Exact Mass: 304.2038338

Exact Mass Matches: 304.2038338

Found 221 metabolites which its exact mass value is equals to given mass value 304.2038338, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

7a-Hydroxytestosterone

(7R,8R,9S,10R,13S,14R,17S)-7,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O3 (304.2038338)


4-Hydroxytestosterone is the 17-hydroxylated analog to formestane. It is commercially available on the internet as anabolic steroid for oral self-administration and does not have any therapeutic indication. Hence, only little information is available about its metabolism. So far, most studies dealt with 4-hydroxytestosterone as metabolite of formestane while one study investigated the glucuronic acid conjugates of metabolic products of 4-hydroxytestosterone. This substance is prohibited in sports by the World Anti-Doping Agency; there is to a considerable increase of structurally related steroids with anabolic effects offered via the internet. 4-Hydroxytestosterone is a metabolite of the steroidal aromatase inhibitor 4-hydroxyandrost-4-ene-3,17-dione (4OHA). (PMID: 17724580, 17610244, 17207827, 1284430) [HMDB] 4-Hydroxytestosterone is the 17-hydroxylated analog to formestane. It is commercially available on the internet as anabolic steroid for oral self-administration and does not have any therapeutic indication. Hence, only little information is available about its metabolism. So far, most studies dealt with 4-hydroxytestosterone as metabolite of formestane while one study investigated the glucuronic acid conjugates of metabolic products of 4-hydroxytestosterone. This substance is prohibited in sports by the World Anti-Doping Agency; there is to a considerable increase of structurally related steroids with anabolic effects offered via the internet. 4-Hydroxytestosterone is a metabolite of the steroidal aromatase inhibitor 4-hydroxyandrost-4-ene-3,17-dione (4OHA). (PMID: 17724580, 17610244, 17207827, 1284430).

   

11-Ketoetiocholanolone

(1S,2S,5R,7R,10S,11S,15S)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-14,17-dione

C19H28O3 (304.2038338)


11-Ketoetiocholanolone is an endogenous anabolic androgenic steroid. The concentration ratio of 11-hydroxyetiocholanolone/11-hydroxyandrosterone is increased in patients with uterine leiomyomas, and it appears to be caused by a decrease in patients metabolite of steroids. The concentration of 11-Ketoetiocholanolone is significantly higher in these patients. There is a relationship between urinary endogenous steroid metabolites and lower urinary tract function related to the residual vol. in uroflowmetry in postmenopausal women. (PMID: 15808004, 14698830, 12728469) [HMDB] 11-Ketoetiocholanolone is an endogenous anabolic androgenic steroid. The concentration ratio of 11-hydroxyetiocholanolone/11-hydroxyandrosterone is increased in patients with uterine leiomyomas, and it appears to be caused by a decrease in patients metabolite of steroids. The concentration of 11-Ketoetiocholanolone is significantly higher in these patients. There is a relationship between urinary endogenous steroid metabolites and lower urinary tract function related to the residual volume in uroflowmetry in postmenopausal women. (PMID: 15808004, 14698830, 12728469). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

16a-Hydroxydehydroisoandrosterone

(1S,2R,5S,10R,11S,13R,15S)-5,13-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-one

C19H28O3 (304.2038338)


16a-Hydroxydehydroisoandrosterone is a metabolite present during pregnancy with increased concentrations as it progresses (PMID 6461703). A reduced level of 16a-Hydroxydehydroisoandrosterone is observed in cases of Placental sulfatase deficiency (PSD), a rare disorder with low estrogen production due to placental enzymatic deficiency. (PMID 2150812) [HMDB] 16a-Hydroxydehydroisoandrosterone is a metabolite present during pregnancy with increased concentrations as it progresses (PMID 6461703). A reduced level of 16a-Hydroxydehydroisoandrosterone is observed in cases of Placental sulfatase deficiency (PSD), a rare disorder with low estrogen production due to placental enzymatic deficiency. (PMID 2150812). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

6beta-Hydroxytestosterone

(1S,2R,8R,10R,11S,14S,15S)-8,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure.

   

w Hydroxy testosterone

(1S,2S,10R,11S,14S,15S)-14-hydroxy-2-(hydroxymethyl)-15-methyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


This compound belongs to the family of Androgens and Derivatives. These are hydroxylated C19 steroid hormones. They are known to favour the development of masculine characteristics. They also show profound effects on scalp and body hair in humans

   
   

16alpha-Hydroxytestosterone

16alpha,17beta-Dihydroxy-4-androsten-3-one

C19H28O3 (304.2038338)


   

NCIOpen2_007952

14alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

15-Hydroxy Testosterone

15alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

1,2,4,5-Tetrahydrotestolactone

1,2,4,5-Tetrahydrotestolactone; D-Homo-17a-oxa-5alpha-androstane-3,17-dione

C19H28O3 (304.2038338)


   

16,17-dihydroxy-16-methylestr-4-en-3-one

16beta,17beta-Dihydroxy-16-methylestr-4-en-3-one

C19H28O3 (304.2038338)


   

NCIOpen2_008609

4beta,5-Epoxy-17beta-hydroxy-5beta-androstan-3-one

C19H28O3 (304.2038338)


   

11beta-Hydroxytestosterone

(2R,14S,15S,17S)-14,17-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

C19H28O3 (304.2038338)


11beta-Hydroxytestosterone is a Testosterone derivative metabolite. Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure. [HMDB] 11beta-Hydroxytestosterone is a Testosterone derivative metabolite. Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure.

   

NSC-37849

3beta-Hydroxy-5alpha-androstane-7,17-dione

C19H28O3 (304.2038338)


   

NCIOpen2_007972

17beta-Hydroxy-5alpha-androstan-3,6-dione

C19H28O3 (304.2038338)


   
   

7a-Hydroxydehydroepiandrosterone

(1S,2R,5S,9S,10R,11S,15S)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-one

C19H28O3 (304.2038338)


7a-Hydroxydehydroepiandrosterone is a major metabolite of dehydroepiandrosterone (DHEA), which is is 7alpha-hydroxylated by the cytochrome P450 7B1 (EC 1.14.13.100, 25-hydroxycholesterol 7alpha-hydroxylase, CYP7B1) in the human brain and liver microsomes. Exposure to the proinflammatory cytokines TNFalpha, IL-1alpha, IL-1beta, and IL-17 increases CYP7B activity in synovial tissue. Increased CYP7B activity leads to higher levels of the DHEA metabolite 7alpha-OH-DHEA in synovial fluid, which may contribute to the maintenance of the chronic inflammation observed in rheumatoid arthritis patients. The glucocorticoid dhydrocorticosterone inhibits the conversion of DHEA to 7a-Hydroxydehydroepiandrosterone. The total levels of 7a-Hydroxydehydroepiandrosterone are increased in serum of patients with Alzheimers disease. (PMID: 17467270, 15751070, 12667489, 9520908) [HMDB] 7a-Hydroxydehydroepiandrosterone is a major metabolite of dehydroepiandrosterone (DHEA), which is is 7alpha-hydroxylated by the cytochrome P450 7B1 (EC 1.14.13.100, 25-hydroxycholesterol 7alpha-hydroxylase, CYP7B1) in the human brain and liver microsomes. Exposure to the proinflammatory cytokines TNFalpha, IL-1alpha, IL-1beta, and IL-17 increases CYP7B activity in synovial tissue. Increased CYP7B activity leads to higher levels of the DHEA metabolite 7alpha-OH-DHEA in synovial fluid, which may contribute to the maintenance of the chronic inflammation observed in rheumatoid arthritis patients. The glucocorticoid dhydrocorticosterone inhibits the conversion of DHEA to 7a-Hydroxydehydroepiandrosterone. The total levels of 7a-Hydroxydehydroepiandrosterone are increased in serum of patients with Alzheimers disease. (PMID: 17467270, 15751070, 12667489, 9520908). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

1alpha-Hydroxytestosterone

1alpha-Hydroxytestosterone

C19H28O3 (304.2038338)


   

12-epi-fischerindole U

12-epi-Fischerindole U; (6aS,9S,10R,10aS)-9-Ethenyl-10-isocyano-6,6,9-trimethyl-5,6,6a,7,8,9,10,10a-octahydroindeno[2,1-b]indole

C21H24N2 (304.1939384)


A tetracyclic indole alkaloid that is produced by the Stigonematales genus of cyanobacteria.

   

hapalindole U

12-epi-Hapalindole H

C21H24N2 (304.1939384)


A hapalindole that is hapalindole H in which the octahydronaphthalene ring junction carbons both have S configuration instead of R.

   

11beta,17beta-Dihydroxy-4-androsten-3-one

(1S,2R,10S,11S,14S,15S,17S)-14,17-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


This compound belongs to the family of Androgens and Derivatives. These are hydroxylated C19 steroid hormones. They are known to favour the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.

   

hapalindole H

hapalindole H

C21H24N2 (304.1939384)


A tetracyclic hapalindole alkaloid that is produced by the Stigonematales genus of cyanobacteria.

   

12-epi-Hapalindole U

12-epi-Hapalindole U

C21H24N2 (304.1939384)


A tetracyclic hapalindole that is hapalindole U in which the carbon bearing the vinyl group has S configuration instead of R. It is produced by the Stigonematales genus of cyanobacteria.

   

3-geranyl-3-[(Z)-2-isocyanoethenyl]-1H-indole

3-geranyl-3-[(Z)-2-isocyanoethenyl]-1H-indole

C21H24N2 (304.1939384)


   

ST 19:2;O3

(3S,7R,8R,9S,10R,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one

C19H28O3 (304.2038338)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones A 17beta-hydroxy steroid that is testosterone bearing an additional hydroxy substituent at the 6beta-position. C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C274 - Antineoplastic Agent > C129818 - Antineoplastic Hormonal/Endocrine Agent > C481 - Antiestrogen C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C1740 - Aromatase Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C147908 - Hormone Therapy Agent > C547 - Hormone Antagonist

   

cis-[8]-Shogaol

4-Dodecen-3-one, 1-(4-hydroxy-3-methoxyphenyl)-, (4E)-

C19H28O3 (304.2038338)


cis-[8]-Shogaol is found in ginger. cis-[8]-Shogaol is isolated from ginger (Zingiber officinale) [DFC] (Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC. [8]-Shogaol is a monomethoxybenzene, an enone and a member of phenols. (8)-Shogaol is a natural product found in Zingiber officinale with data available. See also: Ginger (part of). Constituent of grains of paradise (Amomum melegueta) and (Zingiber officinale) [DFC]. [8]-Shogaol is found in ginger. [8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity (IC50=5 μM) and inhibits COX-2 (IC50=17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells[1][2][3][4]. [8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity (IC50=5 μM) and inhibits COX-2 (IC50=17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells[1][2][3][4].

   

19-Hydroxytestosterone

(2S,10R,14S,15S)-14-hydroxy-2-(hydroxymethyl)-15-methyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


19-Hydroxytestosterone is an intermediate in Androgen and estrogen metabolism. 19-Hydroxytestosterone is the 4th to last step in the synthesis of 16-Glucuronide-estriol. It is generated from Testosterone via the enzyme cytochrome P450 (EC 1.14.14.1) and then converted to 19-Oxotestosterone.

   

10-Acetoxy-8-heptadecene-4,6-diyn-3-ol

(9E)-15-hydroxyheptadec-9-en-11,13-diyn-8-yl acetate

C19H28O3 (304.2038338)


10-Acetoxy-8-heptadecene-4,6-diyn-3-ol is found in tea. 10-Acetoxy-8-heptadecene-4,6-diyn-3-ol is a constituent of Panax ginseng (ginseng). Constituent of Panax ginseng (ginseng). 10-Acetoxy-8-heptadecene-4,6-diyn-3-ol is found in tea.

   

Ginsenoyne G

8-(3-Heptyloxiran-2-yl)octa-4,6-diyn-3-yl acetic acid

C19H28O3 (304.2038338)


Ginsenoyne G is found in tea. Ginsenoyne G is isolated from ginseng root. Isolated from ginseng root. Ginsenoyne G is found in tea.

   

16-Oxoandrostenediol

(2R,5S,14R,15S)-5,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-13-one

C19H28O3 (304.2038338)


16-Oxoandrostenediol is a naturally occurring androgenic steroid hormone generated by the adrenal glands. It has been found in the urine of newborn infants. Secretion of this steroid is suppressed by dexamethasone. Levels of this hormone are almost absent by 5 months of age. ((Steroids (1964), 3(1), 77-83.) ). 16-Oxoandrostenediol is a natural hormone with androgenic activity and that two potent antiandrogens: hydroxyflutamide (Eulexin) and bicalutamide (Casodex). 16-Oxoandrostenediol is a naturally occurring androgenic steroid hormone generated by the adrenal glands. It has been found in the urine of newborn infants. Secretion of this steroid is suppressed by dexamethasone. Levels of this hormone are almost absent by 5 months of age. ((Steroids (1964), 3(1), 77-83.) )

   

3alpha,16beta-Dihydroxyandrostenone

(1S,2R,5R,10R,11S,13S,15S)-5,13-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-one

C19H28O3 (304.2038338)


3alpha,16beta-Dihydroxyandrostenone belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favour the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Thus, 3alpha,16beta-dihydroxyandrostenone is considered to be a steroid lipid molecule. 3alpha,16beta-Dihydroxyandrostenone is an unusual steroid found in the urinary excretion of a subject having a virilizing malignant adrenocortical tumor; apparent 21-steroid hydroxylase deficiency is discussed in the light of these results as well as the hormonogenesis enzymatic induction of the tumour biopsy (PMID: 198067). 3a,16b-Dihydroxyandrostenone is an unusual steroid found in the urinary excretion of a subject having a virilizing malignant adrenocortical tumor; apparent 21-steroid hydroxylase deficiency is discussed at the light of these results and of the hormonogenesis enzymatic induction of the tumour biopsy. (PMID 198067) [HMDB]

   

3alpha,16alpha-Dihydroxyandrostenone

(1S,2R,5R,10R,11S,13R,15S)-5,13-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-one

C19H28O3 (304.2038338)


3alpha,16alpha-Dihydroxyandrostenone belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favour the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Thus, 3alpha,16alpha-dihydroxyandrostenone is considered to be a steroid lipid molecule. 3alpha,16alpha-Dihydroxyandrostenone is the most abundant single urinary metabolite of 16alpha-hydroxydehydroisoandrosterone present in normal, non-pregnant humans (PMID: 6049445). 3alpha,16alpha-Dihydroxyandrostenone was found in the urine sample from a patient who had an inoperable asymptomatic adrenal carcinoma and who excreted about 5 mg/day (PMID: 4733093). 3alpha,16-Dihydroxyandrostenone is a urinary C19 steroid usually present at a very low level in normal pregnancy; however, it is increased in women with androgenic alopecia (PMID: 10751586). 3a,16a-Dihydroxyandrostenone is the most abundant single urinary metabolite of 16a-hydroxydehydroisoandrosterone (PMID 6049445), present in normal, non-pregnant human. It was found in the urine sample from a patient who had an inoperable asymptomatic adrenal carcinoma and who excreted about 5 mg/day (PMID 4733093) [HMDB]

   

7b-Hydroxydehydroepiandrosterone

(3S,7R,8R,9S,10R,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one

C19H28O3 (304.2038338)


7b-Hydroxydehydroepiandrosterone is one of the major metabolites of dehydroepiandrosterone. Dehydroepiandrosterone (DHEA) is a precursor of testosterone. DHEA) is 7a-hydroxylated by the cytochrome P450 7B1 (CYP7B1) in the human brain and liver. This produces 7a-hydroxy-DHEA that is a substrate for 11b-hydroxysteroid dehydrogenase type 1 (11b-HSD1) which exists in the same tissues and carries out the inter-conversion of 7a- and 7b-hydroxy-DHEA through a 7-oxo-intermediary. Both 7a-hydroxy-DHEA and 7b-hydroxy-DHEA competitively inhibited the cortisol oxidation, 7b-hydroxy-DHEA being seven times more potent in humans. Distinct species-specific routes of metabolism of DHEA and the interconversion of its metabolites obviate extrapolation of animal studies to humans. (PMID: 17467270, 12667489) [HMDB] 7b-Hydroxydehydroepiandrosterone is one of the major metabolites of dehydroepiandrosterone. Dehydroepiandrosterone (DHEA) is a precursor of testosterone. DHEA) is 7a-hydroxylated by the cytochrome P450 7B1 (CYP7B1) in the human brain and liver. This produces 7a-hydroxy-DHEA that is a substrate for 11b-hydroxysteroid dehydrogenase type 1 (11b-HSD1) which exists in the same tissues and carries out the inter-conversion of 7a- and 7b-hydroxy-DHEA through a 7-oxo-intermediary. Both 7a-hydroxy-DHEA and 7b-hydroxy-DHEA competitively inhibited the cortisol oxidation, 7b-hydroxy-DHEA being seven times more potent in humans. Distinct species-specific routes of metabolism of DHEA and the interconversion of its metabolites obviate extrapolation of animal studies to humans. (PMID: 17467270, 12667489). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

2beta-Hydroxytestosterone

(2R,4S,14S,15S)-4,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


2beta-Hydroxytestosterone is a Testosterone derivative metabolite. Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure.

   

1-Hydroxytestosterone

1,17-Dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O3 (304.2038338)


   

15-Hydroxytestosterone

15,17-Dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O3 (304.2038338)


   

16beta-Hydroxydehydroepiandrosterone

5,13-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-one

C19H28O3 (304.2038338)


   

4-Androsten-6-beta,17-beta-diol-3-one

8,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


   

4-Hydroxytestosterone

6,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

C19H28O3 (304.2038338)


   

3beta,7-Dihydroxyandrosta-5-ene-17-one

5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-one

C19H28O3 (304.2038338)


   

7alpha,17beta-Dihydroxyandrost-4-en-3-one

9,14-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


   

11,17beta-Dihydroxyandrost-4-en-3-one

14,17-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C19H28O3 (304.2038338)


   

Quinupramine

2-{1-azabicyclo[2.2.2]octan-3-yl}-2-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,11,13-hexaene

C21H24N2 (304.1939384)


N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants > N06AA - Non-selective monoamine reuptake inhibitors C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent > C94727 - Tricyclic Antidepressant

   

(8R,9S,10S,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,3-dione

(8R,9S,10S,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,3-dione

C19H28O3 (304.2038338)


   

ent-15-Nor-14-oxo-8(17),12E-labdadiene-18-oic acid

ent-15-Nor-14-oxo-8(17),12E-labdadiene-18-oic acid

C19H28O3 (304.2038338)


   

Acalycixeniolide L

Acalycixeniolide L

C19H28O3 (304.2038338)


   
   
   

Merilactone

(+)-Merilactone

C19H28O3 (304.2038338)


   

3-Acetoxy-9-heptadecene-4,6-diyn-8-ol.

3-Acetoxy-9-heptadecene-4,6-diyn-8-ol.

C19H28O3 (304.2038338)


   

Quinupramine

Quinupramine

C21H24N2 (304.1939384)


N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants > N06AA - Non-selective monoamine reuptake inhibitors C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent > C94727 - Tricyclic Antidepressant

   
   

15-Nor-14-oxolabda-8(17),12-dien-18-oic acid

15-Nor-14-oxolabda-8(17),12-dien-18-oic acid

C19H28O3 (304.2038338)


   

3beta-Hydroxy-5alpha-androstan-7,16-dion

3beta-Hydroxy-5alpha-androstan-7,16-dion

C19H28O3 (304.2038338)


   
   

16beta-Hydroxy-5alpha-androstan-3,6-dion|16beta-hydroxy-5alpha-androstane-3,6-dione

16beta-Hydroxy-5alpha-androstan-3,6-dion|16beta-hydroxy-5alpha-androstane-3,6-dione

C19H28O3 (304.2038338)


   

ent-7beta-hydroxy-15-oxokaur-16-en-18-ol

ent-7beta-hydroxy-15-oxokaur-16-en-18-ol

C19H28O3 (304.2038338)


   
   
   

2alpha,16-dihydroxykolavenic acid lactone

2alpha,16-dihydroxykolavenic acid lactone

C19H28O3 (304.2038338)


   
   
   

11alpha-Hydroxy-5alpha-androstan-3,16-dion|11alpha-hydroxy-5alpha-androstane-3,16-dion

11alpha-Hydroxy-5alpha-androstan-3,16-dion|11alpha-hydroxy-5alpha-androstane-3,16-dion

C19H28O3 (304.2038338)


   

(13beta,14beta)-13,14-Epoxy-4-hydroxy-19-nor-7-abieten-6-one

(13beta,14beta)-13,14-Epoxy-4-hydroxy-19-nor-7-abieten-6-one

C19H28O3 (304.2038338)


   

caribenol B

caribenol B

C19H28O3 (304.2038338)


A cyclic terpene ketone that is 2a,3,4,5,5a,6,7,8-octahydroacenaphthylen-1(2H)-one substituted by hydroxy groups at positions 2 and 2a, methyl groups at positions 2, 5 and 8 and a 2-methylprop-1-en-1-yl group at position 3. It is isolated from the the West Indian gorgonian octocoral Pseudopterogorgia elisabethae and exhibits antitubercular and antimalarial activity.

   

2,14-dihydroxycalamen-14-O-isobutyrate

2,14-dihydroxycalamen-14-O-isobutyrate

C19H28O3 (304.2038338)


   

7alpha-Hydroxy-5alpha-androstan-2,16-dion

7alpha-Hydroxy-5alpha-androstan-2,16-dion

C19H28O3 (304.2038338)


   
   

Ac-15alpha-15-Hydroxy-17-nor-5,6-seco-7,9(11)-spongiadien-16,15-olide

Ac-15alpha-15-Hydroxy-17-nor-5,6-seco-7,9(11)-spongiadien-16,15-olide

C19H28O3 (304.2038338)


   
   

ent-13-norisocopalen-15-al-18-oic acid

ent-13-norisocopalen-15-al-18-oic acid

C19H28O3 (304.2038338)


   

ent-15,16-Epoxy-3-oxa-kauran-2-one

ent-15,16-Epoxy-3-oxa-kauran-2-one

C19H28O3 (304.2038338)


   

Flavoglaucin

Flavoglaucin

C19H28O3 (304.2038338)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates A natural product found in Eurotium repens.

   

19-norisopimara-4(18),8(14),15-triene-2alpha,7beta,17-triol

19-norisopimara-4(18),8(14),15-triene-2alpha,7beta,17-triol

C19H28O3 (304.2038338)


   
   
   

16alpha,17-dihydroxy-3-oxo-19-nor-ent-kaur-4-ene

16alpha,17-dihydroxy-3-oxo-19-nor-ent-kaur-4-ene

C19H28O3 (304.2038338)


   

4-Oxo-Delta9,Delta11,Delta13,Delta15-octadecatetraen-saeure-methylester

4-Oxo-Delta9,Delta11,Delta13,Delta15-octadecatetraen-saeure-methylester

C19H28O3 (304.2038338)


   

10alpha,19-dihydroxy-15,16-epoxy-8(17),13(16),14-nor-ent-labdatriene|10??,19-Dihydroxy-15,16-epoxy-8(17),13(16),14-nor-ent-labdatriene

10alpha,19-dihydroxy-15,16-epoxy-8(17),13(16),14-nor-ent-labdatriene|10??,19-Dihydroxy-15,16-epoxy-8(17),13(16),14-nor-ent-labdatriene

C19H28O3 (304.2038338)


   
   

16,17-dihydroxy-19-nor-ent-kaur-9(11)-en-3-one

16,17-dihydroxy-19-nor-ent-kaur-9(11)-en-3-one

C19H28O3 (304.2038338)


   

18-nor-abieta-8,11,13-triene-4alpha,7alpha,15-triol

18-nor-abieta-8,11,13-triene-4alpha,7alpha,15-triol

C19H28O3 (304.2038338)


   

15-isobutyryloxycostunolide

15-isobutyryloxycostunolide

C19H28O3 (304.2038338)


   

2-Dodecanone, 12-(1,3-benzodioxol-5-yl)-

2-Dodecanone, 12-(1,3-benzodioxol-5-yl)-

C19H28O3 (304.2038338)


   

dodec-5-enyl 4-hydroxybenzoate

dodec-5-enyl 4-hydroxybenzoate

C19H28O3 (304.2038338)


   

(E)-2-(hept-1-enyl)-3-(hydroxymethyl)-5-(3-methylbut-2-enyl)benzene-1,4-diol|repenol A

(E)-2-(hept-1-enyl)-3-(hydroxymethyl)-5-(3-methylbut-2-enyl)benzene-1,4-diol|repenol A

C19H28O3 (304.2038338)


   

(4E,6R,7R,11S)-6,7-dihydroxy-4,15,15-trimethyl-8-methylidenebicyclo[9.3.1]pentadeca-1(14),4-dien-2-one|cespitulin E

(4E,6R,7R,11S)-6,7-dihydroxy-4,15,15-trimethyl-8-methylidenebicyclo[9.3.1]pentadeca-1(14),4-dien-2-one|cespitulin E

C19H28O3 (304.2038338)


   

(rel-8R)-9-oxo-9,10-seco-labda-5(10),13-dien-15,16-olide|vitextrifolin E

(rel-8R)-9-oxo-9,10-seco-labda-5(10),13-dien-15,16-olide|vitextrifolin E

C19H28O3 (304.2038338)


   

7beta-(Isobutyryloxy)longipinen-1-on

7beta-(Isobutyryloxy)longipinen-1-on

C19H28O3 (304.2038338)


   

4-Epimer,4-hydroperoxide,7alpha-alcohol-4-Hydroxy-18-nor-8,11,13-abietatrien-7-one|7alpha-hydroxy-19-norabieta-8,11,13-triene-4-hydroperoxide

4-Epimer,4-hydroperoxide,7alpha-alcohol-4-Hydroxy-18-nor-8,11,13-abietatrien-7-one|7alpha-hydroxy-19-norabieta-8,11,13-triene-4-hydroperoxide

C19H28O3 (304.2038338)


   

(+/-)-8-{4-oxo-5-[E-pent-2-en-E-ylidene]cyclopent-2-enyl}octanoic acid methyl ester|methyl 8-<(2E)-3-oxo-2-((E)-2-pentenylidene)-4-cyclopentenyl>octanoate

(+/-)-8-{4-oxo-5-[E-pent-2-en-E-ylidene]cyclopent-2-enyl}octanoic acid methyl ester|methyl 8-<(2E)-3-oxo-2-((E)-2-pentenylidene)-4-cyclopentenyl>octanoate

C19H28O3 (304.2038338)


   

ent-15-nor-14-oxo-3,4-seco-4,8,12(E)-labdatrien-3-oic acid

ent-15-nor-14-oxo-3,4-seco-4,8,12(E)-labdatrien-3-oic acid

C19H28O3 (304.2038338)


   

19-nor-8,14beta-dihydroxy-15-isopimaren-7-one

19-nor-8,14beta-dihydroxy-15-isopimaren-7-one

C19H28O3 (304.2038338)


   

13-isobutyryloxy-3-oxo-silphinene

13-isobutyryloxy-3-oxo-silphinene

C19H28O3 (304.2038338)


   

methyl ent-2,4-seco-4-oxo-3,19-dinorbeyer-15-en-2-oate

methyl ent-2,4-seco-4-oxo-3,19-dinorbeyer-15-en-2-oate

C19H28O3 (304.2038338)


   
   
   

1-Ac-(E)-8-Heptadecene-4,6-diyne-1,10-diol|17-acetoxy-heptadec-9t-ene-11,13-diyn-8-ol|Heptadecen-(8t)-diin-(4,6)-diol-(1,10)-monoacetat-(1)|trans-1-Acetoxy-heptadecen-(8)-diin-(4.6)-ol-(10)

1-Ac-(E)-8-Heptadecene-4,6-diyne-1,10-diol|17-acetoxy-heptadec-9t-ene-11,13-diyn-8-ol|Heptadecen-(8t)-diin-(4,6)-diol-(1,10)-monoacetat-(1)|trans-1-Acetoxy-heptadecen-(8)-diin-(4.6)-ol-(10)

C19H28O3 (304.2038338)


   
   

7-Hydroxy-kaurenolid

7-Hydroxy-kaurenolid

C19H28O3 (304.2038338)


   

(-)-methyl 13-oxo-15,16-dinorlabda-8(17),11E-dien-19-oate|14,15-bisnor-13-oxo-8(17),11(E)-labdadien-19-oic acid methyl ester|15,16-dinorlabda-8(20),11E-dien-13-one-19-oic acid methyl ester|methyl 13-oxo-14,15-dinorlabda-8(17),11E-dien-19-oate

(-)-methyl 13-oxo-15,16-dinorlabda-8(17),11E-dien-19-oate|14,15-bisnor-13-oxo-8(17),11(E)-labdadien-19-oic acid methyl ester|15,16-dinorlabda-8(20),11E-dien-13-one-19-oic acid methyl ester|methyl 13-oxo-14,15-dinorlabda-8(17),11E-dien-19-oate

C19H28O3 (304.2038338)


   

6beta,16beta-Dihydroxyandrost-4-en-3-on

6beta,16beta-Dihydroxyandrost-4-en-3-on

C19H28O3 (304.2038338)


   

11alpha,16beta-Dihydroxyandrost-4-en-3-on

11alpha,16beta-Dihydroxyandrost-4-en-3-on

C19H28O3 (304.2038338)


   

Methyl-lambertianat

Methyl-lambertianat

C19H28O3 (304.2038338)


   
   

Trisporat A-methylester

Trisporat A-methylester

C19H28O3 (304.2038338)


   
   

12-epi-hapalindole C isonitrile

12-epi-hapalindole C isonitrile

C21H24N2 (304.1939384)


   

2-heptyl-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde

NCGC00381406-01!2-heptyl-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde

C19H28O3 (304.2038338)


   

(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one

NCGC00169651-02!(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one

C19H28O3 (304.2038338)


   

C19H28O3_5,9-Dimethyl-14-oxotetracyclo[11.2.1.0~1,10~.0~4,9~]hexadecane-5-carboxylic acid

NCGC00347546-02_C19H28O3_5,9-Dimethyl-14-oxotetracyclo[11.2.1.0~1,10~.0~4,9~]hexadecane-5-carboxylic acid

C19H28O3 (304.2038338)


   

(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one [IIN-based on: CCMSLIB00000849054]

NCGC00169651-02!(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one [IIN-based on: CCMSLIB00000849054]

C19H28O3 (304.2038338)


   

(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one [IIN-based: Match]

NCGC00169651-02!(E)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one [IIN-based: Match]

C19H28O3 (304.2038338)


   

h_150_7a_hydroxy_dhea

h_150_7a_hydroxy_dhea

C19H28O3 (304.2038338)


   

h_118_4_hydroxytestosterone

h_118_4_hydroxytestosterone

C19H28O3 (304.2038338)


   

h_266_Oxandrolone_m3

h_266_Oxandrolone_m3

C19H28O3 (304.2038338)


   

16-Oxoandrostenediol

16-Oxoandrostenediol

C19H28O3 (304.2038338)


   

3a,16a-Dihydroxyandrostenone

3a,16a-Dihydroxyandrostenone

C19H28O3 (304.2038338)


   

3a,16b-Dihydroxyandrostenone

3a,16b-Dihydroxyandrostenone

C19H28O3 (304.2038338)


   

3a,16-Dihydroxyandrostenone

3a,16-Dihydroxyandrostenone

C19H28O3 (304.2038338)


   

4-Hydroxytestosterone

4-Hydroxy Testosterone

C19H28O3 (304.2038338)


C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C274 - Antineoplastic Agent > C129818 - Antineoplastic Hormonal/Endocrine Agent > C481 - Antiestrogen C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C1740 - Aromatase Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C147908 - Hormone Therapy Agent > C547 - Hormone Antagonist

   

7b-Hydroxydehydroepiandrosterone

7b-Hydroxydehydroepiandrosterone

C19H28O3 (304.2038338)


   

CIS-8-SHOGAOL

(4e)-1-(4-hydroxy-3-methoxyphenyl)dodec-4-en-3-one

C19H28O3 (304.2038338)


   

Ginsenoyne G

8-(3-heptyloxiran-2-yl)octa-4,6-diyn-3-yl acetate

C19H28O3 (304.2038338)


   

10-Acetoxy-8-heptadecene-4,6-diyn-3-ol

(9E)-15-hydroxyheptadec-9-en-11,13-diyn-8-yl acetate

C19H28O3 (304.2038338)


   

(5S,8R,9S,10S)-18-nor-cleroda-13-en-16,15-olide-3-one

(5S,8R,9S,10S)-18-nor-cleroda-13-en-16,15-olide-3-one

C19H28O3 (304.2038338)


   

(5S,8R,9S,10S)-18-nor-cleroda-13-en-16,15-olide-4-one

(5S,8R,9S,10S)-18-nor-cleroda-13-en-16,15-olide-4-one

C19H28O3 (304.2038338)


   

2-(2,2,2-Trimethylacetamido) pyridine-3-boronic acid pinacol ester

2-(2,2,2-Trimethylacetamido) pyridine-3-boronic acid pinacol ester

C16H25BN2O3 (304.19581300000004)


   

(4-methoxyphenyl) 4-pentylcyclohexane-1-carboxylate

(4-methoxyphenyl) 4-pentylcyclohexane-1-carboxylate

C19H28O3 (304.2038338)


   

5-Methoxy-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

5-Methoxy-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

C17H28N2OSi (304.1970798)


   

(4-ethoxyphenyl) 4-butylcyclohexane-1-carboxylate

(4-ethoxyphenyl) 4-butylcyclohexane-1-carboxylate

C19H28O3 (304.2038338)


   

5-(Morpholinomethyl)pyridine-3-boronic acid pinacol ester

5-(Morpholinomethyl)pyridine-3-boronic acid pinacol ester

C16H25BN2O3 (304.19581300000004)


   

6-pivalamidopyridine-3-boronic acid pinacol ester

6-pivalamidopyridine-3-boronic acid pinacol ester

C16H25BN2O3 (304.19581300000004)


   

N,N-Diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-Pyridinecarboxamide

N,N-Diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-Pyridinecarboxamide

C16H25BN2O3 (304.19581300000004)


   

4-Methoxy-1-(triisopropylsilyl)-1H-pyrrolo[2,3-c]pyridine

4-Methoxy-1-(triisopropylsilyl)-1H-pyrrolo[2,3-c]pyridine

C17H28N2OSi (304.1970798)


   

4-((5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDIN-2-YL)METHYL)MORPHOLINE

4-((5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDIN-2-YL)METHYL)MORPHOLINE

C16H25BN2O3 (304.19581300000004)


   

trans,trans-4-(3,4-Difluorophenyl)-4-vinylbicyclohexyl

trans,trans-4-(3,4-Difluorophenyl)-4-vinylbicyclohexyl

C20H26F2 (304.200246)


   

19-Hydroxy Androstendione-19-d2

19-Hydroxy Androstendione-19-d2

C19H24D2O3 (304.200738956)


   

4-METHOXY-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

4-METHOXY-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

C17H28N2OSi (304.1970798)


   

6alpha-Hydroxytestosterone

(6S,8R,9S,10R,13S,14S,17S)-6,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O3 (304.2038338)


   

4-Ethoxyphenyl 4-butylcyclohexanecarboxylate

4-Ethoxyphenyl 4-butylcyclohexanecarboxylate

C19H28O3 (304.2038338)


   

N,N-DIETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE

N,N-DIETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE

C16H25BN2O3 (304.19581300000004)


   
   

1,3-DIMESITYL-1H-IMIDAZOL-3-IUM-2-IDE

1,3-DIMESITYL-1H-IMIDAZOL-3-IUM-2-IDE

C21H24N2 (304.1939384)


   

2-(4-Methylpiperazin-1-yl)pyrimidine-5-boronic acid pinacol ester

2-(4-Methylpiperazin-1-yl)pyrimidine-5-boronic acid pinacol ester

C15H25BN4O2 (304.207046)


   

2-(dimethylamino)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide

2-(dimethylamino)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide

C16H25BN2O3 (304.19581300000004)


   

4-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

4-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

C19H28O3 (304.2038338)


   

2α-Hydroxy Testosterone

2alpha-Hydroxytestosterone

C19H28O3 (304.2038338)


An androstanoid that is testosterone substituted by a alpha-hydroxy group at position 2. A natural product found in Daphnia magna exposed to the biocide tributyltin.

   

5-Methyl-6-(morpholin-4-yl)pyridine-3-boronic acid pinacol ester

5-Methyl-6-(morpholin-4-yl)pyridine-3-boronic acid pinacol ester

C16H25BN2O3 (304.19581300000004)


   

1-Propyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

1-Propyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

C16H25BN2O3 (304.19581300000004)


   

1-propan-2-yl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

1-propan-2-yl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

C16H25BN2O3 (304.19581300000004)


   

4-Hydroxy-19-normethyltestosterone

4-Hydroxy-19-normethyltestosterone

C19H28O3 (304.2038338)


   

16beta-Hydroxytestosterone

16beta-Hydroxytestosterone

C19H28O3 (304.2038338)


An androstanoid that is testosterone substituted by a beta-hydroxy group at position 16. A natural product found in Daphnia magna exposed to the biocide tributyltin.

   
   

11alpha-Hydroxytestosterone

11alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

3beta-Hydroxy-5alpha-androstane-7,17-dione

3beta-Hydroxy-5alpha-androstane-7,17-dione

C19H28O3 (304.2038338)


   

6-Ketodihydrotestosterone

17beta-Hydroxy-5alpha-androstan-3,6-dione

C19H28O3 (304.2038338)


   

4beta,5-Epoxy-17beta-hydroxy-5beta-androstan-3-one

4beta,5-Epoxy-17beta-hydroxy-5beta-androstan-3-one

C19H28O3 (304.2038338)


   

6-Methyl-9-(2-(2-methyl-5-pyridyl)ethyl)-1,2,3,4-tetrahydrocarbazole

6-Methyl-9-(2-(2-methyl-5-pyridyl)ethyl)-1,2,3,4-tetrahydrocarbazole

C21H24N2 (304.1939384)


   

8-Shogaol

1-(3,4-Dimethoxyphenyl)-4-decen-3-one

C19H28O3 (304.2038338)


Constituent of ginger (Zingiber officinale) [DFC]. 1-(3,4-Dimethoxyphenyl)-4-decen-3-one is found in ginger. [8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity (IC50=5 μM) and inhibits COX-2 (IC50=17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells[1][2][3][4]. [8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity (IC50=5 μM) and inhibits COX-2 (IC50=17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells[1][2][3][4].

   

6 β hydroxy testosterone

6beta-hydroxytestosterone

C19H28O3 (304.2038338)


Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure. [HMDB]

   

19-Hydroxytestosterone

Androst-4-en-3-one,17,19-dihydroxy-, (17b)-

C19H28O3 (304.2038338)


A 3-oxo Delta(4)-steroid that is testosterone which is substituted by a hydroxy group at positions 19. 19-Hydroxytestosterone is an intermediate in Androgen and estrogen metabolism. 19-Hydroxytestosterone is the 4th to last step in the synthesis of 16-Glucuronide-estriol. It is generated from Testosterone via the enzyme cytochrome P450 (EC 1.14.14.1) and then converted to 19-Oxotestosterone. [HMDB]. 19-Hydroxytestosterone is found in many foods, some of which are hedge mustard, tinda, black walnut, and babassu palm.

   

2β-Hydroxy Testosterone

2beta-Hydroxytestosterone

C19H28O3 (304.2038338)


An androstanoid that is testosterone carrying an additional hydroxy substituent at the 2beta-position. 2beta-Hydroxytestosterone is a Testosterone derivative metabolite. Testosterone is reported to have an acute vasodilating action in vitro, an effect that may impart a favourable haemodynamic response in patients with chronic heart failure. [HMDB]

   

14 alpha-Hydroxytestosterone

14 alpha-Hydroxytestosterone

C19H28O3 (304.2038338)


   

5,9-Dimethyl-14-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

5,9-Dimethyl-14-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

C19H28O3 (304.2038338)


   

12-Epi-hapalindole J isonitrile

12-Epi-hapalindole J isonitrile

C21H24N2 (304.1939384)


   

12-epi-Hapalindole C

12-epi-Hapalindole C

C21H24N2 (304.1939384)


   

Monacolin L

Monacolin L

C19H28O3 (304.2038338)


A polyketide that is 1-ethyl-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalene in which one of the methyl hydrogens from the ethyl group is replaced by a 4-hydroxy-6-ketopyran-2-yl group.

   

(6aR,9S,10R,10aR)-10-isocyano-6,6,9-trimethyl-9-vinyl-2,6,6a,7,8,9,10,10a-octahydronaphtho[1,2,3-cd]indole

(6aR,9S,10R,10aR)-10-isocyano-6,6,9-trimethyl-9-vinyl-2,6,6a,7,8,9,10,10a-octahydronaphtho[1,2,3-cd]indole

C21H24N2 (304.1939384)


   

15alpha-Hydroxytestosterone

15alpha-Hydroxytestosterone

C19H28O3 (304.2038338)


   

1-Hydroxyandrostan-3,17-dione

1-Hydroxyandrostan-3,17-dione

C19H28O3 (304.2038338)


   

2-geranyl-3-[(Z)-2-isocyanoethenyl]-3H-indole

2-geranyl-3-[(Z)-2-isocyanoethenyl]-3H-indole

C21H24N2 (304.1939384)


   

2beta,17beta-Dihydroxyandrost-4-en-3-one

2beta,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

(8R,10S,13S,17S)-17-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

(8R,10S,13S,17S)-17-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O3 (304.2038338)


   

(8R,9S,10S,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,3-dione

(8R,9S,10S,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,3-dione

C19H28O3 (304.2038338)


   

[3-Carboxy-2-(3-hydroxyoctanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(3-hydroxyoctanoyloxy)propyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(5-hydroxyoctanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(5-hydroxyoctanoyloxy)propyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(7-hydroxyoctanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(7-hydroxyoctanoyloxy)propyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(6-hydroxyoctanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(6-hydroxyoctanoyloxy)propyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(4-hydroxyoctanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(4-hydroxyoctanoyloxy)propyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(5-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

[3-Carboxy-2-(5-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(3-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

[3-Carboxy-2-(3-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

[3-Carboxy-2-(4-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

[3-Carboxy-2-(4-hydroxy-2-propylpentanoyl)oxypropyl]-trimethylazanium

C15H30NO5+ (304.212387)


   

15-Hydroxytestosterone

15alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


An androstanoid that is testosterone substituted by a alpha-hydroxy group at position 15. A natural product found in Daphnia magna exposed to the biocide tributyltin.

   

14alpha,17beta-Dihydroxyandrost-4-en-3-one

14alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

(e)-2-(Hept-1-enyl)-3-(hydroxymethyl)-5-(3-methylbut-2-enyl)benzene-1,4-diol

(e)-2-(Hept-1-enyl)-3-(hydroxymethyl)-5-(3-methylbut-2-enyl)benzene-1,4-diol

C19H28O3 (304.2038338)


A natural product found in Eurotium repens.

   

2-Hydroxytestosterone

2-Hydroxytestosterone

C19H28O3 (304.2038338)


   

15-norlabda-8(20),12E-diene-14-carboxaldehyde-19-oic acid

15-norlabda-8(20),12E-diene-14-carboxaldehyde-19-oic acid

C19H28O3 (304.2038338)


A natural product found in Metasequoia glyptostroboides.

   

1-Hydroxy-5alpha-androstan-3,17-dione

1-Hydroxy-5alpha-androstan-3,17-dione

C19H28O3 (304.2038338)


   

12-epi-hapalindole C isoniltrile

12-epi-hapalindole C isoniltrile

C21H24N2 (304.1939384)


   

17beta-Hydroxy-3-oxo-5alpha-androstan-19-al

17beta-Hydroxy-3-oxo-5alpha-androstan-19-al

C19H28O3 (304.2038338)


   

16-alpha-Methyl-16-beta-hydroxy-19-nortestosterone

16-alpha-Methyl-16-beta-hydroxy-19-nortestosterone

C19H28O3 (304.2038338)


   
   

4-Ethenyl-3-isocyano-4,8,8-trimethyl-14-azatetracyclo[7.6.1.02,7.013,16]hexadeca-1(15),9(16),10,12-tetraene

4-Ethenyl-3-isocyano-4,8,8-trimethyl-14-azatetracyclo[7.6.1.02,7.013,16]hexadeca-1(15),9(16),10,12-tetraene

C21H24N2 (304.1939384)


   

16a-Hydroxydehydroisoandrosterone

16a-Hydroxydehydroisoandrosterone

C19H28O3 (304.2038338)


   
   

N-methyl-L-valyl-L-tryptophanol(1+)

N-methyl-L-valyl-L-tryptophanol(1+)

C17H26N3O2+ (304.2024916)


   

3-(3-ethenyl-2-isocyano-3-methyl-6-prop-1-en-2-ylcyclohexyl)-1H-indole

3-(3-ethenyl-2-isocyano-3-methyl-6-prop-1-en-2-ylcyclohexyl)-1H-indole

C21H24N2 (304.1939384)


   

Androstdiene-3-hydroxy-17-one

Androstdiene-3-hydroxy-17-one

C19H28O3 (304.2038338)


   

Methyl (3R,6S)-3-(tert-butyldimethylsiloxy)-7-hydroxy-6-methylheptanoate

Methyl (3R,6S)-3-(tert-butyldimethylsiloxy)-7-hydroxy-6-methylheptanoate

C15H32O4Si (304.2069752)


   

16alpha-Hydroxydehydroepiandrosterone

16alpha-Hydroxydehydroepiandrosterone

C19H28O3 (304.2038338)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

11beta-Hydroxytestosterone

Androst-4-en-3-one,11,17-dihydroxy-, (11b,17b)-

C19H28O3 (304.2038338)


An androstanoid that is testosterone carrying an additional hydroxy substituent at the 11beta-position.

   

7alpha-Hydroxydehydroepiandrosterone

7-alpha-Hydroxydehydroepiandrosterone

C19H28O3 (304.2038338)


An androstanoid that is dehydroepiandrosterone carrying an additional hydroxy substituent at the 7alpha-position. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

7alpha-Hydroxytestosterone

7alpha-Hydroxytestosterone

C19H28O3 (304.2038338)


   

(1-Benzyl-1H-quinolin-4-ylidene)-pentyl-amine

(1-Benzyl-1H-quinolin-4-ylidene)-pentyl-amine

C21H24N2 (304.1939384)


   

17-hydroxy-androstan-1,3-dione

17-hydroxy-androstan-1,3-dione

C19H28O3 (304.2038338)


   

11-Oxo etiocholanolone

3alpha-hydroxy-5beta-androstane-11,17-dione

C19H28O3 (304.2038338)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

7a-Hydroxytestosterone

7a-Hydroxytestosterone

C19H28O3 (304.2038338)


   

7beta-Hydroxydehydroepiandrosterone

7beta-Hydroxydehydroepiandrosterone

C19H28O3 (304.2038338)


An androstanoid that is dehydroepiandrosterone carrying an additional hydroxy substituent at the 7beta-position. It is a metabolite of dehydroepiandrosterone.

   

14-Hydroxytestosterone

14alpha,17beta-Dihydroxyandrost-4-en-3-one

C19H28O3 (304.2038338)


   

4beta,5beta-Epoxytestosterone

4beta,5-Epoxy-17beta-hydroxy-5beta-androstan-3-one

C19H28O3 (304.2038338)


   

1beta-hydroxytestosterone

1beta-hydroxytestosterone

C19H28O3 (304.2038338)


   

3beta,6alpha-dihydroxy-5alpha-androst-9(11)-en-17-one

3beta,6alpha-dihydroxy-5alpha-androst-9(11)-en-17-one

C19H28O3 (304.2038338)


   

3-geranyl-3-[(Z)-2-isocyanovinyl]-3H-indole

3-geranyl-3-[(Z)-2-isocyanovinyl]-3H-indole

C21H24N2 (304.1939384)


A member of the class of indoles in which the hydrogens at position 3 of 3H-indole have been replaced by 2-isocyanovinyl and geranyl groups.

   

19-oxo-5alpha-dihydrotestosterone

19-oxo-5alpha-dihydrotestosterone

C19H28O3 (304.2038338)


An androstanoid that is 5alpha-dihydrotestosterone carrying an additional oxo susbstituent at position 19.

   

7alpha -hydroxytestosterone

7alpha -hydroxytestosterone

C19H28O3 (304.2038338)


An androstanoid that is testosterone substituted by a alpha-hydroxy group at position 7. A natural product found in Daphnia magna exposed to the biocide tributyltin

   

Hydroxynonadecapentaenoic acid

Hydroxynonadecapentaenoic acid

C19H28O3 (304.2038338)


   

Hydroxydehydroepiandrosterone

Hydroxydehydroepiandrosterone

C19H28O3 (304.2038338)


   

Hydroxytestosterone

Hydroxytestosterone

C19H28O3 (304.2038338)


   

Ketoetiocholanolone

Ketoetiocholanolone

C19H28O3 (304.2038338)