Exact Mass: 364.26268319999997
Exact Mass Matches: 364.26268319999997
Found 471 metabolites which its exact mass value is equals to given mass value 364.26268319999997,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Tetrahydrocortisone
Cortisol is a corticosteroid hormone that is involved in the response to stress; it increases blood pressure and blood sugar levels and suppresses the immune system. Synthetic cortisol, also known as hydrocortisone, is used as a drug mainly to fight allergies and inflammation. -- Wikipedia; As an oral or injectable drug, cortisol is also known as hydrocortisone. It is used as an immunosuppressive drug, given by injection in the treatment of severe allergic reactions such as anaphylaxis and angioedema, in place of prednisolone in patients who need steroid treatment but cannot take oral medication, and peri-operatively in patients on long-term steroid treatment to prevent an Addisonian crisis. -- Wikipedia [HMDB] Cortisol is a corticosteroid hormone that is involved in the response to stress; it increases blood pressure and blood sugar levels and suppresses the immune system. Synthetic cortisol, also known as hydrocortisone, is used as a drug mainly to fight allergies and inflammation. -- Wikipedia; As an oral or injectable drug, cortisol is also known as hydrocortisone. It is used as an immunosuppressive drug, given by injection in the treatment of severe allergic reactions such as anaphylaxis and angioedema, in place of prednisolone in patients who need steroid treatment but cannot take oral medication, and peri-operatively in patients on long-term steroid treatment to prevent an Addisonian crisis. -- Wikipedia. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones Tetrahydrocortisone is a stress-induced hormone. Tetrahydrocortisone is also a urinary metabolite of Cortisone derived from the reduction of Cortisone by 5-reductase[1].
Dihydrocortisol
Dihydrocortisol is the product of the enzyme steroid 5-beta-reductase (EC 1.3.1.3), which catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone, testosterone, aldosterone, corticosterone, and cortisol to 5-beta-reduced metabolites. A deficiency in this enzyme is associated with a congenital defect in bile acid synthesis (OMIM: 235555). Dihydrocortisol is the substrate of the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC 1.1.1.225, 1.1.1.213, 1.3.1.20, 1.1.1.50), and is an intermediate in bile acid biosynthesis, C21-steroid hormone metabolism, androgen and estrogen metabolism, and the metabolism of xenobiotics by cytochrome P450 (KEGG). Dihydrocortisol is the product of the enzyme Steroid 5-beta-reductase [EC 1.3.1.3], which catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone, testosterone, aldosterone, corticosterone and cortisol to 5-beta-reduced metabolites. A deficiency in this enzyme is associated with congenital defect in bile acid synthesis. (OMIM 235555) 5β-Dihydrocortisol, a metabolite of Cortisol, is a potential mineralocorticoid. 5β-Dihydrocortisol can potentiate glucocorticoid activity in raising the intraocular pressure. 5β-Dihydrocortisol causes breast cancer cell apoptosis[1][2][3][4][5].
3a,11b,21-Trihydroxy-20-oxo-5b-pregnan-18-al
3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is an intermediate in C21-Steroid hormone metabolism. 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is converted from 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al via the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC 1.1.1.50). [HMDB] 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is an intermediate in C21-Steroid hormone metabolism. 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is converted from 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al via the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC 1.1.1.50).
11b,17a,21-Trihydroxypreg-nenolone
11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1). [HMDB] 11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1).
Quinestrol
Quinestrol is only found in individuals that have used or taken this drug. It is a 3-cyclopentyl ether of ethinyl estradiol.Estrogens diffuse into their target cells and interact with a protein receptor (the estrogen receptor). Estrogen interacts with a target cell receptor. When the estrogen receptor has bound its ligand it can enter the nucleus of the target cell, and regulate gene transcription which leads to formation of messenger RNA. The mRNA interacts with ribosomes to produce specific proteins that express the effect of estradiol upon the target cell. Estrogens increase the hepatic synthesis of sex hormone binding globulin (SHBG), thyroid-binding globulin (TBG), and other serum proteins and suppress follicle-stimulating hormone (FSH) from the anterior pituitary. Target cells include the female reproductive tract, the mammary gland, the hypothalamus, and the pituitary. Estrogens increase the hepatic synthesis of sex hormone binding globulin (SHBG), thyroid-binding globulin (TBG), and other serum proteins and suppress follicle-stimulating hormone (FSH) from the anterior pituitary. The combination of an estrogen with a progestin suppresses the hypothalamic-pituitary system, decreasing the secretion of gonadotropin-releasing hormone (GnRH). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D004967 - Estrogens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C483 - Therapeutic Estrogen
7-O-Acetylaustroinulin
7-O-Acetylaustroinulin is from Stevia rebaudiana (stevia). From Stevia rebaudiana (stevia)
6-O-Acetylaustroinulin
6-O-Acetylaustroinulin is isolated from Stevia rebaudiana (stevia). Isolated from Stevia rebaudiana (stevia)
4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one
4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one is found in green vegetables. 4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one is a constituent of Centella asiatica (Asiatic pennywort)
3-Methyl-5-pentyl-2-furantridecanoic acid
3-methyl-5-pentyl-2-furantridecanoic acid is a furan fatty acid (F-acid). F-acids are heterocyclic fatty acids containing a central furan moiety with a carboxylalkyl chain (mostly 7, 9, 11, or 13 carbons) in the 2-position and an alkyl chain (mostly 3 or 5 carbons) in the 5-position. Despite being found in low concentrations in food lipids, they are excellent antixoxidants and radical scavengers. This allows them to play an important role in preventing lipid peroxidation and protecting polyunsaturated fatty acids. They are often incorporated into phospholipids and cholesterol esters of fish and other marine organisms. 3-methyl-5-pentyl-2-furantridecanoic acid, in particular, can be described by the shorthand notation 13M5. This refers to its 13-carbon carboxyalkyl moiety, the methyl substitution in the 3-position of its furan moiety, and its 5-carbon alkyl moiety.
2-Arachidonyl Glycerol ether
2-Arachidonyl glycerol ether (2-AG ether) has been isolated from porcine brain and its structure determined by mass spec analysis.1 2-AG ether has also been synthesized as an analog of the endogenous cannabinoid (CB), 2-AG, for structure activity testing.2 2-AG ether is a selective central cannabinoid (CB1) receptor agonist exhibiting Ki values of 21.2 nM and >3 ?M at the CB1 and peripheral cannabinoid (CB2) receptors, respectively, and displays the typical tetrad of CB activities in mice.1 It is much more chemically stable than 2-AG, with an endogenous half-life of hours rather than minutes.3 However, it is at least 10-fold less potent than 2-AG in eliciting typical CB1-mediated responses.2 2-AG ether elicits modest reductions in IOP in rabbits when administered at doses exceeding 50 ?g per eye.3 2-AG ether increases aqueous humor outflow via the CB1 receptor in the trabecular meshwork. [HMDB] 2-Arachidonyl glycerol ether (2-AG ether) has been isolated from porcine brain and its structure determined by mass spec analysis.1 2-AG ether has also been synthesized as an analog of the endogenous cannabinoid (CB), 2-AG, for structure activity testing.2 2-AG ether is a selective central cannabinoid (CB1) receptor agonist exhibiting Ki values of 21.2 nM and >3 µM at the CB1 and peripheral cannabinoid (CB2) receptors, respectively, and displays the typical tetrad of CB activities in mice.1 It is much more chemically stable than 2-AG, with an endogenous half-life of hours rather than minutes.3 However, it is at least 10-fold less potent than 2-AG in eliciting typical CB1-mediated responses.2 2-AG ether elicits modest reductions in IOP in rabbits when administered at doses exceeding 50 µg per eye.3 2-AG ether increases aqueous humor outflow via the CB1 receptor in the trabecular meshwork.
11b,21-Dihydroxy-3,20-oxo-5b-pregnan-18-al
DG(22:5(4Z,7Z,10Z,13Z,16Z)/16:1(9Z)/0:0) is a diglyceride, or a diacylglycerol (DAG). It is a glyceride consisting of two fatty acid chains covalently bonded to a glycerol molecule through ester linkages. Diacylglycerols can have many different combinations of fatty acids attached at both the C-1 and C-2 positions. DG(22:5(4Z,7Z,10Z,13Z,16Z)/16:1(9Z)/0:0), in particular, consists of one chain of docosapentaenoic acid at the C-1 position and one chain of palmitoleic acid at the C-2 position. The docosapentaenoic acid moiety is derived from animal fats and brain, while the palmitoleic acid moiety is derived from animal fats and vegetable oils. Mono- and diacylglycerols are common food additives used to blend together certain ingredients, such as oil and water, which would not otherwise blend well. Dacylglycerols are often found in bakery products, beverages, ice cream, chewing gum, shortening, whipped toppings, margarine, and confections. 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al is an intermediate in C21-Steroid hormone metabolism. 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al is converted from Aldosterone via the enzyme 3-oxo-5beta-steroid 4-dehydrogenase (EC:1.3.99.6). It is then converted to 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al via the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC:1.1.1.50).
18-Hydroxy-11-dehydrotetrahydrocorticosterone
18-Hydroxy-11-dehydrotetrahydrocorticosterone is a major urinary metabolite of 18-hydroxycorticosterone and is used to monitor 18-hydroxycorticosterone secretion rate. A human metabolite taken as a putative food compound of mammalian origin [HMDB]
Vanillin 3-(L-menthoxy)propane-1,2-diol acetal
Vanillin 3-(L-menthoxy)propane-1,2-diol acetal is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]") It is used as a food additive .
5-Hexyl-3,4-dimethyl-2-furanundecanoic acid
5-Hexyl-3,4-dimethyl-2-furanundecanoic acid is a furan fatty acid (F-acid). F-acids are heterocyclic fatty acids containing a central furan moiety with a carboxylalkyl chain (mostly 7, 9, 11, or 13 carbons) in the 2-position and an alkyl chain (mostly 3 or 5 carbons) in the 5-position. Despite being found in low concentrations in food lipids, they are excellent antixoxidants and radical scavengers. This allows them to play an important role in preventing lipid peroxidation and protecting polyunsaturated fatty acids. They are often incorporated into phospholipids and cholesterol esters of fish and other marine organisms. 5-Hexyl-3,4-dimethyl-2-furanundecanoic acid, in particular, can be described by the shorthand notation 11D6. This refers to its 11-carbon carboxyalkyl moiety, the dimethyl substitutions in the 3- and 4-positions of its furan moiety, and its 6-carbon alkyl moiety. It has been identified in the crayfish hepatopancreas.
5-Heptyl-3-methyl-2-furanundecanoic acid
5-Heptyl-3-methyl-2-furanundecanoic acid is a furan fatty acid (F-acid). F-acids are heterocyclic fatty acids containing a central furan moiety with a carboxylalkyl chain (mostly 7, 9, 11, or 13 carbons) in the 2-position and an alkyl chain (mostly 3 or 5 carbons) in the 5-position. Despite being found in low concentrations in food lipids, they are excellent antixoxidants and radical scavengers. This allows them to play an important role in preventing lipid peroxidation and protecting polyunsaturated fatty acids. They are often incorporated into phospholipids and cholesterol esters of fish and other marine organisms. 5-Heptyl-3-methyl-2-furanundecanoic acid, in particular, can be described by the shorthand notation 11M7. This refers to its 11-carbon carboxyalkyl moiety, the methyl substitution in the 3-position of its furan moiety, and its 7-carbon alkyl moiety. It has been identified in the crayfish hepatopancreas.
3,4-Dimethyl-5-pentyl-2-furandodecanoic acid
3,4-Dimethyl-5-pentyl-2-furandodecanoic acid is a furan fatty acid (F-acid). F-acids are heterocyclic fatty acids containing a central furan moiety with a carboxylalkyl chain (mostly 7, 9, 11, or 13 carbons) in the 2-position and an alkyl chain (mostly 3 or 5 carbons) in the 5-position. Despite being found in low concentrations in food lipids, they are excellent antixoxidants and radical scavengers. This allows them to play an important role in preventing lipid peroxidation and protecting polyunsaturated fatty acids. They are often incorporated into phospholipids and cholesterol esters of fish and other marine organisms. 3,4-Dimethyl-5-pentyl-2-furandodecanoic acid, in particular, can be described by the shorthand notation 12D5. This refers to its 12-carbon carboxyalkyl moiety, the dimethyl substitutions in the 3- and 4-positions of its furan moiety, and its 5-carbon alkyl moiety. It has been identified in the crayfish hepatopancreas.
2-[(5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoxy]propane-1,3-diol
Reichstein's substance E
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
4,5-Dihydrocortisol
Allotetrahydrocortisone
Ciprostene
Clinprost
Butyl-(2,5-dimethyl-7-(2,4,6-trimethylphenyl)-7H-pyrrolo(2,3-d)pyrimidin-4-yl)ethylamine
Fallypride
C20H29FN2O3 (364.21620959999996)
2-Icosa-5,8,11,14-tetraen-2-yloxypropane-1,3-diol
Tenacigenin B
Tetrahydroaldosterone
3-Icosa-5,8,11,14-tetraen-2-yloxypropane-1,2-diol
Methyl-[10]-gingerol
Methyl-[10]-gingerol is a member of the class of compounds known as dimethoxybenzenes. Dimethoxybenzenes are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups. Methyl-[10]-gingerol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Methyl-[10]-gingerol can be found in ginger, which makes methyl-[10]-gingerol a potential biomarker for the consumption of this food product.
Methyl 15-hydroxy-8alpha,12alpha-epidioxiabiet-13-en-19-oate
9-oxo-15S-Hydroxy-prosta-10,13E-dien-1-oic acid, ethyl ester
Ciprostene
C78568 - Prostaglandin Analogue
2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-methoxy-5-(2-phenylethyl)phenol
(3beta,16alpha)-phyllocladane-3,16,17-triol 17-acetate
Tenacigenin B
2,5-dimethoxy-3-methyl-6-tridecylcyclohexa-2,5-diene-1,4-dione
(-)-(3alpha,17alpha,20(S))-3,17,20-trihydroxypregnane-6,16-dione|(-)-<3alpha,17alpha,20(S)>-3,17,20-trihydroxypregnane-6,16-dione
(3S,5S,8R,9R,10S)-3-acetoxy-9,13-epoxy-16-norlabda-13E-en-15-oic acid|negundoin B
14-(Z)-coumaroxy-(1E,4E,8E)-4,8,11,11-tetramethylcycloundeca-1,4,8-triene|14-hydroxy-alpha-humulene (Z)-coumaric acid ester
(18S,19S)-19-deoxo-4-hydroxy-18,19-dimethoxydictyolactone
2,3-Dihydro-3-hydroxy-5-oxo-5-deoxyprotomycinolide IV
methyl 7alpha-hydroxy-8beta,14beta-dioxopodocarpan-13beta-oate
(-)-9alpha-acetoxy-2beta,13beta-dihydroxyverrucosane
Me ester -(ent-6alpha,7beta,13E)-6,7-Dihydroxy-2-oxo-3,13-clerodadien-15-oic acid
Labd-8(20)-ene-15,18-dioic acid, dimethyl ester, (13R)-
16-Ac-(8alpha,12R,13E)-8,12-Epoxy-13-labdene-15,16-diol
14-Ac-(17R)-8,10,13(15)-Lobatriene-14,17,18-triol|Loba-8,10,13(15)-trien-14,17,18-triol-14-acetat|loba-8,10,13(15)-triene-14,17,18-triol 14 acetate
(22E)-24,26-cyclo-19-norcholesta-1,3,5(10),22-tetraen-3-ol
A 3-hydroxy steroid that is 24,26-cyclo-19-norcholesta-1,3,5(10),22-tetraene substituted by a hydroxy group at position 3. It is isolated from the Hainan soft coral Dendronephthya studeri.
(2R)-5-(2-acetoxytridecyl)resorcinol methylether|5-(2-acetoxytridecyl)-3-methoxyphenol
1-hydroxy-5-hydroxymethyl-6-methoxymethyl-3-methoxy-2-(7-methoxy-3,7-dimethylocta-2,6-dienyl)benzene|hericenol D
16-Hydroxy,6-Ac-(1R,3E,6R,7E,11R,12R)-3,7-Dolabelladiene-6,12-diol
12-acetoxy-8alpha,13-dihydroxylabd-14-en-7-one|curcumrinol C
2alpha,3beta,4beta,18-tetrahydroxypregn-5-en-16-one
3beta,14beta,15alpha,16alpha-hydroxy-20-oxo-Delta5-pregnene-tetraol
(1R,2E,4R,5R,7E,10S,11S,12R)-5-acetoxy-10,18-dihydroxy-2,7-dolabelladiene
8beta-H-Ent-labda-13-(E)-en-15,17-disaeuredimethylester|8beta-H-Ent-labda-13-(Z)-en-15,17-disaeuredimethylester
(2E,6Z,10E,12R)-7-[(acetyloxy)methyl]-3,11,15-trimethylhexadeca-2,6,10,14-tetraene-1,12-diol
(1S*,3E,11S*,12S*)-9-acetoxy-7,8-epoxydolabella-3-en-12-ol
8beta(17)-epoxy-15,15-dimethoxylabd-12(E)-en-16-al|aframolin B
4(5)-dihydrokolevan-12-en-16-acetoxy-15-oic acid|ajugalaevigatic acid|cleroda-12-en-16-acetoxy-15-oic acid
(16R)-6-hydroxy-16beta-(methoxymethyl)-15-oxo-6,7-seco-ent-kauran-7,20-olide|(1R,2R,4aS,7R,8S,9aS)-5,6,7,8-tetrahydro-2-(hydroxymethyl)-8-(methoxymethyl)-3,3-dimethylspiro[cyclohexane-1,4-[2]oxa[7,9a]methanocyclohepta[c]pyran]-1,9(4aH)-dione|sculponeatin O
(1R,3R,4R,13R,14R,15S,7E,11E)-13-hydroxy-17-methoxy-3,4-epoxycembra-7,11-dien-16,14-olide|durumolide Q
(1R*,3R*,4S*,14S*,15S*,7E,11E)-18-hydroxy-17-methoxy-3,4-epoxycembra-7,11-dien-16,14-olide|durumolide P
4,13beta-dihydroxy-14-oxo-3,4-secoatis-16-en-3-oic acid methyl ester
3beta,14beta,20-trihydroxy-5beta-pregn-18-carboxylic acid-20-lactone
7-acetyldistanol|ent-7alpha-acetoxy-16beta,18-dihydroxy-kaurane
16-oxo-2,3-secoandrostan-2,3-dioic acid dimethyl ester
3alpha,15alpha,21-Trihydroxy-5alpha-pregnandion-(11,20)
2,4-Dihydroxy-6-methoxy-3-(3-methyl-2-butenyl)-5-(1-ethoxy-3-methylbutyl)acetophenone
7alpha,14beta-dihydroxy-16beta-methoxymethyl-ent-kaur-3,15-dione|glaucocalyxin I
methyl 11-(3,4-dimethyl-5-pentylfuran-2-yl)undecanoate
(20S*)-1alpha,14beta,15beta-trihydroxy-20-methoxy-7alpha,20-epoxy-ent-kaur-16-ene|rubluanin B
21-Me ether-(3alpha,5alpha,11beta)-3,11,21-Trihydroxypregnan-20-one
11-Ac-(ent-11beta,15()-4(18)-erythroxylene-11,15,16-triol|11-Ac-(ent-11beta,15xi)-4(18)-erythroxylene-11,15,16-triol|ent-11beta-acetoxydolabr-4(18)-en-15xi,16-diol
(3aS,7S,9aS)-3a,5,6,7,9,9a-hexahydro-7,9a-dihydroxy-1-(7-hydroxy-6-methylheptan-2-yl)-3a-methylcyclopenta[b]chromen-8(3H)-one|TCA E
6beta-hydroxy-15alpha-methoxy-9alpha,13,15,16-bis-epoxylabdan-7-one
6beta-Acetoxy-8beta-hydroxy-ent-13E-labden-15-saeure; Acetyl-laurofolic acid
3-Ac-15-Isopimarene-3beta,7beta,8beta-triol|3beta-acetoxy-15-isopimarene-7beta,8beta-diol
(3R)-8-hydroxy-6-methoxy-3-(11-hydroxyundecyl)-3,4-dihydroisocoumarin
(+)-polyanthelin A|(+)-polyanthellin A|polyanthelin A
methyl 15,17-epoxy-17alpha-methoxy-ent-isocopalan-16-oate
agallochin N|methyl ent-13-epi-8,13-epoxy-2,3-secolabd-14-en-2,11-olid-3-oate
(15S)-7,8,16-trihydroxyserrulatan-19-oate|methyl (15S)-7,8,16-trihydroxyserrulatan-19-oate
ent-isopimaran-8beta-hydroxy-15R,16-acetonide|forrestin J
6alpha-(3-methylvaleryloxy)-1-hydroxy-4alphaH-1,10-secoeudesma-5(10),11(13)-dien-12,8beta-olide
(13R)-6beta-acetoxy-labda-8,14-diene-7beta,13-diol|6beta-acetoxy-7beta,13-dihydroxy-labda-8,14-diene
6alpha,7alpha-dihydroxy-15-methoxycleroda-3,13-dien-16,15-olide|ptycho-6alpha,7alpha-diol
3,4-Dihydro-8-hydroxy-6-methoxy-3-(6-hydroxyundecyl)-1H-2-benzopyran-1-one
(1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20 acetate
16alpha,17-dihydroxy-15-oxo-ent-kaur-19-oic acid methyl ester|16??,17-Dihydroxy-15-oxo-ent-kaur-19-oic acid methyl ester
11-Ac-(ent-5alpha,11beta,15xi)-1-Rosene-11,15,16-triol|ent-11beta-acetoxy-5alpha-ros-1(10)-en-15xi,16-diol
methyl-14-O-(2-methylbutyryl)-oxyphylloate|methyl-14-O-<2-methylbutyryl>-oxyphylloate
(1S,3Z,7S,11S,12S)-(+)-verticilla-3,8(19)-dien-7,12,20-triol 20-acetate
(4R,6R)-dihydroxy-4-(10(Z)-heptadecenyl)-2-cyclohexenone
(betaxi,1S,2R,4aR,7S,8aR)-7-acetyloxy-1,2,3,4,4a,7,8,8a-octahydro-beta,1,2,4a,5-pentamethylnaphthalene-1-pentanoic acid|2beta-(acetyloxy)clerod-3-en-15-oic acid
THE
CONFIDENCE standard compound; INTERNAL_ID 1214
[12-hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienyl] acetate
Tetrahydrocortisone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones Tetrahydrocortisone is a stress-induced hormone. Tetrahydrocortisone is also a urinary metabolite of Cortisone derived from the reduction of Cortisone by 5-reductase[1].
5-[(1S,2R,4aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid
[12-hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienyl] acetate
[12-hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienyl] acetate [IIN-based: Match]
[12-hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienyl] acetate_major
5-[(1S,2R,4aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid_major
2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-methoxy-5-(2-phenylethyl)phenol_major
11-deoxy-16,16-dimethyl-PGE2
Carbaprostacyclin methyl ester
Vanillin 3-(L-menthoxy)propane-1,2-diol acetal
6-O-Acetylaustroinulin
7-O-Acetylaustroinulin
Quinestrol
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D004967 - Estrogens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C483 - Therapeutic Estrogen
Urocortisone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones Tetrahydrocortisone is a stress-induced hormone. Tetrahydrocortisone is also a urinary metabolite of Cortisone derived from the reduction of Cortisone by 5-reductase[1].
ST 21:2;O5
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Hydrallostane
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
trans,trans-4-(4-ethoxy-2,3-difluoro-phenyl)-4-propyl-bicyclohexyl
C23H34F2O (364.25775780000004)
Tetrahydroaldosterone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
(RAC-TRANS)-1-TERT-BUTYL 3-METHYL 4-(5,6-DIMETHOXYPYRIDIN-2-YL)PYRROLIDINE-1,3-DICARBOXYLATE
4,4-(1,3,4-oxadiazole-2,5-diyl)bis[N,N-diethylaniline]
4-Methylphenyl trans-4-(4-pentylcyclohexyl)benzoate
(S)-3-aminomethyl-N,N-diethyl-5-methylhexanamide D-(-)-tartrate
C4H6O6*C12H26N2O (364.22094020000003)
Methyl (13E)-16-hydroxy-16-methyl-9-oxoprosta-8(12),13-dien-1-oate
2-Benzyl-2-dimethylamino-1-(4-piperidinylphenyl)-1-butanone
C24H32N2O (364.25145019999997)
2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro[5.1.11.2]-henicosan-21-one
Fallypride
C20H29FN2O3 (364.21620959999996)
D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists
5-(3-Fluoropropyl)-2,3-dimethoxy-N-[[1-(2-propen-1-yl)-2-pyrrolidinyl]methyl]benzamide
C20H29FN2O3 (364.21620959999996)
4-((4-((((1R,2S)-2-Phenylcyclopropyl)amino)methyl)piperidin-1-yl)methyl)benzoic acid
methyl 5-[(3aS,5R,6R,6aS)-5-hydroxy-6-[(E,3R)-3-hydroxyoct-1-enyl]-1,3a,4,5,6,6a-hexahydropentalen-2-yl]pentanoate
2-(3,7-Dimethylocta-2,6-dienyl)-3-methoxy-5-(2-phenylethyl)phenol
3a,11b,21-Trihydroxy-20-oxo-5b-pregnan-18-al
3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is an intermediate in C21-Steroid hormone metabolism. 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is converted from 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al via the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC 1.1.1.50). [HMDB] 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is an intermediate in C21-Steroid hormone metabolism. 3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al is converted from 11beta,21-Dihydroxy-3,20-oxo-5beta-pregnan-18-al via the enzyme 3-alpha-hydroxysteroid dehydrogenase (EC 1.1.1.50).
11b,17a,21-Trihydroxypreg-nenolone
11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1). [HMDB] 11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1).
(1E,3R,4R,10R,11S)-4,9,14-trihydroxy-14-(methoxymethyl)-4,10-dimethyl-6-propan-2-yltricyclo[9.3.0.03,7]tetradeca-1,6-dien-5-one
3(N,N-Dimethylmyristylammonio)propanesulfonate
C19H42NO3S+ (364.2885242000001)
(3R,5R,8S,9S,10S,14S)-3,11-dihydroxy-17-(2-hydroxyacetyl)-10-methyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-13-carbaldehyde
2-[(5E,8E,11E,14E)-icosa-5,8,11,14-tetraenoxy]propane-1,3-diol
methyl 5-[5-hydroxy-6-[(E)-3-hydroxyoct-1-enyl]-1,3a,4,5,6,6a-hexahydropentalen-2-yl]pentanoate
(5E)-5-[5-hydroxy-4-[(E)-3-hydroxyoct-1-enyl]-6a-methyl-1,3,3a,4,5,6-hexahydropentalen-2-ylidene]pentanoic acid
3,5-Dihydroxy-2,6,6,10,14-pentamethyl-11,13-dioxatetracyclo[8.8.0.02,7.012,17]octadec-12(17)-en-16-one
1-[(8S,9S,10R)-10-(hydroxymethyl)-9-(4-phenylphenyl)-1,6-diazabicyclo[6.2.0]decan-6-yl]ethanone
1-[(8R,9S,10R)-10-(hydroxymethyl)-9-(4-phenylphenyl)-1,6-diazabicyclo[6.2.0]decan-6-yl]ethanone
2-[(3E)-hexadec-3-enoyl]-3,5-dihydroxycyclohex-2-en-1-one
4-[[(9Z,12Z)-octadeca-9,12-dienoyl]amino]butanoate
(2Z,6Z,10Z)-6-(acetyloxymethyl)-12-hydroxy-10-methyl-2-(3-methylbut-3-enyl)dodeca-2,6,10-trienoic acid
7-[5-(Dimethylamino)pentylamino]-2,6,9-trimethyl-13-oxatetracyclo[6.3.1.16,9.01,5]tridecan-11-ol
N-[(2S)-butan-2-yl]-4-[(1-phenylcyclopentanecarbonyl)amino]benzamide
[1-[(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoxy]-3-hydroxypropan-2-yl] propanoate
(6E,10E)-1-Acetoxy-14-(1-hydroxy-1-methylethyl)-2,3-epoxy-3,7,11-trimethylcyclotetradecadiene
(1-acetyloxy-3-hydroxypropan-2-yl) (4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoate
2-(Ethoxycarbonyl)-3-[1-(benzyloxy)ethyl]heptanoic acid ethyl ester
2-[(11Z,14Z,17Z)-icosa-11,14,17-trienoyl]oxyacetic acid
Dihydrocortisol
5β-Dihydrocortisol, a metabolite of Cortisol, is a potential mineralocorticoid. 5β-Dihydrocortisol can potentiate glucocorticoid activity in raising the intraocular pressure. 5β-Dihydrocortisol causes breast cancer cell apoptosis[1][2][3][4][5].
3alpha,11beta,21-Trihydroxy-20-oxo-5beta-pregnan-18-al
3,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-11-one
2-hydroxy-1-[(17R)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone
20beta-dihydrocortisol
A 17alpha-hydroxy-C21-steroid that is cortisol in which the 20-oxo group has been reduced to a hydroxy group. It is a metabolite of cortisol identified in the urine of horses and humans, and its urinary excretion is increased in obesity.
9-oxo-15R-hydroxy-16,16-dimethyl-5Z,13E-prostadienoic acid
18-Hydroxy-11-dehydrotetrahydrocorticosterone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
3,5-dihydroxy-2-(1-oxo-3-hexadecenyl)-2-cyclohexene-1-one
A polyketide that consists of cyclohex-2-en-1-one substituted by hydroxy groups at positions 3 and 5 and a hexadec-3-enoyl group at position 2 (the 3E stereoisomer). It is isolated form the leaves of Virola sebifera an exhibits cytotoxic activity against human tumour cells.
2-Arachidonyl glyceryl ether
A monoalkylglycerol that is glycerol which is substituted by a (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraen-1-yl group at position 2.
DG(18:4)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
DG(19:4)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
VU0469650
VU0469650 is a potent, selective and CNS-penetrated negative allosteric modulator of mGlu1 receptor, with an IC50 of 99 nM[1].