leucyl, (3S)-3-methyl-D-beta-aspartyl,L-arginyl, 2S,3S,4E,6E,8S,9S)-3-amino-4,5,6,7-tetradehydro-9-methoxy-2,6,8-trimethyl-10-phenyldecanoyl, D-gamma-glutamyl, and 2,3-didehydro-N-methylalanyl residues joined into a 25-membered macrocycle. Produced by the cyanobacterium Microcystis aeruginosa, it is the most studied of the microcystins. It has a role as a bacterial metabolite, an EC 3.1.3.16 (phosphoprotein phosphatase) inhibitor, a xenobiotic and an environmental contaminant.
[Safety Profile]

A poison by ingestion, inhalation,intraperitoneal, and intravenous route. Experimentalreproductive effects. When heated to decomposition itemits toxic vapors of NOx.
[References]

1) Rinehart?et al.?(1988),?Nodularin, microcystin, and the configuration of Adda; J. Am. Chem. Soc.,?110?8557 2) Honkanen?et al. (1990),?Characterization of microcystin-LR, a potent inhibitor of type 1 and type 2A protein phosphatases;?J. Biol. Chem,?265?19401 3) Runnegar?et al.?(1995),?Microcystin uptake and inhibition of protein phosphatases: effects of chemoprotectants and self-inhibition in relation to known hepatic transporters; Toxicol. Appl. Pharmacol.,?134?264
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