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citreoviridin

Product Name
citreoviridin
CAS No.
25425-12-1
Chemical Name
citreoviridin
Synonyms
citreoviridin;CITREOVIRIDINE;Citreoviridin A;Citreoviridine A;(-)-citreoviridin;Citreoviridin, froM PenicilliuM citreoviride biourge;Citreoviridin, 97%, from Penicillium citreoviride biourge;6-[(1E,3E,5E,7E)-8-[(2R,3R,4R,5R)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-5-methylpyran-2-one;D-Iditol, 2,5-anhydro-1,6-dideoxy-2-C-[(1E,3E,5E,7E)-8-(4-methoxy-5-methyl-2-oxo-2H-pyran-6-yl)-2-methyl-1,3,5,7-octatetraen-1-yl]-4-C-methyl-;4-Methoxy-5-methyl-6-[(1E,3E,5E,7E)-7-methyl-8-[(2S)-tetrahydro-3α,4β-dihydroxy-2,4,5β-trimethylfuran-2-yl]-1,3,5,7-octatetrenyl]-2H-pyran-2-one
CBNumber
CB01392250
Molecular Formula
C23H30O6
Formula Weight
402.48
MOL File
25425-12-1.mol
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citreoviridin Property

Melting point:
107-111℃
Boiling point:
444.62°C (rough estimate)
Density 
1.1271 (rough estimate)
refractive index 
1.4593 (estimate)
storage temp. 
2-8°C
solubility 
DMSO: 10 mg/ml; Ethanol: 10 mg/ml
form 
Yellow to orange powder.
pka
13.67±0.70(Predicted)
Stability:
Light Sensitive
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Safety

Hazard Codes 
T
Risk Statements 
63-23/24/25-36/37/38
Safety Statements 
22-26-36/37/39-45
RIDADR 
3172
RTECS 
UQ1235000
HazardClass 
6.1(a)
PackingGroup 
II
HS Code 
29322090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H300Fatal if swallowed

H311Toxic in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H331Toxic if inhaled

H335May cause respiratory irritation

H361Suspected of damaging fertility or the unborn child

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P311Call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
11319
Product name
Citreoviridin
Purity
≥95%
Packaging
1mg
Price
$61
Updated
2024/03/01
Cayman Chemical
Product number
11319
Product name
Citreoviridin
Purity
≥95%
Packaging
500μg
Price
$28
Updated
2021/12/16
Cayman Chemical
Product number
11319
Product name
Citreoviridin
Purity
≥95%
Packaging
5mg
Price
$210
Updated
2024/03/01
TRC
Product number
C520560
Product name
Citreoviridin(80%,ContainIsocitreoviridin)
Packaging
5mg
Price
$245
Updated
2021/12/16
Usbiological
Product number
C5809
Product name
Citreoviridin
Packaging
1mg
Price
$327
Updated
2021/12/16
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citreoviridin Chemical Properties,Usage,Production

Chemical Properties

Yellow powder

Uses

Citreoviridin is the dominant analogue of a family of tetraene mycotoxins with potent neurotoxic effects, produced by several species of Aspergillus and Penicillium. Citreoviridin inhibits mitochondrial ATPase and is a causative agent of cardiac beriberi.

Uses

Citreoviridin is a mycotoxin isolated from several Penicillium species that has been shown to inhibit the mitochondrial ATP synthetase system. It inhibits soluble ATPase (KD = 4.1 μM), ADP-stimulated respiration in isolated rat liver mitochondria (KD = 0.15 μM), and ATP-driven reduction of NAD+ by succinate (KD = 2 μM). Citreoviridin has been used to target ectopic ATPase activity in cancer cells in order to modulate the metabolic activity associated with tumorigenesis.[Cayman Chemical]

Definition

ChEBI: Citreoviridin is a member of 2-pyranones.

citreoviridin Preparation Products And Raw materials

Raw materials

Preparation Products

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citreoviridin Suppliers

BOC Sciences
Tel
+16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19743
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58

25425-12-1, citreoviridinRelated Search:


  • citreoviridin
  • CITREOVIRIDINE
  • 4-Methoxy-5-methyl-6-[(1E,3E,5E,7E)-7-methyl-8-[(2S)-tetrahydro-3α,4β-dihydroxy-2,4,5β-trimethylfuran-2-yl]-1,3,5,7-octatetrenyl]-2H-pyran-2-one
  • 4-Methoxy-5-methyl-6-[(1E,3E,5E,7E)-7-methyl-8-[(2S)-tetrahydro-3α,4β-dihydroxy-2,4,5β-trimethylfuran-2β-yl]-1,3,5,7-octatetrenyl]-2H-pyran-2-one
  • 4-Methoxy-5-methyl-6-[(1E,3E,5E,7E)-7-methyl-8-[(2S)-tetrahydro-3α,4β-dihydroxy-2α,4,5β-trimethylfuran-2-yl]-1,3,5,7-octatetrenyl]-2H-pyran-2-one
  • Citreoviridin A
  • 6-[(1E,3E,5E,7E)-8-[(2R,3R,4R,5R)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-5-methylpyran-2-one
  • Citreoviridin, 97%, from Penicillium citreoviride biourge
  • Citreoviridin, froM PenicilliuM citreoviride biourge
  • Citreoviridine A
  • D-Iditol, 2,5-anhydro-1,6-dideoxy-2-C-[(1E,3E,5E,7E)-8-(4-methoxy-5-methyl-2-oxo-2H-pyran-6-yl)-2-methyl-1,3,5,7-octatetraen-1-yl]-4-C-methyl-
  • (-)-citreoviridin
  • 25425-12-1
  • mycotoxin