SMB01003

Cyclopenin

≥90% (LC/MS-ELSD)

Manufacturer: Sigma Aldrich

CAS Number: 20007-87-8

Synonym(S): (-)-Cyclopenin, (-)-Cyclopenine, 4-methyl-3′-phenylspiro[1H-1,4-benzodiazepine-3,2′-oxirane]-2,5-dione

Select a Size

Pack Size SKU Availability Price
1 MG SMB01003-1-MG In Stock ₹ 32,821.40

SMB01003 - 1 MG

₹ 32,821.40

In Stock

Quantity

1

Base Price: ₹ 32,821.40

GST (18%): ₹ 5,907.852

Total Price: ₹ 38,729.252

biological source

plant

Assay

≥90% (LC/MS-ELSD)

form

solid

mol wt

294.3

solubility

water: slightly soluble

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

storage temp.

−20°C

InChI

1S/C17H14N2O3/c1-19-15(20)12-9-5-6-10-13(12)18-16(21)17(19)14(22-17)11-7-3-2-4-8-11/h2-10,14H,1H3,(H,18,21)

InChI key

APLKWZASYUZSBL-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
AB09338
20007-87-8 | Spiro[3H-1,4-benzodiazepine-3,2'-oxirane]-2,5(1H,4H)-dione, 4-methyl-3'-phenyl-, (2'R,3'S)-rel-(-)-
A2B Chem ₹ 21,988.92

Description

  • General description: Cyclopenin, a benzodiazepine alkaloid, is a natural product commonly available from strains of Penicillum cyclopium, Penicillium aurantiogriseum and Penicillum corymbiferum. Existing research suggests that this Penicillium metabolite exerts various biological activities, including antibacterial, antiviral, antitumor, anti-inflammatory, and neuroprotective properties.
  • Application: It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
  • Biochem/physiol Actions: According to existing research, Cyclopenin displays selective inhibition against acetylcholinesterase (AChE). Furthermore, it demonstrates anti-inflammatory properties by inhibiting nitric oxide production, NF-κB activation, and the expression of inflammatory factors such as IL-1β, IL-6, and iNOS in brain macrophages. In an Alzheimer′s disease model, Cyclopenin exhibited the ability to rescue learning deficits induced by amyloid-β42 overexpression in flies, indicating its potential as an anti-inflammatory agent for neurodegenerative diseases[1]. Isolated from Penicillium polonicum MCCC3A00951, Cyclopenin displayed potent inhibition of influenza neuraminidase (NA) with an IC50 value of 5.02μM, suggesting its potential as a candidate for anti-influenza NA therapy[2]. Cyclopenin, identified in the fungus Penicillium auratiogriseum Sp-19, demonstrated cytotoxicity against the tsFT210 cell line at a concentration of 3 μg/mL-1, implying its potential as an antitumor agent.(3)Cyclopenin, isolated from Penicillium polonicum MCCC3A00951, exhibited strong inhibition of influenza neuraminidase (NA) with an IC50 value of 5.02μM. This suggests that Cyclopenin has the potential to be developed as an anti-influenza NA candidate.
  • Features and Benefits: High quality compound suitable for multiple research applicationsCompatible with HPLC and mass spectrometry techniques
  • Other Notes: For additional information on our range of Biochemicals, please complete this form.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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biological source:
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1S/C17H14N2O3/c1-19-15(20)12-9-5-6-10-13(12)18-16(21)17(19)14(22-17)11-7-3-2-4-8-11/h2-10,14H,1H3,(H,18,21)

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APLKWZASYUZSBL-UHFFFAOYSA-N

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1S/C36H42O19/c1-15(50-23(39)8-5-16-3-6-17(7-4-16)51-34-29(44)27(42)25(40)21(12-37)52-34)19-11-36(55-32(19)47)10-9-18-20(31(46)48-2)14-49-33(24(18)36)54-35-30(45)28(43)26(41)22(13-38)53-35/h3-11,14-15,18,21-22,24-30,33-35,37-38,40-45H,12-13H2,1-2H3/b8-5+/t15-,18+,21?,22?,24+,25?,26?,27?,28?,29?,30?,33-,34?,35?,36+/m0/s1

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AFYIWKNGSIYXCQ-PYQCQGLYSA-N

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ONDWGDNAFRAXCN-VUEDXXQZSA-N

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InChI:
__

InChI key:
__