(Z)-Lachnophyllum lactone

(Z)-Lachnophyllum lactone
Product Name (Z)-Lachnophyllum lactone
CAS No.: 81122-95-4
Catalog No.: CFN97868
Molecular Formula: C10H10O2
Molecular Weight: 162.2 g/mol
Purity: >=98%
Type of Compound: Lipids
Physical Desc.: Oil
Targets: Antifection
Source: The herbs of Conyza stricta
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
4(Z)-Lachnophyllum lactone shows anti-fungi activity.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    (Z)-Lachnophyllum lactone

    Catalog No: CFN97868
    CAS No: 81122-95-4
    Price: Inquiry(manager@chemfaces.com)
    Journal of Agricultural and Food Chemistry, 2012, 60(23):5893-5898.
    Bioassay-Directed Isolation and Identification of Phytotoxic and Fungitoxic Acetylenes from Conyza canadensis.[Reference: WebLink]
    Conyza canadensis (L.) Cronquist syn. (horseweed) is a problematic and invasive weed with reported allelopathic properties.
    METHODS AND RESULTS:
    To identify the phytotoxic constituents of the aerial parts, a systematic bioactivity-guided fractionation of the dichloromethane extract was performed. Three active enyne derivatives, (2Z,8Z)-matricaria acid methyl ester, (4Z,8Z)-matricaria lactone, and 4(Z)-Lachnophyllum lactone, were identified. The lactones inhibited growth of the monocot Agrostis stolonifera (bentgrass) and the dicot Lactuca sativa (lettuce) at 1 mg mL(-1), while the (2Z,8Z)-matricaria acid methyl ester was less active. In a dose-response screening of the lactones for growth inhibitory activity against Lemna paucicostata ,4(Z)-Lachnophyllum lactone was the most active with an IC(50) of 104 μM, while the (4Z,8Z)-matricaria lactone was less active (IC(50) of 220 μM). In a fungal direct bioautography assay, the two lactones at 10 and 100 μg/spot inhibited growth of the plant pathogenic fungi Colletotrichum acutatum , Colletotrichum fragariae , and Colletotrichum gloeosporioides .
    CONCLUSIONS:
    In a dose-response screening of the lactones against six different plant pathogenic fungi, (4Z,8Z)-matricaria lactone was more active than the commercial fungicide azoxystrobin on Col. acutatum , Col. fragariae , and Col. gloeosporioides at 30 μM and about as active as the commercial fungicide captan against Col. gloeosporioides , while 4(Z)-Lachnophyllum lactone was less active.
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