Quinolactacin A
Product Code: AG-CN2-0164
Product Group: Natural Products and Extracts
Supplier: AdipoGen Life Sciences
| Code | Size | Price |
|---|
| AG-CN2-0164-M001 | 1 mg | £210.00 |
Quantity:
| AG-CN2-0164-M005 | 5 mg | £810.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
-20°C
Documents
Further Information
Appearance:
Yellowish powder.
CAS:
Quinolactacin A1: 386211-68-3Quinolactacin A2: 386211-69-4
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.
Hazards:
H302, H312, H319
InChi:
InChI=1S/C16H18N2O2/c1-4-9(2)13-14-12(16(20)17-13)15(19)10-7-5-6-8-11(10)18(14)3/h5-9,13H,4H2,1-3H3,(H,17,20)/t9-,13?/m0/s1
InChiKey:
FLHQAMWKNPOTDV-LLTODGECSA-N
Long Description:
Chemical. CAS: Quinolactacin A1: 386211-68-3/Quinolactacin A2: 386211-69-4. Formula: C16H18N2O2. MW: 270.3. Isolated from Penicillium citrinum. Antibiotic. Acetylcholinesterase (AChE) inhibitor. Anti-inflammatory compound. Tumor necrosis factor (TNF) inhibitor.
MDL:
MFCD28899083
Molecular Formula:
C16H18N2O2
Molecular Weight:
270.3
Other data:
Tautomerized format (mixture of Quinolactacin A1 & A2)
Package Type:
Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Antibiotic [1-3]. Acetylcholinesterase (AChE) inhibitor [3]. Anti-inflammatory compound [1, 4]. Tumor necrosis factor (TNF) inhibitor [1, 4].
Purity:
>95% (HPLC)
Signal word:
Warning
SMILES:
[H][C@](C)(CC)C1([H])NC(=O)C2=C1N(C)C1=CC=CC=C1C2=O
Solubility Chemicals:
Soluble in DMSO, ethanol or methanol.
Source / Host:
Isolated from Penicillium citrinum.
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
Quinolactacins A, B and C: Novel Quinolone Compounds from Penicillium sp. EPF-6 I. Taxonomy, Production, Isolation and Biological Properties: N. Kakinuma, et al.; J. Antibiot. 53, 1247 (2000) | Quinolactacins A, B and C: Novel Quinolone Compounds from Penicillium sp. EPF-6 II. Physico-chemical Properties and Structure Elucidation: S. Takahashi, et al.; J. Antibiot. 53, 1252 (2000) | Quinolactacins Al and A2, new acetylcholinesterase inhibitors from Penicillium citrinum: W.G. Kim, et al.; J. Antibiot. 54, 831 (2001) | Biosynthesis of quinolactacin A, a TNF production inhibitor: T. Sasaki, et al.; J. Antibiot. 59, 418 (2006)
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