Exact Mass: 374.2821

Exact Mass Matches: 374.2821

Found 148 metabolites which its exact mass value is equals to given mass value 374.2821, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Dehydrolithocholic acid

3-Oxo-5α-cholan-24-oic Acid

C24H38O3 (374.2821)


D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts D005765 - Gastrointestinal Agents > D002793 - Cholic Acids

   

3,21-dihydroxy-4,4,14-trimethylpregn-8-en-20-one

3beta,21-Dihydroxy-4,4,14-trimethyl-5alpha-pregn-8-en-20-one

C24H38O3 (374.2821)


   

Androst-5-ene-3beta,17beta-diol 3-tetrahydropyranyl ether

3beta-[(Tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17beta-ol

C24H38O3 (374.2821)


   

2-(10-Heptadecenyl)-6-hydroxybenzoic acid

Ginkgolic acid C17:1, primary pharmaceutical reference standard

C24H38O3 (374.2821)


2-(10-Heptadecenyl)-6-hydroxybenzoic acid is found in fats and oils. 2-(10-Heptadecenyl)-6-hydroxybenzoic acid is isolated from Ginkgo biloba (ginkgo). 2-(10-Heptadecenyl)-6-hydroxybenzoic acid is a natural product found in Knema laurina, Ginkgo biloba, and Spondias mombin with data available. Isolated from Ginkgo biloba (ginkgo). 2-(10-Heptadecenyl)-6-hydroxybenzoic acid is found in fats and oils. Ginkgolic acid C17:1, extracted from Ginkgo biloba Leaves, suppresses constitutive and inducible STAT3 activation through induction of PTEN and SHP-1 tyrosine phosphatase. Ginkgolic acid C17:1 has anticancer effects[1]. Ginkgolic acid C17:1, extracted from Ginkgo biloba Leaves, suppresses constitutive and inducible STAT3 activation through induction of PTEN and SHP-1 tyrosine phosphatase. Ginkgolic acid C17:1 has anticancer effects[1].

   

D8'-Merulinic acid C

2-[(8E)-heptadec-8-en-1-yl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


D8-Merulinic acid C is isolated from pistachio shells. Isolated from pistachio shells

   

3b-Hydroxy-5-cholenoic acid

(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

C24H38O3 (374.2821)


3b-Hydroxy-5-cholenoic acid, also known as 3b-hydroxy-chol-5-en-24-oate or cholenate, belongs to the class of organic compounds known as monohydroxy bile acids. These are bile acids bearing a hydroxyl group. Bile acids facilitate fat absorption and cholesterol excretion. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, and depends only on the presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine, and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH, and consequently require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues (PMID: 11316487 , 16037564 , 12576301 , 11907135 ). When present in sufficiently high levels, bile acids can act as hepatotoxins and metabotoxisn. A hepatotoxin causes damage to the liver or liver cells. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Among the primary bile acids, cholic acid is considered to be the least hepatotoxic while deoxycholic acid is the most hepatoxic (PMID: 1641875 ). The liver toxicity of bile acids appears to be due to their ability to peroxidate lipids and to lyse liver cells. Chronically high levels of cholic acid are associated with familial hypercholanemia. In hypercholanemia, bile acids are elevated in the blood. This disease causes liver damage, extensive itching, poor fat absorption, and can lead to rickets due to lack of calcium in bones. The deficiency of normal bile acids in the intestines results in a deficiency of vitamin K, which also adversely affects clotting of the blood. 3b-Hydroxy-5-cholenoic acid is a monohydroxy bile acid of endogenous origin. It is found in biologic fluids beginning in fetal life. (PMID 5567561; 4803245; 93138) Large amounts of 3 beta-hydroxy-5-cholenoic acid could be found in children with the syndrome of hepatic ductular hypoplasia (PMID 3987031) [HMDB] D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts D005765 - Gastrointestinal Agents > D002793 - Cholic Acids 3b-Hydroxy-5-cholenoic acid is a monohydroxy bile acid of endogenous origin and could be found in children with the syndrome of hepatic ductular hypoplasia.

   

3-Oxo-5beta-cholanoic acid

4-{2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl}pentanoic acid

C24H38O3 (374.2821)


   
   
   

2-Thio-acetyl MAGE

S-[2-(hexadecyloxy)-1-(hydroxymethyl)ethyl]ester, ethanethioic acid

C21H42O3S (374.2855)


   

Lithocholenic acid

Lithocholenic acid

C24H38O3 (374.2821)


CONFIDENCE standard compound; INTERNAL_ID 75

   

SCHEMBL8912792

SCHEMBL8912792

C24H38O3 (374.2821)


   

Litophynin A

Litophynin A

C24H38O3 (374.2821)


   

Yuccagenone

Yuccagenone

C24H38O3 (374.2821)


   

2-methoxy-6-(8-pentadecenyl)-benzoic acid methyl ester

2-methoxy-6-(8-pentadecenyl)-benzoic acid methyl ester

C24H38O3 (374.2821)


   

Raspailol A

Raspailol A

C24H38O3 (374.2821)


   

16alpha-ethoxy-18-hydroxy-ent-kaur-11-ene acetate

16alpha-ethoxy-18-hydroxy-ent-kaur-11-ene acetate

C24H38O3 (374.2821)


   

(3beta,5alpha,6beta,14alpha)-3,6-Dihydroxy-4,4,14-trimethylpregn-8-en-20-one

(3beta,5alpha,6beta,14alpha)-3,6-Dihydroxy-4,4,14-trimethylpregn-8-en-20-one

C24H38O3 (374.2821)


   
   

2H-Pyran-2-acetic acid, tetrahydro-6-(10-phenyldecyl)-, methyl ester

2H-Pyran-2-acetic acid, tetrahydro-6-(10-phenyldecyl)-, methyl ester

C24H38O3 (374.2821)


   

2-[(11Z)-heptadec-11-enyl]-6-hydroxybenzoic acid

2-[(11Z)-heptadec-11-enyl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

cananginone D

cananginone D

C24H38O3 (374.2821)


   
   

6-(12-heptadecenyl)salicylic acid

6-(12-heptadecenyl)salicylic acid

C24H38O3 (374.2821)


   

DTXSID10839686

DTXSID10839686

C24H38O3 (374.2821)


   

(Z)-1-(3,4-dihydroxyphenyl)octadec-13-en-5-one|3-Hydroxy,3,14-Didehydro(Z)-1-(4-Hydroxyphenyl)-5-octadecanone

(Z)-1-(3,4-dihydroxyphenyl)octadec-13-en-5-one|3-Hydroxy,3,14-Didehydro(Z)-1-(4-Hydroxyphenyl)-5-octadecanone

C24H38O3 (374.2821)


   

6alpha-butyryloxy-9alpha,13-epoxy-labda-7,14-diene

6alpha-butyryloxy-9alpha,13-epoxy-labda-7,14-diene

C24H38O3 (374.2821)


   

2-(Z,Z)-octadeca-9,12-dienoylcyclohexane-1,3-dione|2-[(9Z,12Z)-octadeca-9,12-dienoyl]cyclohexane-1,3-dione

2-(Z,Z)-octadeca-9,12-dienoylcyclohexane-1,3-dione|2-[(9Z,12Z)-octadeca-9,12-dienoyl]cyclohexane-1,3-dione

C24H38O3 (374.2821)


   

12-O-deacetylnorscalaral B

12-O-deacetylnorscalaral B

C24H38O3 (374.2821)


   

(5alpha,12beta,17beta)-17-acetyl-12-hydroxy-4,4,8,10,14-pentamethylgonan-3-one|cylindrictone E

(5alpha,12beta,17beta)-17-acetyl-12-hydroxy-4,4,8,10,14-pentamethylgonan-3-one|cylindrictone E

C24H38O3 (374.2821)


   

(+)-(10R,7Z,11E,13Z,16Z,19Z)-ethyl 10-hydroxy-7,11,13,16,19-docosapentaenoate

(+)-(10R,7Z,11E,13Z,16Z,19Z)-ethyl 10-hydroxy-7,11,13,16,19-docosapentaenoate

C24H38O3 (374.2821)


   

Pallasone

2,5-CYCLOHEXADIENE-1,4-DIONE, 2-(10Z)-10-HEPTADECEN-1-YL-6-METHOXY-

C24H38O3 (374.2821)


Irisquinone is a natural product found in Iris pallasii, Iris sibirica, and other organisms with data available.

   

3b-Hydroxy-5-cholenoic acid

3b-Hydroxy-5-cholenoic acid

C24H38O3 (374.2821)


D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts D005765 - Gastrointestinal Agents > D002793 - Cholic Acids 3b-Hydroxy-5-cholenoic acid is a monohydroxy bile acid of endogenous origin and could be found in children with the syndrome of hepatic ductular hypoplasia.

   

LITHOCHOL-11-ENIC ACID

LITHOCHOL-11-ENIC ACID

C24H38O3 (374.2821)


   

3-Ketocholanic acid

3-Ketocholanic acid

C24H38O3 (374.2821)


CONFIDENCE standard compound; INTERNAL_ID 76

   

3-Oxo-5b-cholan-24-oic Acid

3-Oxo-5b-cholan-24-oic Acid

C24H38O3 (374.2821)


BA-111-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-111-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

6-Oxo-5b-cholan-24-oic Acid

6-Oxo-5b-cholan-24-oic Acid

C24H38O3 (374.2821)


BA-112-150. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-112-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-112-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-112-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-112-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

7-Oxo-5b-cholanic acid

7-Oxo-5b-cholanic acid

C24H38O3 (374.2821)


BA-113-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-113-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-113-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-113-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

12-Oxo-5b-cholan-24-ic acid

12-Oxo-5b-cholan-24-ic acid

C24H38O3 (374.2821)


BA-114-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-114-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-114-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-114-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

3-Oxo-5a-cholan-24-oic acid

3-Oxo-5a-cholan-24-oic acid

C24H38O3 (374.2821)


BA-120-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-120-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-120-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-120-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

6-Oxo-5a-cholan-24-oic acid

6-Oxo-5a-cholan-24-oic acid

C24H38O3 (374.2821)


BA-121-150. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-121-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-121-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-121-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

7-Oxo-5a-cholan-24-oic acid

7-Oxo-5a-cholan-24-oic acid

C24H38O3 (374.2821)


BA-122-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-122-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-122-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

12-Oxo-5a-cholan-24-oic acid

12-Oxo-5a-cholan-24-oic acid

C24H38O3 (374.2821)


BA-123-120. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-123-90. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-123-60. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan. BA-123-30. In-source decay; 1 microL of the bile acid in MeOH solution was flow injected. Sampling interval was 1 Hz.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 17HP8021 (2017) to the MassBank database committee of the Mass Spectrometry Society of Japan.

   

3-oxo lithocholic acid

3-oxo lithocholic acid

C24H38O3 (374.2821)


   

LITHOCHOL-11-ENIC ACID_major

LITHOCHOL-11-ENIC ACID_major

C24H38O3 (374.2821)


   

(R)-4-((5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

"(R)-4-((5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid"

C24H38O3 (374.2821)


   

(5Z,7E)-(1S,3R)-9,10-seco-5,7,10(19)-cholatriene-1,3,24-triol

1α,24-dihydroxy-25,26,27-trinorvitamin D3 / 1α,24-dihydroxy-25,26,27-trinorcholecalciferol

C24H38O3 (374.2821)


   

3-Oxo-5β-cholan-24-oic Acid

3-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

6-Oxo-5β-cholan-24-oic Acid

6-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

6-Oxo-5α-cholan-24-oic Acid

6-Oxo-5α-cholan-24-oic Acid

C24H38O3 (374.2821)


   

7-Oxo-5β-cholan-24-oic Acid

7-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

12-Oxo-5β-cholan-24-oic Acid

12-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

12-Oxo-5α-cholan-24-oic Acid

12-Oxo-5α-cholan-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxychol-4-en-24-oic Acid

3α-Hydroxychol-4-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxychol-4-en-24-oic Acid

3β-Hydroxychol-4-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxychol-5-en-24-oic Acid

3α-Hydroxychol-5-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxy-chol-5-en-24-oic Acid

3β-Hydroxy-chol-5-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-6-en-24-oic Acid

3α-Hydroxy-5β-chol-6-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxy-5β-chol-6-en-24-oic Acid

3β-Hydroxy-5β-chol-6-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-7-en-24-oic Acid

3α-Hydroxy-5β-chol-7-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxy-5α-chol-7-en-24-oic Acid

3β-Hydroxy-5α-chol-7-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-8-en-24-oic Acid

3α-Hydroxy-5β-chol-8-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-8(14)-en-24-oic Acid

3α-Hydroxy-5β-chol-8(14)-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-9(11)-en-24-oic Acid

3α-Hydroxy-5β-chol-9(11)-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxy-5β-chol-9(11)-en-24-oic Acid

3β-Hydroxy-5β-chol-9(11)-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-11-en-24-oic Acid

3α-Hydroxy-5β-chol-11-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β-chol-14-en-24-oic Acid

3α-Hydroxy-5β-chol-14-en-24-oic Acid

C24H38O3 (374.2821)


   

7α-Hydroxy-5β-chol-3-en-24-oic Acid

7α-Hydroxy-5β-chol-3-en-24-oic Acid

C24H38O3 (374.2821)


   

12α-Hydroxy-5β-chol-3-en-24-oic Acid

12α-Hydroxy-5β-chol-3-en-24-oic Acid

C24H38O3 (374.2821)


   

7-Oxo-5α-cholan-24-oic Acid

7-Oxo-5α-cholan-24-oic Acid

C24H38O3 (374.2821)


   

7α-Hydroxy-5β-chol-2-en-24-oic Acid

7α-Hydroxy-5β-chol-2-en-24-oic Acid

C24H38O3 (374.2821)


   

3β-Hydroxy-5β-chol-1-en-24-oic Acid

3β-Hydroxy-5β-chol-1-en-24-oic Acid

C24H38O3 (374.2821)


   

11-Oxo-5β-cholan-24-oic Acid

11-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5β,14β-chol-8-en-24-oic Acid

3α-Hydroxy-5β,14β-chol-8-en-24-oic Acid

C24H38O3 (374.2821)


   

(20S)-3β-Hydroxychol-5-en-24-oic Acid

(20S)-3β-Hydroxychol-5-en-24-oic Acid

C24H38O3 (374.2821)


   

(20S,22E)-3β-Hydroxy-5α-chol-22-en-24-oic Acid

(20S,22E)-3β-Hydroxy-5α-chol-22-en-24-oic Acid

C24H38O3 (374.2821)


   

3α-Hydroxy-5α-chol-6-en-24-oic Acid

3α-Hydroxy-5α-chol-6-en-24-oic Acid

C24H38O3 (374.2821)


   

15-Oxo-5β-cholan-24-oic Acid

15-Oxo-5β-cholan-24-oic Acid

C24H38O3 (374.2821)


   

Cholenate

(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

C24H38O3 (374.2821)


D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts D005765 - Gastrointestinal Agents > D002793 - Cholic Acids 3b-Hydroxy-5-cholenoic acid is a monohydroxy bile acid of endogenous origin and could be found in children with the syndrome of hepatic ductular hypoplasia.

   

Ginkgolic acid 17:1

2-[(10Z)-heptadec-10-en-1-yl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


Ginkgolic acid C17:1, extracted from Ginkgo biloba Leaves, suppresses constitutive and inducible STAT3 activation through induction of PTEN and SHP-1 tyrosine phosphatase. Ginkgolic acid C17:1 has anticancer effects[1]. Ginkgolic acid C17:1, extracted from Ginkgo biloba Leaves, suppresses constitutive and inducible STAT3 activation through induction of PTEN and SHP-1 tyrosine phosphatase. Ginkgolic acid C17:1 has anticancer effects[1].

   

Merulinic acid C

2-[(8E)-heptadec-8-en-1-yl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

15-HTPE

15-hydroxy-6Z,9Z,12Z,16E,18Z-tetracosapentaenoic acid

C24H38O3 (374.2821)


   

15R-HTPE

15R-hydroxy-tetracosa-6Z,9Z,12Z,16E,18Z-pentaenoic acid

C24H38O3 (374.2821)


   

15S-HTPE

15S-hydroxy-tetracosa-6Z,9Z,12Z,16E,18Z-pentaenoic acid

C24H38O3 (374.2821)


   

1alpha,24-dihydroxy-25,26,27-trinorvitamin D3

(5Z,7E)-(1S,3R)-9,10-seco-5,7,10(19)-cholatriene-1,3,24-triol

C24H38O3 (374.2821)


   

ST 24:2;O3

(20S,22E)-3beta-Hydroxy-5alpha-chol-22-en-24-oic Acid

C24H38O3 (374.2821)


   

Drophiobiolin A

Drophiobiolin A

C24H38O3 (374.2821)


   

6-((Z)-heptadec-8-en-1-yl)salicylic acid

(Z)-2-hydroxy-6-(heptadec-8-en-1-yl)benzoic acid

C24H38O3 (374.2821)


   

(-)-N,N-(1R,2R)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE)

(-)-N,N-(1R,2R)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE)

C24H38O3 (374.2821)


   

(+)-MBF-OH dimer

(+)-MBF-OH dimer

C24H38O3 (374.2821)


   

(2R,5S)-5-AMINO-8-GUANIDINO-4-OXO-2-PHENYLMETHYLOCTANOICACIDSULFATE

(2R,5S)-5-AMINO-8-GUANIDINO-4-OXO-2-PHENYLMETHYLOCTANOICACIDSULFATE

C24H38O3 (374.2821)


   
   

Icosabutate

Icosabutate

C24H38O3 (374.2821)


C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent

   

Androstenediol 3-tetrahydropyranyl ether

Androstenediol 3-tetrahydropyranyl ether

C24H38O3 (374.2821)


   

4-(3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

4-(3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

C24H38O3 (374.2821)


   

6-((Z)-pentadec-8-en-1-yl)salicylic acid

6-((Z)-pentadec-8-en-1-yl)salicylic acid

C24H38O3 (374.2821)


   

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

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

C20H40NO5+ (374.2906)


   

3beta,21-Dihydroxy-4,4,14-trimethyl-5alpha-pregn-8-en-20-one

3beta,21-Dihydroxy-4,4,14-trimethyl-5alpha-pregn-8-en-20-one

C24H38O3 (374.2821)


   

15-hydroxy-tetracosa-6,9,12,16,18-pentaenoic acid

15-hydroxy-tetracosa-6,9,12,16,18-pentaenoic acid

C24H38O3 (374.2821)


An oxylipin that is the 15-hydoxy derivative of (6Z,9Z,12Z,16E,18Z)-tetracosa-6,9,12,16,18-pentaenoic acid. Isolated from soft cora Sinularia numerosa, it exhibits anti-angiogenic activity.

   

3alpha-Hydroxy-5beta-chol-7-en-24-oic Acid

3alpha-Hydroxy-5beta-chol-7-en-24-oic Acid

C24H38O3 (374.2821)


   

3beta-Hydroxychol-4-en-24-oic Acid

3beta-Hydroxychol-4-en-24-oic Acid

C24H38O3 (374.2821)


   

3alpha-Hydroxychol-4-en-24-oic Acid

3alpha-Hydroxychol-4-en-24-oic Acid

C24H38O3 (374.2821)


   

3alpha-Hydroxy-5beta-chol-14-en-24-oic Acid

3alpha-Hydroxy-5beta-chol-14-en-24-oic Acid

C24H38O3 (374.2821)


   

12alpha-Hydroxy-5beta-chol-3-en-24-oic Acid

12alpha-Hydroxy-5beta-chol-3-en-24-oic Acid

C24H38O3 (374.2821)


   

(20S,22E)-3beta-Hydroxy-5alpha-chol-22-en-24-oic Acid

(20S,22E)-3beta-Hydroxy-5alpha-chol-22-en-24-oic Acid

C24H38O3 (374.2821)


   

Hydroxytetracosapentaenoic acid

Hydroxytetracosapentaenoic acid

C24H38O3 (374.2821)


   

Hydroxycholenoic acid

Hydroxycholenoic acid

C24H38O3 (374.2821)


   

Oxocholanoic acid

Oxocholanoic acid

C24H38O3 (374.2821)


   

2-(heptadec-10-en-1-yl)-6-methoxycyclohexa-2,5-diene-1,4-dione

2-(heptadec-10-en-1-yl)-6-methoxycyclohexa-2,5-diene-1,4-dione

C24H38O3 (374.2821)


   

methyl 2-[(2s,6s)-6-(10-phenyldecyl)oxan-2-yl]acetate

methyl 2-[(2s,6s)-6-(10-phenyldecyl)oxan-2-yl]acetate

C24H38O3 (374.2821)


   

methyl 2-methoxy-6-(pentadec-10-en-1-yl)benzoate

methyl 2-methoxy-6-(pentadec-10-en-1-yl)benzoate

C24H38O3 (374.2821)


   

1-(3,4-dihydroxyphenyl)octadec-13-en-5-one

1-(3,4-dihydroxyphenyl)octadec-13-en-5-one

C24H38O3 (374.2821)


   

1-[(1s,3ar,5r,5ar,7s,9as,11ar)-5,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]ethanone

1-[(1s,3ar,5r,5ar,7s,9as,11ar)-5,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]ethanone

C24H38O3 (374.2821)


   

(15r,16e)-15-hydroxytetracosa-6,9,12,16,18-pentaenoic acid

(15r,16e)-15-hydroxytetracosa-6,9,12,16,18-pentaenoic acid

C24H38O3 (374.2821)


   

2-[(8z)-heptadec-8-en-1-yl]-6-hydroxybenzoic acid

2-[(8z)-heptadec-8-en-1-yl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

1-(2,6-dihydroxyphenyl)octadec-8-en-1-one

1-(2,6-dihydroxyphenyl)octadec-8-en-1-one

C24H38O3 (374.2821)


   

6-(10'z-heptadecenyl)salicylicacid

NA

C24H38O3 (374.2821)


{"Ingredient_id": "HBIN011996","Ingredient_name": "6-(10'z-heptadecenyl)salicylicacid","Alias": "NA","Ingredient_formula": "C24H38O3","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "9388","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

1-{5,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}ethanone

1-{5,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}ethanone

C24H38O3 (374.2821)


   

(10z)-1-(2,6-dihydroxyphenyl)octadec-10-en-1-one

(10z)-1-(2,6-dihydroxyphenyl)octadec-10-en-1-one

C24H38O3 (374.2821)


   

(13z)-1-(3,4-dihydroxyphenyl)octadec-13-en-5-one

(13z)-1-(3,4-dihydroxyphenyl)octadec-13-en-5-one

C24H38O3 (374.2821)


   

(1's,2r,3'as,3'br,5r,5'as,9'as,9'bs,11'ar)-1',5,9'a,11'a-tetramethyl-dodecahydrospiro[oxane-2,2'-phenanthro[1,2-b]furan]-7'-one

(1's,2r,3'as,3'br,5r,5'as,9'as,9'bs,11'ar)-1',5,9'a,11'a-tetramethyl-dodecahydrospiro[oxane-2,2'-phenanthro[1,2-b]furan]-7'-one

C24H38O3 (374.2821)


   

2-[(2r,5s)-5-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]oxan-2-yl]prop-2-enoic acid

2-[(2r,5s)-5-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]oxan-2-yl]prop-2-enoic acid

C24H38O3 (374.2821)


   

methyl 2-[6-(10-phenyldecyl)oxan-2-yl]acetate

methyl 2-[6-(10-phenyldecyl)oxan-2-yl]acetate

C24H38O3 (374.2821)


   

methyl 19-(furan-2-yl)nonadec-5-ynoate

methyl 19-(furan-2-yl)nonadec-5-ynoate

C24H38O3 (374.2821)


   

(6e,9e,12e,15r,16e,18z)-15-hydroxytetracosa-6,9,12,16,18-pentaenoic acid

(6e,9e,12e,15r,16e,18z)-15-hydroxytetracosa-6,9,12,16,18-pentaenoic acid

C24H38O3 (374.2821)


   

(4r)-4-[(1r,3as,3br,9as,9bs,11ar)-9a,11a-dimethyl-7-oxo-tetradecahydrocyclopenta[a]phenanthren-1-yl]pentanoic acid

(4r)-4-[(1r,3as,3br,9as,9bs,11ar)-9a,11a-dimethyl-7-oxo-tetradecahydrocyclopenta[a]phenanthren-1-yl]pentanoic acid

C24H38O3 (374.2821)


   

2-[(10e)-heptadec-10-en-1-yl]-6-hydroxybenzoic acid

2-[(10e)-heptadec-10-en-1-yl]-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

(2r)-2-amino-n,3-dihydroxy-n-[(10s)-10-hydroxy-3-oxohexadecyl]propanamide

(2r)-2-amino-n,3-dihydroxy-n-[(10s)-10-hydroxy-3-oxohexadecyl]propanamide

C19H38N2O5 (374.2781)


   

(1r,2r,6r,7r,8r,9r,12z)-6-isopropyl-9,13-dimethyl-3-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-12-en-9-yl butanoate

(1r,2r,6r,7r,8r,9r,12z)-6-isopropyl-9,13-dimethyl-3-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-12-en-9-yl butanoate

C24H38O3 (374.2821)


   

1-(2,6-dihydroxyphenyl)octadec-10-en-1-one

1-(2,6-dihydroxyphenyl)octadec-10-en-1-one

C24H38O3 (374.2821)


   

2-(heptadec-8-en-1-yl)-6-hydroxybenzoic acid

2-(heptadec-8-en-1-yl)-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

(3r,5s)-5-(methoxymethyl)-3-(octadeca-9,11-diyn-1-yl)oxolan-2-one

(3r,5s)-5-(methoxymethyl)-3-(octadeca-9,11-diyn-1-yl)oxolan-2-one

C24H38O3 (374.2821)


   

methyl 2-methoxy-6-[(10z)-pentadec-10-en-1-yl]benzoate

methyl 2-methoxy-6-[(10z)-pentadec-10-en-1-yl]benzoate

C24H38O3 (374.2821)


   

2-[(2r,5r)-5-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]oxan-2-yl]prop-2-enoic acid

2-[(2r,5r)-5-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]oxan-2-yl]prop-2-enoic acid

C24H38O3 (374.2821)


   

2-(heptadec-10-en-1-yl)-6-hydroxybenzoic acid

2-(heptadec-10-en-1-yl)-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

5'-ethenyl-2,5,5,5',8a-pentamethyl-4a,6,7,8-tetrahydro-4h-spiro[naphthalene-1,2'-oxolan]-4-yl butanoate

5'-ethenyl-2,5,5,5',8a-pentamethyl-4a,6,7,8-tetrahydro-4h-spiro[naphthalene-1,2'-oxolan]-4-yl butanoate

C24H38O3 (374.2821)


   

(1r,4s,4as,5's,8as)-5'-ethenyl-2,5,5,5',8a-pentamethyl-4a,6,7,8-tetrahydro-4h-spiro[naphthalene-1,2'-oxolan]-4-yl butanoate

(1r,4s,4as,5's,8as)-5'-ethenyl-2,5,5,5',8a-pentamethyl-4a,6,7,8-tetrahydro-4h-spiro[naphthalene-1,2'-oxolan]-4-yl butanoate

C24H38O3 (374.2821)


   

2-(heptadec-1-en-1-yl)-6-hydroxybenzoic acid

2-(heptadec-1-en-1-yl)-6-hydroxybenzoic acid

C24H38O3 (374.2821)


   

1',5,9'a,11'a-tetramethyl-dodecahydrospiro[oxane-2,2'-phenanthro[1,2-b]furan]-7'-one

1',5,9'a,11'a-tetramethyl-dodecahydrospiro[oxane-2,2'-phenanthro[1,2-b]furan]-7'-one

C24H38O3 (374.2821)


   

methyl 2-methoxy-6-(pentadec-8-en-1-yl)benzoate

methyl 2-methoxy-6-(pentadec-8-en-1-yl)benzoate

C24H38O3 (374.2821)


   

4-hydroxy-5-methyl-3-(13-phenyltridecyl)oxolan-2-one

4-hydroxy-5-methyl-3-(13-phenyltridecyl)oxolan-2-one

C24H38O3 (374.2821)


   

6-[(2e,4e,8e,10e)-6,8-dimethylpentadeca-2,4,8,10,14-pentaen-1-yl]-2,3-dimethyloxane-2,4-diol

6-[(2e,4e,8e,10e)-6,8-dimethylpentadeca-2,4,8,10,14-pentaen-1-yl]-2,3-dimethyloxane-2,4-diol

C24H38O3 (374.2821)


   

methyl 2-methoxy-6-[(8z)-pentadec-8-en-1-yl]benzoate

methyl 2-methoxy-6-[(8z)-pentadec-8-en-1-yl]benzoate

C24H38O3 (374.2821)


   

{14-ethoxy-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-11-en-5-yl}methyl acetate

{14-ethoxy-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-11-en-5-yl}methyl acetate

C24H38O3 (374.2821)


   

(8z)-1-(2,6-dihydroxyphenyl)octadec-8-en-1-one

(8z)-1-(2,6-dihydroxyphenyl)octadec-8-en-1-one

C24H38O3 (374.2821)


   

[(1s,4s,5s,9r,10r,13s,14r)-14-ethoxy-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-11-en-5-yl]methyl acetate

[(1s,4s,5s,9r,10r,13s,14r)-14-ethoxy-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-11-en-5-yl]methyl acetate

C24H38O3 (374.2821)


   

2-[(10e)-heptadec-10-en-1-yl]-6-methoxycyclohexa-2,5-diene-1,4-dione

2-[(10e)-heptadec-10-en-1-yl]-6-methoxycyclohexa-2,5-diene-1,4-dione

C24H38O3 (374.2821)