Exact Mass: 431.324671

Exact Mass Matches: 431.324671

Found 121 metabolites which its exact mass value is equals to given mass value 431.324671, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Peimine

(3S,4aS,5S,6aS,6bS,8aS,9S,9aS,12S,15aS,15bR,16aS,16bR)-9,12,16b-Trimethyltetracosahydrobenzo[4,5]indeno[1,2-h]pyrido[1,2-b]isoquinoline-3,5,9-triol

C27H45NO3 (431.339926)

Verticine is an alkaloid. Peimine is a natural product found in Fritillaria anhuiensis, Fritillaria cirrhosa, and other organisms with data available. D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents > D014704 - Veratrum Alkaloids Peimine (Verticine) is a natural compound with excellent anti-inflammatory activity. Peimine (Verticine) is a natural compound with excellent anti-inflammatory activity.

Zhebeinine

C27H45NO3 (431.339926)

D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents > D014704 - Veratrum Alkaloids

Solanocardinol

10,14,16,20-tetramethyl-23-oxa-18-azahexacyclo[12.11.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁴.0¹⁷,²²]pentacosane-7,22-diol

C27H45NO3 (431.339926)

22-Isopimpifolidine is found in garden tomato. 22-Isopimpifolidine is an alkaloid from roots of Lycopersicon pimpinellifolium (currant tomato). Alkaloid from roots of Lycopersicon pimpinellifolium (currant tomato). 22-Isopimpifolidine is found in garden tomato.

N-Stearoyl phenylalanine

(2S)-2-[(1-hydroxyoctadecylidene)amino]-3-phenylpropanoic acid

C27H45NO3 (431.339926)

N-stearoyl phenylalanine belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Stearic acid amide of Phenylalanine. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Stearoyl phenylalanine is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Stearoyl phenylalanine is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

Aglepristone

17-[4-(dimethylamino)phenyl]-14-hydroxy-15-methyl-14-(prop-1-en-1-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1,6-dien-5-one

C29H37NO2 (431.2824142)

Peimine

6,10,23-trimethyl-4-azahexacyclo[12.11.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁴.0¹⁸,²³]pentacosane-10,17,20-triol

C27H45NO3 (431.339926)

Korseveriline

(1S,2R,6R,9S,10R,11S,14R,15R,17R,18S,20R,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-14,17,20-triol

C27H45NO3 (431.339926)

Origin: Plant; SubCategory_DNP: Steroidal alkaloids, Cevanine alkaloids

(20R,22S,25R)-5alpha-cevane-3alpha,6beta,7alpha-triol|3alpha-puqiedin-7-ol

C27H45NO3 (431.339926)

(3beta,5alpha,6beta)-3,5,6-Solanidanetriol

C27H45NO3 (431.339926)

AC1LB2KU

C27H45NO3 (431.339926)

Paniculidine

C27H45NO3 (431.339926)

18-phenethylaminoavarone|3-phenethylaminoavarone

C29H37NO2 (431.2824142)

Baikeine

C27H45NO3 (431.339926)

lipocarbazole A2

C30H41NO (431.31879760000004)

9.alpha.-3,22-Dihydroxy-dihydrosolasodine

C27H45NO3 (431.339926)

(14S)-pellasoren|pellasoren A

C26H41NO4 (431.30354260000007)

dysidaminone G

C29H37NO2 (431.2824142)

dysidaminone M

C29H37NO2 (431.2824142)

Malyngamide H

C26H41NO4 (431.30354260000007)

2alpha-Hydroxysoladulcidine

C27H45NO3 (431.339926)

hexahydrobrachystamide-D|tetrahydrobrachystamide-E

C27H45NO3 (431.339926)

Isojuripidine

C27H45NO3 (431.339926)

17-oxo-3-benzoylbuxadine

C29H37NO2 (431.2824142)

1-oleyl ester of 3-(N-phenylamino)-1,2-propanediol|1-oleyl MPAP|2-hydroxy-3-(N-phenylamino)propyl oleate|3-phenylamino-1,2-propanediol 1-mono-oleoyl ester|3-phenylamino-1,2-propanediol monooleylester

C27H45NO3 (431.339926)

OMDM-2

(R)-N-(1-(4-hydroxyphenyl)-2-hydroxyethyl)oleamide

C27H45NO3 (431.339926)

26-amino-furostanol

C27H45NO3 (431.339926)

Isopeimine

(1R,2S,6S,9S,10S,11S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol

C27H45NO3 (431.339926)

Isoverticine is a natural product found in Fritillaria anhuiensis, Fritillaria thunbergii, and Fritillaria ebeiensis with data available. Isoverticine, a bioactive isosteroidal alkaloid isolated from bulbus of Fritillaria pallidiflora, displays significant cytotoxicity[1]. Isoverticine, a bioactive isosteroidal alkaloid isolated from bulbus of Fritillaria pallidiflora, displays significant cytotoxicity[1].

Pellasoren A

C26H41NO4 (431.30354260000007)

(E,2S,3R,4R,5S)-2-acetamido-3,4,5,14-tetrahydroxyicos-6-enoic acid

NCGC00381188-01!(E,2S,3R,4R,5S)-2-acetamido-3,4,5,14-tetrahydroxyicos-6-enoic acid

C22H41NO7 (431.28828760000005)

3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid

NCGC00381174-01!3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid

C22H41NO7 (431.28828760000005)

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid

NCGC00347750-02!(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid

C22H41NO7 (431.28828760000005)

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid

C22H41NO7 (431.28828760000005)

Isoverticine

C27H45NO3 (431.339926)

Origin: Plant; SubCategory_DNP: Steroidal alkaloids, Veratrum alkaloids Isoverticine, a bioactive isosteroidal alkaloid isolated from bulbus of Fritillaria pallidiflora, displays significant cytotoxicity[1]. Isoverticine, a bioactive isosteroidal alkaloid isolated from bulbus of Fritillaria pallidiflora, displays significant cytotoxicity[1].

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid [IIN-based on: CCMSLIB00000847931]

NCGC00347750-02!(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid [IIN-based on: CCMSLIB00000847931]

C22H41NO7 (431.28828760000005)

3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid [IIN-based on: CCMSLIB00000848436]

NCGC00381174-01!3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid [IIN-based on: CCMSLIB00000848436]

C22H41NO7 (431.28828760000005)

3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid [IIN-based: Match]

NCGC00381174-01!3-hydroxy-2-[[3-(3-hydroxy-6-methyloctanoyl)oxy-8-methylnonanoyl]amino]propanoic acid [IIN-based: Match]

C22H41NO7 (431.28828760000005)

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid [IIN-based: Match]

NCGC00347750-02!(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid [IIN-based: Match]

C22H41NO7 (431.28828760000005)

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid_major

C22H41NO7 (431.28828760000005)

(E,2S,3R,4R,5S)-4-acetyloxy-2-amino-3,5,14-trihydroxyicos-6-enoic acid_97.3\\%

C22H41NO7 (431.28828760000005)

OMDM-1

(S)-N-(1-(4-hydroxyphenyl)-2-hydroxyethyl)oleamide

C27H45NO3 (431.339926)

Sphingofungin A

2S-guanidino-3R,4R,5S,14R-tetrahydroxyicos-6E-enoic acid

C21H41N3O6 (431.29952060000005)

Sphingofungin C

2S-amino-5S-acetoxy-3R,4R,14R-trihydroxyeicos-6E-enoic acid

C22H41NO7 (431.28828760000005)

Sphingofungin D

2S-acetamido-3R,4R,5S,14R-tetrahydroxyeicos-6E-enoic acid

C22H41NO7 (431.28828760000005)

N-stearoyl phenylalanine

N-octadecanoyl-phenylalanine

C27H45NO3 (431.339926)

Pimpifolidine

10,14,16,20-tetramethyl-23-oxa-18-azahexacyclo[12.11.0.0^{2,11}.0^{5,10}.0^{15,24}.0^{17,22}]pentacosane-7,22-diol

C27H45NO3 (431.339926)

NA 27:5;O2

N-(9Z-octadecenoyl) 3,4-dimethoxybenzylamine

C27H45NO3 (431.339926)

Tris(4-tert-butylphenyl)sulfoniumperfluoro-1-butanesulfonate

C30H39S+ (431.2772314)

triethanolamine oleate

C24H49NO5 (431.36105440000006)

Octafonium chloride

C27H42ClNO (431.29547520000006)

1-[(2R)-2-amino-3-(4-fluorophenyl)propanoyl]-N-tert-butyl-4-cyclo hexyl-piperidine-4-carboxamide

C25H38FN3O2 (431.29479)

methyl 4-(octadecylcarbamoyl)benzoate

C27H45NO3 (431.339926)

Aglepristone

C29H37NO2 (431.2824142)

C147908 - Hormone Therapy Agent > C547 - Hormone Antagonist > C1891 - Progesterone Antagonist

Dodecyltriphenylphosphonium

C30H40P+ (431.28674700000005)

1,5-Anhydro-2-C-(carboxymethyl-N-hydroxyamide)-2-deoxy-3-O-myristoyl-D-glucitol

C22H41NO7 (431.28828760000005)

4,4-Diaponeurosporenoate

C30H39O2- (431.29498939999996)

A monocarboxylic acid anion that is the conjugate base of 4,4-diaponeurosporenoic acid, obtained by deprotonation of the carboxy group. Major structure at pH 7.3.