Exact Mass: 484.35121879999997

C28H44N4O3 (484.34132339999996)

5-Carbamimidamido-2-[(1-hydroxydocosa-4,7,10,13,16,19-hexaen-1-ylidene)amino]pentanoate

N-docosahexaenoyl arginine 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 Docosahexaenoyl amide of Arginine. 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-Docosahexaenoyl Arginine 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-Docosahexaenoyl Arginine is therefore classified as a very 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.

2,6-Ditert-butyl-4-[3-(3,5-ditert-butyl-4-hydroxyphenoxy)propoxy]phenol

2,6-di-tert-butyl-4-[3-(3,5-di-tert-butyl-4-hydroxyphenoxy)propoxy]phenol

Dehydrotumulosic acid

2-{5,13-dihydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl}-6-methyl-5-methylideneheptanoic acid

dehydrotumulosic acid

(2R)-2-[(3S,10S,13R,14R,16R,17R)-3,16-dihydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoic acid

Dehydrotumulosic acid is one of the effective constituents of Poria cocos. Poria cocos, a popular Chinese medicinal herb of fungal origin, has been included in many combinations with other CM herbs for its traditionally claimed activities of inducing diuresis, excreting dampness, invigorating the spleen and tranquilizing the mind and its modern pharmacological use of modulating the immune system of the body[1]. Dehydrotumulosic acid is one of the effective constituents of Poria cocos. Poria cocos, a popular Chinese medicinal herb of fungal origin, has been included in many combinations with other CM herbs for its traditionally claimed activities of inducing diuresis, excreting dampness, invigorating the spleen and tranquilizing the mind and its modern pharmacological use of modulating the immune system of the body[1].

Dehydrotumulosic

(2R)-2-[(3S,10S,13R,14R,16R,17R)-3,16-dihydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoic acid

Cimicidanol

Sootepin D

methyl 3-[(1S,4R,5R,8S,9S,12R,13R)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(E,2R)-6-methyl-7-oxohept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate

Sootepin D is a natural product found in Gardenia sootepensis with data available.

Fomefficinic acid B

(+)-Fomefficinic acid B

Garcihombronane J

Poricoic acid B

(2R)-2-[(2R,3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-2-hydroxy-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,7,8-hexahydrocyclopenta[a]naphthalen-3-yl]-6-methylhept-5-enoic acid

A pentacyclic triterpenoid with formula C31H48O4, originally isolated from the roots of Tripterygium regelii.

24(E)-3,4-Secodammara-4(28),20,24-trien-3,26-dioic acid-3-methylester|methyl (24E)-3,4-secodammara-4(28),20,24-trien-26-oic acid-3-oate|methyl (24E)-3,4-secodammara-4(28),20,24-triene-26-oic acid-3-oate

22beta-hydroxy-3-oxo-olean-12-en-28-oic acid methyl ester|22beta-Hydroxy-3-oxo-olean-12-en-28-saeure-methylester|methyl 22beta-hydroxy-3-oxo-olean-12-en-28-ate|methyl 22beta-hydroxy-3-oxoolean-12-en-28-oate|methyl 22beta-hydroxy-3-oxoolean-12-en-28-onate

22beta-hydroxy-3-oxo-olean-12-en-28-oic acid methyl ester|22beta-Hydroxy-3-oxo-olean-12-en-28-saeure-methylester|methyl 22beta-hydroxy-3-oxo-olean-12-en-28-ate|methyl 22beta-hydroxy-3-oxoolean-12-en-28-oate|methyl 22beta-hydroxy-3-oxoolean-12-en-28-onate

(23R,24S)-5alpha-cholestane-3beta,4beta,6beta,8,15beta-23,24-heptaol

lamesticumin E

Soyasapogenol G

11-oxo-beta-boswellic acid methyl ester|3alpha-hydroxy-11-oxo-urs-12-en-24-oic acid methyl ester|3alpha-hydroxy-11-oxo-ursen-(12)-oic acid-(24)-methyl ester|3alpha-Hydroxy-11-oxo-ursen-(12)-saeure-(24)-methylester|methyl 3-alpha-hydroxy-11-oxours-12-en-24-oate|methyl 3alpha-hydroxy-11-oxours-12-en-24-oate

11-oxo-beta-boswellic acid methyl ester|3alpha-hydroxy-11-oxo-urs-12-en-24-oic acid methyl ester|3alpha-hydroxy-11-oxo-ursen-(12)-oic acid-(24)-methyl ester|3alpha-Hydroxy-11-oxo-ursen-(12)-saeure-(24)-methylester|methyl 3-alpha-hydroxy-11-oxours-12-en-24-oate|methyl 3alpha-hydroxy-11-oxours-12-en-24-oate

(5E,6Z,8Z)-(1S,3R)-9,10-seco-5(10),6,8-cholestatrien-1,3-diethanoate

D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols

(5Z,7E)-(1S,3R,20R,22R)-26,27-dimethyl-24a,24b-dihomo-9,10-seco-5,7,10(19)-cholestatrien-23-yne-1,3,22,25-tetrol

A pyranone diterpenoid isolated from Nalanthamala and Chaunopycnis alba and has been shown to be a blocker of the voltage-gated potassium channel Kv1.3

Regelin C

4-Apo-beta-carotenol

C35H48O (484.37049579999996)

18alpha-Glycyrrhetic Acid Methyl Ester

Gypsogenate

C30H44O5-2 (484.3188574)

A natural product found in Melia toosendan.

Gypsogenate(2-)

C30H44O5-2 (484.3188574)

Hainanic acid A

A pentacyclic triterpenoid with formula C30H44O5, originally isolated from the bark of Tripterygium wilfordii.

Gypsogenate(2-)

A dicarboxylic acid dianion obtained by deprotonation of both carboxy groups of gypsogenic acid; major species at pH 7.3.

N-t-Boc-deacetyl-leupeptin

N-tert-Butyloxycarbonyl-deacetyl-leupeptin

C23H44N6O5 (484.3373014)

(25S)-5alpha-cholestan-3beta,4beta,6alpha,8beta,15alpha,16beta,26-heptol

(25S)-5alpha-cholestan-3beta,6alpha,7beta,8beta,15alpha,16beta,26-heptol

TG(25:0)

TG(4:0_6:0_15:0)

C28H52O6 (484.3763692)

DG(28:7)

DG(18:3(1)_10:4)

24(e)-3,4-secodammara-4(28),20,24-trien-3,26-dioicacid-3-methylester

{"Ingredient_id": "HBIN004375","Ingredient_name": "24(e)-3,4-secodammara-4(28),20,24-trien-3,26-dioicacid-3-methylester","Alias": "NA","Ingredient_formula": "C31H48O4","Ingredient_Smile": "CC(=C)C1CCC2(C(C1(C)CCC(=O)OC)CCC3C2(CCC3C(=C)CCC=C(C)C(=O)O)C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "19595","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

5α-cholest-3β,6α,7α,8β,15α,16β,26-sevol

{"Ingredient_id": "HBIN011409","Ingredient_name": "5\u03b1-cholest-3\u03b2,6\u03b1,7\u03b1,8\u03b2,15\u03b1,16\u03b2,26-sevol","Alias": "NA","Ingredient_formula": "C27H48O7","Ingredient_Smile": "CC(CCCC(C)C1C(C(C2C1(CCC3C2(C(C(C4C3(CCC(C4)O)C)O)O)O)C)O)O)CO","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "3587","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

6α-hydroxylup-20(29)-en-3-oxo-28-oicacid

(2e)-n-[(1s,3as,3bs,5ar,6r,9ar,9bs,11as)-6-(acetyloxy)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,5h,5ah,6h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]-2-methylbut-2-enimidic acid

C30H48N2O3 (484.3664738)

(3r,3as,5ar,5br,7r,7ar,9s,11ar,11br,13r,13ar,13bs)-9,13-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-7-yl acetate

(1r,3r,3as,3bs,5r,5as,6r,7s,9as,9br,11ar)-1-[(2r,4r,5s)-4,5-dihydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-3,3b,5,6,7-pentol

n-[(3as,3br,5ar,6r,7s,9ar,9bs,11as)-6-(acetyloxy)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-3h,3ah,3bh,4h,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]-3-methylbut-2-enimidic acid

n-[(3as,3br,5ar,6r,7s,9ar,9bs,11as)-6-(acetyloxy)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-3h,3ah,3bh,4h,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]-3-methylbut-2-enimidic acid

n-[(3as,3br,5as,7r,8s,9as,9bs,11as)-8-(acetyloxy)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-3h,3ah,3bh,4h,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]-3-methylbut-2-enimidic acid