P1639
Patulin
≥98.0% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 149-29-1
Synonym(S): Clavacin, Clavatin, Expansine, Gigantin, Leucopin, Mycoine C3, Terinin, 4-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 MG | P1639-5-MG | In Stock | ₹ 30,927.03 |
| 10 MG | P1639-10-MG | In Stock | ₹ 36,415.30 |
| 25 MG | P1639-25-MG | In Stock | ₹ 59,126.15 |
P1639 - 5 MG
In Stock
Quantity
1
Base Price: ₹ 30,927.03
GST (18%): ₹ 5,566.865
Total Price: ₹ 36,493.895
Quality Level
300
Assay
≥98.0% (HPLC)
form
powder
solubility
water: 9-11 mg/mL
antibiotic activity spectrum
fungi
Mode of action
cell membrane | interferes
storage temp.
−20°C
SMILES string
OC1OCC=C2OC(=O)C=C12
InChI
1S/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2
InChI key
ZRWPUFFVAOMMNM-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | eMolecules Medchem Express / Patulin / 1mg / 532149533 / HY-N6779 / / 149-29-1 / MFCD00005858 / 154.121 / C7H6O4 | eMolecules | ₹ 11,334.99 | |
 | Patulin solution | Supelco | ₹ 13,579.30 | |
| | Patulin solution | Supelco | ₹ 50,760.30 | |
 | 149-29-1 | 4H-FURO[3,2-C]PYRAN-2(6H)-ONE, 4-HYDROXY- | A2B Chem | ₹ 5,561.40 - ₹ 10,438.32 |
Related Products
Description
- General description: Patulin is a mycotoxin produced by a variety of molds, such as, Aspergillus and Penicillium. It is commonly found in apples. It is used as an inhibitor of potassium uptake and as an inducer of ion flux across cell membranes, potentially involving Na+-K+ dependent ATPase and to induce intra- and intermolecular protein crosslinking.
- Application: Patulin has been used:to study patulin contamination of bottled wine[1]in DNA-damaging activity of patulin in Escherichia coli[2]in molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus[3]
- Biochem/physiol Actions: Mycotoxin with anti-bacterial,[1] potassium uptake inhibitory,[2] and possibly carcinogenic[3] activities. It is used as an inhibitor of potassium uptake and as an inducer of ion flux across cell membranes, potentially involving Na+-K+ dependent ATPase and to induce intra- and intermolecular protein crosslinking.
- Other Notes: Keep container tightly closed in a dry and well-ventilated place.
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P264 - P270 - P280 - P301 + P310 - P302 + P352 - P332 + P313
Hazard Classifications
Acute Tox. 2 Oral - Skin Irrit. 2
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 300
Assay: ≥98.0% (HPLC)
form: powder
solubility: water: 9-11 mg/mL
antibiotic activity spectrum: fungi
Mode of action: cell membrane | interferes
storage temp.: −20°C
SMILES string: OC1OCC=C2OC(=O)C=C12
InChI: 1S/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2
InChI key: ZRWPUFFVAOMMNM-UHFFFAOYSA-N
Quality Level:
300
Assay:
≥98.0% (HPLC)
form:
powder
solubility:
water: 9-11 mg/mL
antibiotic activity spectrum:
fungi
Mode of action:
cell membrane | interferes
storage temp.:
−20°C
SMILES string:
OC1OCC=C2OC(=O)C=C12
InChI:
1S/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2
InChI key:
ZRWPUFFVAOMMNM-UHFFFAOYSA-N
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storage temp.: 2-8°C
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InChI: 1S/C21H20N4O3.H2O/c1-28-19-7-6-17(20(26)24-13-15-4-2-8-22-11-15)10-18(19)21(27)25-14-16-5-3-9-23-12-16;/h2-12H,13-14H2,1H3,(H,24,26)(H,25,27);1H2
InChI key: ICYQAMNVLLHURR-UHFFFAOYSA-N
Quality Level:
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form:
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solubility:
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antibiotic activity spectrum:
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storage temp.:
2-8°C
SMILES string:
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InChI:
1S/C21H20N4O3.H2O/c1-28-19-7-6-17(20(26)24-13-15-4-2-8-22-11-15)10-18(19)21(27)25-14-16-5-3-9-23-12-16;/h2-12H,13-14H2,1H3,(H,24,26)(H,25,27);1H2
InChI key:
ICYQAMNVLLHURR-UHFFFAOYSA-N