PEER-REVIEW ARTICLE PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5870 Mitigation of Methanogenesis in Ruminants Using Wheatgrass Compounds as Methyl Coenzyme M Reductase Inhibitors: An In Silico Study Ananya Saluguti,a Ameer Khusro,b,* Prabhalakshmi Balasubramaniyan,a Dhanraj Ganapathy,a Maximilian Lackner,c,* and Moises Cipriano-Salazar d Ruminants are significant contributors to methane (CH4) emissions due to methanogenesis by their gut microbiomes. The enzyme methyl coenzyme M reductase (MCR) is crucial for this process in rumen archaea. Targeting MCR via computational tools has emerged as a novel approach to reduce CH4 emissions in ruminants by inhibiting methanogenesis. This study focused on evaluating wheatgrass (Thinopyrum intermedium) compounds as potential MCR inhibitors using in silico methods. Initially, 21 wheatgrass compounds were selected, and their drug-likeness traits were assessed using Lipinski’s rule of five. Five compounds, namely 2,4,6-trimethyl-1,3- phenylenediamine, Caryophyllene oxide, Caryophyllene, N,N- tetramethylene-.alpha.-(aminomethylene) glutaconic anhydride, and n- hexadecanoic acid met all criteria. These compounds were further analysed for absorption, distribution, metabolism, and excretion (ADME) properties using the Swiss ADME tool, confirming their drug-likeness traits with no Lipinski’s violation. Molecular docking analysis was performed using the CB-Dock2 tool to assess binding interactions with MCR. The compounds showed binding affinities in the following order: N,N- tetramethylene-.alpha.-(aminomethylene) glutaconic anhydride (-7.3 kcal/mol) > Caryophyllene (-6.8 kcal/mol) > Caryophyllene oxide (-6.7 kcal/mol) > n-hexadecanoic acid (-6.3 kcal/mol) > 2,4,6-trimethyl-1,3- phenylenediamine (-6.0 kcal/mol). These findings suggest that the selected wheatgrass compounds have potential as anti-methanogenic agents, positioning them as promising MCR inhibitors for mitigating CH4 emissions in ruminants. DOI: 10.15376/biores.20.3.5870-5883 Keywords: Anti-methanogenic agent; CB-Dock2 tool; Methyl coenzyme M reductase; Ruminants; Swiss ADME tool; Wheatgrass Contact information: a: Dept. of Prosthodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai – 600077, India; b: Dept. of Research Analytics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai – 600077, India; c: Dept. of Industrial Engineering, University of Applied Sciences Technikum Wien, Hoechstaedtplatz 6, 1200 Vienna, Austria; d: Facultad de Medicina Veterinaria y Zootecnia No. 1, Universidad Autónoma de Guerrero, Guerrero, México; *Corresponding author: armankhan0301@gmail.com / maximilian.lackner@technikum-wien.at INTRODUCTION There is no doubt that ruminants are crucial for human life as they convert indigestible plant biomass into digestible products like milk and meat (Kamra et al. 2012). With rising global demand for these products due to population growth and improved lifestyles (Lan and Yang 2019), the number of domesticated ruminants has significantly PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5871 increased. However, this surge raises concerns among ecologists and veterinarians about the associated greenhouse gas emissions, especially methane (CH4) production. As a matter of fact, the emission of CH4 from ruminants is directly proportional to the ruminants’ population (Islam and Lee 2019). Methane is a potent greenhouse gas, revealing a 25 times higher global warming effect than that of carbon dioxide (CO2), and ruminants contribute to 16% of global greenhouse gas emissions, accounting for 33% of anthropogenic CH4 emission (Lan and Yang 2019). The rumen, an anaerobic fermenter, hosts a diverse microbial community, including bacteria, protozoa, fungi, and archaea (Islam and Lee 2019). Protozoa can constitute up to 50% of the rumen’s microbial biomass (Newbold et al. 2015), while fungi typically make up around 8%, potentially reaching 20% in sheep (Orpin 1981; Rezaeian et al. 2004). Archaea account for a smaller fraction, about 0.3 to 4% (Janssen and Kirs 2008), with bacteria comprising the majority of the microbial biomass (Tapio et al. 2017). This microbiome is crucial for fermenting carbohydrates-based feed, producing volatile fatty acids (acetic acid, propionic acid, butyric acids, etc.), CO2, and hydrogen (H2), which are essential for the ruminant’s energy metabolism (Lan and Yang 2019). Methanogenesis is the process by which CH4 is produced in the rumen, primarily through the reduction of CO2 by H2, facilitated by methanogenic archaea. This process is crucial for clearing H2 from fermentation (Islam and Lee 2019). Methanogenesis occurs via two main pathways: the hydrogenotrophic and methylotrophic pathways (Fig. 1). In the hydrogenotrophic pathway, H2 and CO2 are converted into CH4 by rumen microorganisms, such as bacteria, protozoa, and fungi (Martin et al. 2010). Formate, which can be utilized by most ruminal archaea similarly to H2 and CO2, is also included in this category (Janssen 2010). The methylotrophic pathway, on the other hand, involves the conversion of methyl groups from substrates like methylamines and methanol into CH4 (Poulsen et al. 2013). Fig. 1. Methane production from ruminants through (A) hydrogenotrophic pathway and (B) methylotrophic pathway A variety of methanogens, including species, such as Methanobacterium spp., Methanobrevibacter spp., and Methanosarcina spp., are involved in the final stage of carbohydrate degradation in the rumen, where they convert H2 and other compounds like formate, CO2, or methyl donors into CH4 (Poulsen et al. 2013). The final step in biological CH4 synthesis is catalyzed by the enzyme methyl-coenzyme M reductase (MCR; PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5872 EC 2.8.4.1), a membrane-associated enzyme that is unique to methanogens and play a central role in CH4 biogeochemistry (Khusro et al. 2022a). The enzyme is composed of three subunits: α (mcrA), β (mcrB), and γ (mcrG). The α-subunit, encoded by the mcrA gene, is highly conserved across all methanogens. This enzyme catalyzes the reduction of methyl coenzyme M (methyl-S-CoM) to CH4, with coenzyme B serving as the electron donor and coenzyme F430 (a nickel-containing tetrahydrocorphin) acting as the prosthetic group (Casañas et al. 2015). In recent years, plethora of in vitro studies has been carried out to suppress CH4 production from ruminants by adding disparate dietary supplements in the feed (Khusro et al. 2022b; Elghandour et al. 2023, 2024; Santillán et al. 2023). However, mitigating CH4 emission by manipulating the biochemical pathway of methanogenesis process spotlights a new dimension in addressing anti-methanogenic trait in ruminants. Surprisingly, the mitigation of CH4 emission from ruminants by targeting MCR receptor via computational tool is limited. In view of this, the present context was assessed to predict the anti- methanogenic attribute of wheatgrass (Thinopyrum intermedium)-associated compounds against MCR receptor in ruminants via in silico tools. EXPERIMENTAL Compounds of interest A total of 21 compounds were identified from wheatgrass leaf extract based on previous studies (Durairaj et al. 2014; Shakya et al. 2014). The chemical structures of these compounds were obtained from PubChem (https://pubchem.ncbi.nlm.nih.gov/) in SDF format and were used for the subsequent analyses (Fig. 2). Fig. 2. List of selected wheatgrass compounds PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5873 Ligands Selection Lipinski’s rule of five Lipinski’s rule of five was applied to assess the drug-likeness of all the ligands (http://www.scfbio-iitd.res.in/software/drugdesign/lipinski.jsp). This rule evaluates the drug’s viability by considering factors, such as molecular weight, logP, number of hydrogen bond acceptors, hydrogen bond donors, and molar refractivity (Lipinski 2004). ADME properties analysis Ligands that satisfied Lipinski’s rule of five were further analysed for ADME (absorption, distribution, metabolism, and excretion) properties analysis using the Swiss ADME tool from the Swiss Institute of Bioinformatics (http://www.swissadme.ch/). Canonical SMILES for the ligands were retrieved from PubChem and evaluated for properties such as water solubility (Log mol/L), lipophilicity (Log Po/w), gastrointestinal (GI) absorption, blood brain barrier (BBB) permeant, and P-gp substrate status. The Swiss ADME tool, based on a support vector machine algorithm, efficiently analyses datasets of known inhibitor/non-inhibitor and substrate/non-substrate (da Silva et al. 2006). These selected compounds were then advanced to molecular docking analysis. In silico Molecular Docking Target receptor The structure of the MCR receptor was obtained from the RCSB PDB (Research Collaboratory for Structural Bioinformatics Protein Data Bank - IMRO) (http://www.rscb.org/pdb) and saved in PDB format. Prior to docking, non-essential components, such as water molecules and bound inhibitors, were removed from the receptor structure to ensure accurate docking results (Fig. 3). Fig. 3. 3D structure of MCR receptor Molecular docking and visualization The interaction between the selected protein and ligands was analyzed using the Cavity detection-guided Blind Docking2 (CB-Dock2) tool (Liu et al. 2020). This web- based tool automatically identifies protein cavities, calculates their centers and sizes, and focuses on the top five cavities by default. Blind docking was used to explore potential binding sites and ligand-binding modes by scanning the entire protein surface (Bultum et PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5874 al. 2022). CB-Dock2 customizes the docking box based on the query ligand and performs molecular docking using AutoDock Vina (Liu et al. 2020). The lowest vina score (kcal/mol), typically associated with the largest cavity, was selected as the optimal result for each ligand. RESULTS AND DISCUSSION Lipinski’s Rule of Five for Compounds The use of diversified additives in expensive feed formulations, along with the need to assess their CH4 mitigation potential through in vitro or in vivo experiments, can be both time-consuming and costly. To address this, researchers are exploring alternative strategies for rapid screening of anti-methanogenic agents. Computational tools have emerged as an effective alternative for veterinarians, helping save time and resources. These short-term in silico approaches aim to identify suitable additives without the high cost or duration of traditional testing methods. Through developing cost-effective and efficient screening techniques, it becomes possible to find viable solutions for reducing CH4 emissions in ruminants while maintaining productivity. In this investigation, all selected wheatgrass compounds were initially evaluated for drug-likeness properties using Lipinski’s rule of five. According to drug-likeness criteria, an ideal ligand should have a molecular mass under 500 Da, fewer than 5 hydrogen bond donors, fewer than 10 hydrogen bond acceptors, lipophilicity (log p) below 5, and molar refractivity between 40 and 130 (Abhishek Biswal et al. 2019). Table 1 presents key parameters, such as molecular weight, logP, hydrogen bond acceptors, hydrogen bond donors, and molar refractivity of each compound. Among the tested compounds, 2,4,6- trimethyl-1,3-phenylenediamine, Caryophyllene oxide, Caryophyllene, N,N- tetramethylene-.alpha.-(aminomethylene)glutaconic anhydride, and n-hexadecanoic acid met the essential criteria of Lipinski’s rule of five, indicating potential for further analyses. Table 1. Wheatgrass Compounds Analysed by Lipinski’s Rule of Five Phytocomponents Molecular Formula / Mass (g/mol) logP Number of Hydrogen Bond Acceptors Number of Hydrogen Bond Donors Molar Refractivity 1,4-benzenediol, 2-methyl- C7H8O2 / 124.14 0.754 2 2 32.35 1-nonadecene C19H38 / 266.5 5.962 0 0 102.25 2,4,6-trimethyl-1,3- phenylenediamine C9H14N2 / 150.22 1.794 0 4 48.2 2-methyloctacosane C29H60 / 408.8 9.138 0 0 160.6 Alpha-Amyrin C30H50O / 426.7 7.826 1 1 153.43 Beta-Amyrin C30H50O / 426.7 7.837 1 1 153.38 Caryophyllene oxide C15H24O / 220.35 3.486 1 0 74.46 Caryophyllene C15H24 / 204.35 3.961 0 0 75.11 PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5875 Clionasterol C29H50O / 414.7 7.745 1 1 150.19 D-alpha-tocopherol C29H50O2 / 430.7 7.658 2 1 150.71 Didodecyl phthalate C32H54O4 / 502.8 8.34 4 0 164.91 Eicosane, 10-heptyl-10- octyl- C35H72 / 492.9 - 0.053 6 5 77.14 Ethyl linolenate C20H34O2 / 306.5 5.297 2 0 103.6 Linolenic acid C18H30O2 / 278.4 4.325 2 1 92.19 N,N-tetramethylene-.alpha.- (aminomethylene)glutaconic anhydride C10H11NO3 / 193.2 1.056 3 0 48.07 n-hexadecanoic acid C16H32O2 / 256.4 4.325 2 1 88.26 Nonacosane C29H60 / 408.8 9.128 0 0 160.65 Octadecane, 9-ethyl-9- heptyl- C27H56 / 380.7 8.536 0 0 149.61 Triacontane C30H62 / 422.8 9.434 0 0 166.12 Phytol C20H40O / 296.5 5.721 1 1 109.16 Squalene C30H50 / 410.7 8.21 0 0 152.12 ADME Properties Analysis Table 2 presents the ADME properties of five selected wheatgrass compounds, highlighting their drug-likeness traits. All compounds demonstrated favourable traits, including water solubility, high GI absorption, lipophilicity, BBB permeability, P-gp substrate status, and no Lipinski’s rule violations. All the phytocomponents were reported as water-soluble in nature. The lipophilicity values (log Po/w) of 2,4,6-trimethyl-1,3- phenylenediamine, Caryophyllene oxide, Caryophyllene, N,N-tetramethylene-.alpha.- (aminomethylene)glutaconic anhydride, and n-hexadecanoic acid were 1.64, 3.15, 3.25, 1.65, and 3.85, respectively. All compounds displayed high GI absorption, while 2,4,6- trimethyl-1,3-phenylenediamine, Caryophyllene oxide, Caryophyllene, and n- hexadecanoic acid showed BBB permeability. Caryophyllene and N,N-tetramethylene- .alpha.-(aminomethylene)glutaconic anhydride did not permeate the BBB. None of the compounds were P-gp substrates, and there were no violations of Lipinski’s rule of five. https://pubchem.ncbi.nlm.nih.gov/#query=C18H30O2 PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5876 Table 2. ADME Properties of Five Selected Compounds Phytocomponents Water Solubility (Log mol/L) Lipophilicity (Log Po/w) GI Absorption BBB Permeant P-gp Substrate Lipinski’s Violation Drug Likeness 2,4,6-trimethyl-1,3- phenylenediamine -2.21 (Soluble) 1.64 High Yes No 0 Yes Caryophyllene oxide -3.45 (Soluble) 3.15 High Yes No 0 Yes Caryophyllene -3.87 (Soluble) 3.25 Low No No 0 Yes N,N- tetramethylene- .alpha.- (aminomethylene)gl utaconic anhydride -1.6 (Very Soluble) 1.65 High No No 0 Yes n-hexadecanoic acid -5.02 (Moderate soluble) 3.85 High Yes No 0 Yes Molecular Docking and Visualization Molecular docking of specific ligands with target receptors has proved to be an ideal, cost-efficient screening technique in diverse areas (Khusro et al. 2020a; Lavanya et al. 2023; Ramasubburayan et al. 2023; Mukundh et al. 2024). Methanogens rely on MCR for the methanogenesis process, making MCR a prime target for computational approaches aimed at reducing CH4 emissions in animals. In the present study, the binding affinity energies or docking score, cavity volume, interacting amino acid residues, docking centre, and docking size between selected wheatgrass compounds and receptor are shown in Table 3. Table 3. Docking Score, Cavity Volume, Interacting Amino Acid Residues, Docking Centre, and Docking Size Between Five Selected Compounds and MCR Receptor S. No. Compounds Docking Score (kcal/mol) Cavity Volume (Å3) Interacting Amino Acid Residues Docking Centre (x, y, z) Docking Size (x, y, z) 1. 2,4,6-trimethyl- 1,3- phenylenediami ne -6.0 6348 Chain A: GLN147 MET150 MET233 ILE236 ALA243 GLY244 THR248 Chain D: VAL328 GLY329 PHE330 THR331 GLN332 TYR333 ALA334 PHE396 GLY397 GLY398 SER399 PHE443 TYR444 Chain E: PHE361 HIS364 SER365 ILE366 TYR367 Chain F: LEU117 ARG120 23, 37, - 52 35, 25, 35 2. Caryophyllene oxide -6.7 6348 Chain A: VAL146 GLN147 ARG225 MET233 ILE236 ALA243 GLY244 THR248 ALA252 TYR253 LYS256 ALA258 VAL260 Chain D: ARG270 TYR333 PHE443 TYR444 23, 37, - 52 35, 25, 35 PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5877 Chain E: PHE361 HIS364 SER365 ILE366 TYR367 GLY368 GLY369 HIS379 Chain F: LEU117 ARG120 SER154 VAL155 3. Caryophyllene -6.8 6348 Chain A: GLN147 MET150 ARG225 ALA243 ALA252 TYR253 Chain D: MET324 TYR333 PHE396 GLY397 GLY398 SER399 GLY442 PHE443 TYR444 Chain E: PHE362 GLY368 GLY369 VAL381 Chain F: LEU117 SER118 GLY119 ARG120 VAL155 HIS156 GLY157 HIS158 SER159 23, 37, - 52 35, 25, 35 4. N,N- tetramethylene- .alpha.- (aminomethyle ne)glutaconic anhydride -7.3 6348 Chain A: GLN147 MET150 ARG225 TYR253 LYS256 Chain D: LEU320 MET324 SER325 GLY329 PHE330 THR331 GLN332 TYR333 PHE396 GLY397 GLY398 SER399 GLY442 PHE443 ASN474 ALA479 MET480 ASN481 VAL482 Chain E: PHE361 PHE362 TYR367 GLY368 GLY369 ILE380 VAL381 Chain F: LEU117 SER118 GLY119 ARG120 VAL155 HIS156 HIS158 23, 37, - 52 35, 25, 35 5. n- hexadecanoic acid -6.3 6348 Chain A: PRO268 ARG270 TRP319 LEU320 MET324 SER325 PHE330 TYR333 GLY397 GLY398 SER399 LEU441 GLY442 PHE443 TYR444 PRO473 ASN474 ALA479 MET480 ASN481 VAL482 Chain B: GLU186 PHE361 PHE362 HIS364 SER365 ILE366 TYR367 GLY368 GLY369 GLY370 ILE374 HIS379 ILE380 VAL381 Chain C: LEU117 SER118 GLY119 ARG120 VAL155 Chain D: GLN147 ARG225 MET229 MET233 ILE236 ALA243 GLY244 TYR253 LYS256 24, 38, - 14 34, 35, 35 The compound 2,4,6-trimethyl-1,3-phenylenediamine, Caryophyllene oxide, Caryophyllene, N,N-tetramethylene-.alpha.-(aminomethylene)glutaconic anhydride, and n-hexadecanoic acid predicted binding energy score of -6.0, -6.7, -6.8, -7.3, and -6.3 PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5878 kcal/mol, respectively. Figure 4 shows the 3D interaction views between compounds and MCR receptor. This is the first in silico investigation to predict the CH4-mitigating potential of wheatgrass-derived bioactive compounds by targeting MCR as the receptor. Fig. 4. Molecular docking visualization of: (a) 2,4,6-trimethyl-1,3-phenylenediamine, (b) Caryophyllene oxide, (c) Caryophyllene, (d) N,N-tetramethylene-.alpha.-(aminomethylene) PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5879 glutaconic anhydride, and (e) n-hexadecanoic acid with MCR receptor Previous in silico studies highlighted the anti-methanogenic potential of varied plant metabolites by targeting MCR. For instance, Arokiyaraj et al. (2019) identified 9,10- anthracenedione, 1,8-dihydroxy-3-methyl, phthalic acid isobutyl octadecyl ester, and diisooctyl phthalate from Rheum sp. as promising anti-methanogenic agents in ruminants through molecular modeling. Similarly, Dinakarkumar et al. (2021) analyzed 168 compounds from 11 plants, targeting MCR to mitigate CH4 emissions in ruminants. The study identified rosmarinic acid, biotin, α-cadinol, and 2,4,7,9-tetramethyl-5decyn4,7diol as the most effective MCR inhibitors. Khusro et al. (2020b) further demonstrated the pivotal role of compounds like 3,5-bis(1,1-dimethylethyl)-phenol, kaempferol, moringyne, niazimisin, and tetradecanoic acid from Moringa oleifera in reducing CH4 emissions in horses by showing strong binding interactions with MCR using Hex 8.0.0 software. Moreover, bioactive compounds, such as acacetin, matairesinol, methyl tetradecanoate, cis-6-nonenal, syringic acids, limonene, trans-2,4-decadienal, 3-isopropyl-6- methylenecyclohex-1-ene, and 2,5-octanedione, from safflower oil also exhibited strong interaction with MCR, indicating their potential as anti-methanogenic agents in the equine industry (Khusro et al. 2022a). Methanogenesis occurs in natural anaerobic environment and within the digestive tracts of animals, particularly ruminants (Alvarado et al. 2014). During this process, methanogens convert varied substrates into CH4 to obtain energy for their growth and metabolism. Annually, approximately 600 million metric tons of CH4 are released into the ecosystem through methanogenesis (Khusro et al. 2022a). The global warming potential of CH4 is about 25 times greater than that of CO2, making CH4 production a significant environmental threat (Lan and Yang 2019). In agriculture, CH4 emission from enteric fermentation in ruminants are the largest single source of greenhouse gases and one of the most significant anthropogenic contributors (Palangi and Lackner 2022). Given its detrimental impact, reducing CH4 emissions from ruminants has become a key focus for researchers worldwide, driven by the urgent need to mitigate the release of this potent greenhouse gas (Khusro et al. 2022a). Various strategies, such as altering feed consumption and using dietary additives, are being explored to curb CH4 production, presenting a promising area of study for environmental conservation and climate change mitigation efforts (Khusro et al. 2022b). In recent years, various in vitro strategies have been employed to reduce CH4 emissions from livestock, with dietary manipulation emerging as one of the most effective approaches. As global demand for meat, milk and other ruminant-derived products continue to rise, incorporating feed additives presents a promising solution to mitigate CH4 emissions (Khusro et al. 2022b). Additives, such as plant extracts, probiotics, plant metabolites, exogenous enzymes, and organic acids, can alter the gut microflora of ruminants, thereby influencing fermentation kinetics and reducing CH4 emissions (Elghandour et al. 2019). Additionally, these supplements enhance feed quality and adjust the dietary proportions, ultimately affecting gut microbial metabolism and further altering fermentation processes (Haque 2018). Previous research demonstrated that wheatgrass can enhance the growth performance and flesh quality of common carp (Barbacariu et al. 2021; Burducea et al. 2022), suggesting its potential as a feed additive for other animals, particularly ruminants. The current findings open new avenues for exploring wheatgrass as an additive to reduce CH4 emissions in livestock. PEER-REVIEWED ARTICLE bioresources.cnr.ncsu.edu Saluguti et al. (2025). “Mitigat. methanogen. in ruminant,” BioResources 20(3), 5870-5883. 5880 CONCLUSIONS 1. In summary, among the 21 selected compounds of wheatgrass, five compounds met Lipinski’s rule of five criteria. 2. In silico analysis revealed strong binding potential of these compounds with the MCR receptor, with N,N-tetramethylene-.alpha.-(aminomethylene)glutaconic anhydride showing the highest docking score of -7.3 kcal/mol using CB-Dock2 tool. The other compounds had lower binding affinities. 3. This study suggested that 2,4,6-trimethyl-1,3-phenylenediamine, Caryophyllene oxide, Caryophyllene, N,N-tetramethylene-.alpha.-(aminomethylene)glutaconic anhydride, and n-hexadecanoic acid could be promising anti-methanogenic agents in ruminants. 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