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(-)-Pyrenophorol is a fungal metabolite derived from various species of pathogenic fungi, including Byssochlamys, Stenphyllum, Alternaria, and Drechslera. It is a simple macrocyclic dilactone with diverse biological activities, such as inhibiting human topoisomerase II α and exhibiting antibiotic, herbicidal, and anthelmintic properties. Structurally, it is closely related to the macrolide dilactone Pyrenophorol.

22248-41-5

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22248-41-5 Usage

Uses

Used in Pharmaceutical Industry:
(-)-Pyrenophorol is used as an anti-fungal antibiotic for its moderate activity against the fungus Microbotryum violaceum. It is produced by plant pathogenic fungi like Pyrenophora avenue and Stemphylium radicinum, making it a potential candidate for developing anti-fungal treatments.
Used in Agriculture:
(-)-Pyrenophorol is used as a herbicide due to its ability to inhibit seed germination and induce leaf necrosis and chlorophyll retention in wild oats when used at specific concentrations. This property makes it a potential tool for controlling weed growth in agricultural settings.
Used in Research and Development:
(-)-Pyrenophorol is used as a research compound for studying its various biological activities, such as its inhibition of human topoisomerase II α and its effects on root development and abnormal chlorophyll retention in germinated seeds. This information can be valuable for developing new drugs and understanding the compound's potential applications in medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 22248-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22248-41:
(7*2)+(6*2)+(5*2)+(4*4)+(3*8)+(2*4)+(1*1)=85
85 % 10 = 5
So 22248-41-5 is a valid CAS Registry Number.

22248-41-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-Pyrenophorol

1.2 Other means of identification

Product number -
Other names (3E,5S,8R,11E,13S,16R)-5,13-dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadeca-3,11-diene-2,10-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22248-41-5 SDS

22248-41-5Relevant academic research and scientific papers

Macrodiolide Diversification Reveals Broad Immunosuppressive Activity That Impairs the cGAS-STING Pathway

Biltoft, Mette,Jakobsen, Martin R.,Jennet, Kira M.,Kristensen, Tobias F.,Liu, Han,Ottosen, Rasmus N.,Poulsen, Thomas B.,Svenningsen, Esben B.

, p. 18734 - 18741 (2021/07/19)

The development of new immunomodulatory agents can impact various areas of medicine. In particular, compounds with the ability to modulate innate immunological pathways hold significant unexplored potential. Herein, we report a modular synthetic approach to the macrodiolide natural product (?)-vermiculine, an agent previously shown to possess diverse biological effects, including cytotoxic and immunosuppressive activity. The synthesis allows for a high degree of flexibility in modifying the macrocyclic framework, including the formation of all possible stereoisomers. In total, 18 analogues were prepared. Two analogues with minor structural modifications showed clearly enhanced cancer cell line selectivity and reduced toxicity. Moreover, these compounds possessed broad inhibitory activity against innate immunological pathways in human PBMCs, including the DNA-sensing cGAS-STING pathway. Initial mechanistic characterization suggests a surprising impairment of the STING-TBK1 interaction.

An alternative stereoselective total synthesis of (-)-pyrenophorol

Alluraiah, Gurrala,Sreenivasulu, Reddymasu,Chandrasekhar, Choragudi,Raju, Rudraraju Ramesh

, p. 2738 - 2743 (2018/09/25)

The total synthesis of 16-membered C2–Symmetric dilactone (-)-Pyrenophorol was accomplished starting from commercially available (S)-epoxide prepared by hydrolytic kinetic resolution of (±)–epoxide with key steps of Grignard reaction, Swern oxidation, Wittig reaction and cyclization was achieved by intermolecular Mitsunobu cyclization. The synthesis of (-)-Pyrenophorol accomplished from cheaply available starting material, easily work-up procedures and reduction of cost in industrial process were major advantages of this route.

Stereoselective total synthesis of (?)-pyrenophorol

Ashok, Dongamanti,Pervaram, Sridhar,Chittireddy, Venkata Ramana Reddy,Reddymasu, Sreenivasulu,Vuppula, Naresh Kumar

, p. 971 - 977 (2018/03/28)

Abstract: A simple and efficient stereoselective synthesis of macrodilactone of (?)-pyrenophorol (1) has been accomplished in 12 steps in 8.3% overall yield, from inexpensive and commercially available (S)-ethyl lactate. This convergent synthesis utilizes an oxidation–reduction protocol and cyclodimerisation under the Mitsunobu reaction conditions as key steps.

Asymmetric hydroformylation-initiated tandem sequences for syntheses of (+)-patulolide C, (-)-pyrenophorol, (+)-decarestrictine L, and (+)-prelog djerassi lactone

Risi, Roberto M.,Maza, Andrew M.,Burke, Steven D.

, p. 204 - 216 (2016/09/09)

Four different Rh-catalyzed asymmetric hydroformylation (AHF) tandem reactions have been developed in the context of the total syntheses of (+)-patulolide C, (-)-pyrenophorol, (+)-decarestrictine L, and (+)-Prelog-Djerassi lactone. A total synthesis of (+)-patulolide C has been accomplished in three steps utilizing a Rh(I)-catalyzed Z-selective anti-Markovnikov hydroacetoxylation of a known alkyne to give a Z-enol acetate with excellent selectivity. An AHF/intramolecular Wittig olefination cascade was utilized to set the C4-hydroxyl stereochemistry, E-olefin geometry, and form the macrolactone. In addition, both (-)-pyrenophorol and (+)-decarestrictine L have been synthesized from the enantiomeric (4R)- and (4S)-4-(tert-butyldimethylsiloxy)-1-pentyne in five and four steps, respectively. These syntheses feature Ru(II)-catalyzed Z-selective anti-Markovnikov hydroacetoxylation of terminal alkynes followed by AHF/Wittig olefination sequences to rapidly establish functionality and stereogenicity. A synthesis of (+)-Prelog-Djerassi lactone was accomplished in three isolations from the known 1-vinyl-4-methyl-2,6,7-trioxabicyclo[2.2.2]-octane ortho ester. An AHF/crotylation tandem sequence has been developed to set the C2-C4 stereochemistry. An asymmetric hydrogenation was employed to set the C6 stereochemistry, resulting in an especially efficient enantioselective synthesis from achiral starting material. In summary, these syntheses have greatly improved efficiency in terms of atom-economy, catalytic stereoselective transformations, inexpensive reagents, step-counts, and overall yield when compared with previous synthetic attempts.

Total synthesis of (-)-pyrenophorol

Yadav, Jhillu S.,Reddy, Ganapuram Madhusudhan,Rao, Tenneti Srinivasa,Reddy, Basi V. Subba,Al Khazim Al Ghamdi, Ahmad

, p. 783 - 787 (2012/04/10)

An efficient synthetic route has been developed for the synthesis of (-)-pyrenophorol employing Sharpless asymmetric epoxidation, olefin cross-metathesis, and intermolecular Mitsunobu cyclization. Georg Thieme Verlag Stuttgart · New York.

Stereoselective total synthesis of (-)-pyrenophorol

Yadav,Subba Reddy,Subba Reddy

scheme or table, p. 5984 - 5986 (2010/02/28)

An efficient stereoselective total synthesis of (-)-pyrenophorol 1 is described. The key steps involved in this synthesis are hydrolytic kinetic resolution (HKR), MacMillan α-hydroxylation, Horner-Wadsworth-Emmons (HWE) reaction, and Mitsunobu cyclization

A New Approach to the Synthesis of γ-Hydroxy-α,β-unsaturated Macrolides and (-)-Pyrenophorin by Intramolecular C=C Bond Formation with Oxidative Functionalization from ω-alkanal

Nokami, Junzo,Taniguchi, Takuya,Gomyo, Shintaro,Kakihara, Toshio

, p. 1103 - 1106 (2007/10/02)

The title compounds were prepared via the intramolecular condensation reaction of 12-tridecanal(or dodecanal) or via the combination of inter- and intramolecular condensation of 5-hexanal in the presence of piperidine.

Preparation of macrodiolides via a common chiral building block. Total synthesis of (-)-pyrenophorin and (-)-pyrenophorol

Machinaga, Nobuo,Kibayashi, Chihiro

, p. 841 - 844 (2007/10/02)

Macrodiolides (-)-pyrenophorin and (-)-pyrenophorol have been synthesized utilizing a C2 symmetric (R,R)-diepoxide as a common enantiopure chiral building block.

Total synthesis of the macrodiolide pyrenophorol

Dommerholt,Thijs,Zwanenburg

, p. 1499 - 1502 (2007/10/02)

By means of a total synthesis, the absolute configuration of the naturally occurring macrodiolide pyrenophorol has been established. An essential step is the photo-induced rearrangement of an α,β-epoxy diazomethyl ketone to produce a 4-hydroxy-2-alkenoate. The two lactone units have been introduced in two successive steps.

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