Exact Mass: 402.2769948
Exact Mass Matches: 402.2769948
Found 500 metabolites which its exact mass value is equals to given mass value 402.2769948,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Gamabufogenin
Gamabufogenin is a steroid lactone. It is functionally related to a bufanolide. Gamabufotalin is a natural product found in Bufotes viridis, Bufo, and other organisms with data available. D020011 - Protective Agents > D002316 - Cardiotonic Agents > D002301 - Cardiac Glycosides D020011 - Protective Agents > D002316 - Cardiotonic Agents > D002018 - Bufanolides Gamabufotalin (Gamabufagin), a main active compound isolated from Chinese medicine Chansu, has been shown to strongly inhibit cancer cell growth and inflammatory response. Gamabufotalin could inhibite angiogenesis by inhibiting the activation of VEGFR-2 signaling pathways. Gamabufotalin (Gamabufagin), a main active compound isolated from Chinese medicine Chansu, has been shown to strongly inhibit cancer cell growth and inflammatory response. Gamabufotalin could inhibite angiogenesis by inhibiting the activation of VEGFR-2 signaling pathways.
Telobufotoxin
Telocinobufagin is a steroid lactone. It is functionally related to a bufanolide. Telocinobufagin is a natural product found in Bufo gargarizans, Bufo bufo, and other organisms with data available. D020011 - Protective Agents > D002316 - Cardiotonic Agents > D002301 - Cardiac Glycosides D020011 - Protective Agents > D002316 - Cardiotonic Agents > D002018 - Bufanolides Telocinobufagin is one of anti-hepatoma constituent in Venenum Bufonis. Telocinobufagin is one of anti-hepatoma constituent in Venenum Bufonis.
ST 24:4;O5
C78276 - Agent Affecting Digestive System or Metabolism > C66913 - Cholagogues or Choleretic Agents D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts D005765 - Gastrointestinal Agents > D002793 - Cholic Acids Same as: D01693
Sorbitan palmitate
Sorbitan palmitate is a food emulsifier, stabilise Food emulsifier, stabiliser
Merodesmosine
Aminoacid from reduced elastin. Merodesmosine is found in animal foods. Merodesmosine is found in animal foods. Aminoacid from reduced elasti
Lucidone A
Lucidone A is found in mushrooms. Lucidone A is a constituent of Ganoderma lucidum (reishi)
7b-Hydroxy-3-oxo-5b-cholanoic acid
7b-Hydroxy-3-oxo-5b-cholanoic acid was one of the bile acids present in significant proportions during early gestation, identified in amniotic fluid. (PMID 2373959). A bile acid. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending 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). 7b-Hydroxy-3-oxo-5b-cholanoic acid was one of the bile acids present in significant proportions during early gestation, identified in amniotic fluid. (PMID 2373959).
MG(0:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0)
MG(0:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well. [HMDB] MG(0:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well.
MG(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0/0:0)
MG(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well.
Androstenediol dipropionate
Gamabufotalin
l-lysyl-l-lysyl-l-lysine
Telocinobufagin
Clascoterone
C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C146993 - Androgen Receptor Inhibitor D - Dermatologicals > D10 - Anti-acne preparations > D10A - Anti-acne preparations for topical use C147908 - Hormone Therapy Agent > C547 - Hormone Antagonist > C242 - Anti-Androgen
Ardisiphenol C
An acetate ester obtained from the formal condensation of acetic acid with the hydroxy group at position 1 of 6-[(8Z,11Z)-heptadeca-8,11-dien-1-yl]benzene-1,2,4-triol. Isolated from the dried fruits of Ardisia colorata, it exhibits scavenging activity towards DPPH radicals and cytotoxicity against murine breast cancer cell line, FM3A.
17-Succinoyloxy-ent-cleroda-3,13(16),14-trien-15,16-oxide
16,25-Dihydroxy-13(24),17-cheilanthadien-19,25-olide
3alpha,14alpha-Diacetoxy-2beta-hydroxy-1(15),8(19),9-trinervitatriene
UNII:GE16EV367Q
CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10670; ORIGINAL_PRECURSOR_SCAN_NO 10667 CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10650; ORIGINAL_PRECURSOR_SCAN_NO 10647 CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10686; ORIGINAL_PRECURSOR_SCAN_NO 10684 CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10720; ORIGINAL_PRECURSOR_SCAN_NO 10719 CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10714; ORIGINAL_PRECURSOR_SCAN_NO 10712 DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; ORIGINAL_ACQUISITION_NO 10701; ORIGINAL_PRECURSOR_SCAN_NO 10700 CONFIDENCE standard compound; INTERNAL_ID 847; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10701; ORIGINAL_PRECURSOR_SCAN_NO 10700
3alpha,9,14-Trihydroxy-5beta,14beta-bufa-20,22-dienolid|3alpha,9,14-trihydroxy-5beta,14beta-bufa-20,22-dienolide
8-(15-hydroxypentadecyl)-7-methoxy-2h-benzopyran-2-one
1beta,11alpha-Diacetoxy-7-oxosandaracopimar-8(14),15-dien
15alpha-isovaleroyloxy-ent-kaurenic acid|15alpha-isovaleroyloxykaur-16-en-19-oic acid|grandifloric acid isovalerate
19-Carboxylic acid,3-(3-methylbutanoyl)-(ent-3beta)-16-Kaurene-3,19-diol|19-Carboxylic acid,O-(3-methylbutanoyl)-(ent-3beta)-16-Kaurene-3,19-diol
12-O-deacetyl-12-epi-19-deoxy-21-hydroxyscalarin
A scalarane sesterterpenoid that is 12-O-deacetyl-12-epi-19-deoxy-scalarin substituted by an additional hydroxy group at position 21. It has been isolated from the sponge, Hyattella species.
(2R)-2-{(1S,2S)-1,2-dihydroxy-8-[(2R,3R,4R,5R)-5-(2-hydroxymethyl-3,4-dihydroxy-1-acetylpyrrolidinyl)]octyl}piperidine|broussonetine J1
3beta,6alpha-dihydroxy-5-alpha-pregna-20-en-3,6-diacetate|ximaosteroid B
7-(3-methylbutyroxy)cleisthanth-13,15-dien-18-oic acid
(2Z)-3-methyl-5-{(1S,2R,4R,4aR,8aR)-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a,5-tetramethyl-4-{[(2Z)-2-methyl-1-oxo-but-2-en-1-yl]oxy}naphthalen-1-yl}pent-2-enoic acid|solidagocanin B
7beta-angeloyloxy-8alpha-isobutyryloxylongipin-2-en-1-one
(ent-15beta)-2-Methylbutanoyl-15-Hydroxy-16-kauren-19-oic acid|2-Methylbutanoyl-15-Hydroxy-16-kauren-19-oic acid
4-hydroxy-6-ethoxy-2-[(10Z,13Z)-10,13,16-heptadecatriene]resorcinol
18R,20-dihydroxy-2,10,19(21)-cladocoratrien-22(20)-olide|cladocoran B
ent-15alpha-angeloyloxy-16beta,17-epoxykauran-3beta-ol
2-oxo-18,19-diacetoxy-10alpha,17alpha,19alpha,20beta-(-)-cleroda-3,13(16),14-triene
(ent-15beta)-3-Methylbutanoyl-15-Hydroxy-16-kauren-19-oic acid|3-Methylbutanoyl-15-Hydroxy-16-kauren-19-oic acid
(-)-(5E,12E,2S,3S,4S,9S,11S,15R)-3,15-diacetoxylathyra-5,12-dien-14-one|3beta,15beta-diacetoxylathyra-5E,12E-dien-14-one|jolkinoate A
(2E,4E,6E)-6-(1-carboxyocta-2,4,6-triene)-11,12-epoxy-9-hydroxy-11-methoxy-drim-7-ene
6-O-alpha-E-p-coumaroyl-1beta,4alpha-dihydroxyeudesmane
14-[(2-methylbutanoyl)oxy]-3,4-seco-ent-kaura-4(19),16-dien-3-oic acid
ent-3beta-(3-methyl-2-butanoyloxy)-15-beyeren-19-oic acid
2alpha-isobutyryloxy-15,16-epoxylabda-7,13(16),14-trien-18-oic acid
rel-(3S,1R,2S)-3-(1-farnesyl-2-hydroxy-4-oxocyclopentan-1-yl)-3-ethoxypropanoic acid lactone
18-(2-Methylbutanoyl) 鈥樎?ent-3beta,4alphaH)-15,16-Epoxy-7,13(16),14-clerodatriene-3,18-diol
2-acetyl-3,5-dihydroxy-1-geranoxy-6-methyl-4-(2-methyl)butyryl-benzene
hexanocucurbitacin D|Hexanor-cucurbitacin D|Hexanorcucurbitacin D
(3beta,4beta,5beta,14beta)-3,4,14-Trihydroxybufa-20,22-dienolide
Di-Ac-7, 8-Epoxy-3, 12(18), 13-dolabellatriene-19, 20-diol
(1S,2R,3E,7E,11S,12R,13S)-2,13-diacetoxydolabella-3,7,18-trien-9-one
7alpha-hydroxy-8,11,13-abietatriene-18-succinic acid|abiesadine F
6alpha,12-diacetoxy-7beta-hydroxyabieta-8,11,13-triene|fortunin B
12beta-Hydroxy-(3beta,20S)-3-Hydroxy-4,4,14-trimethylpregna-7,9(11)-diene-20-carboxylic acid
Vibsanin A
Hexanorcucurbitacin D
hexanorcucurbitacin D is a natural product found in Begonia parviflora, Cucumis melo, and other organisms with data available.
Dehydrocholic acid
Dehydrocholic acid is a synthetic bile acid, manufactured by the oxidation of cholic acid. It acts as a hydrocholeretic, increasing bile output to clear increased bile acid load. 3,7,12-trioxo-5beta-cholanic acid is an oxo-5beta-cholanic acid in which three oxo substituents are located at positions 3, 7 and 12 on the cholanic acid skeleton. It has a role as a gastrointestinal drug. It is an oxo-5beta-cholanic acid, a 7-oxo steroid, a 12-oxo steroid and a 3-oxo-5beta-steroid. It is a conjugate acid of a 3,7,12-trioxo-5beta-cholan-24-oate. Dehydrocholic acid is a synthetic bile acid that was prepared from the oxidation of cholic acid with chromic acid. It has been used for stimulation of biliary lipid secretion. The use of dehydrocholic acid in over-the-counter products has been discontinued by Health Canada.
(4R)-4-[(5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3,7,12-trioxo-1,2,4,5,6,8,9,11,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pentanoic acid
Sorbitane Monopalmitate - Polysorbate 40 in-source fragment
C25H38O4_(5xi,9xi)-Beyer-15-en-18-yl methyl succinate
C25H38O4_(3aR,5E,7S,10E,14E,16aS)-2,7-Dihydroxy-3-[(2S)-1-hydroxy-2-propanyl]-6,10,14,16a-tetramethyl-4,7,8,9,12,13,16,16a-octahydrocyclopenta[15]annulen-1(3aH)-one
3,7,12-Trioxo-5b-cholan-24-oic acid
BA-119-90. 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-119-60. 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-119-30. 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.
3,7,12-Trioxo-5a-cholan-24-oic acid
BA-128-120. 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-128-90. 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-128-60. 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.
bis(2-butoxyethyl) sebacate
CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10403; ORIGINAL_PRECURSOR_SCAN_NO 10399 CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10586; ORIGINAL_PRECURSOR_SCAN_NO 10583 CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10430; ORIGINAL_PRECURSOR_SCAN_NO 10428 CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10635; ORIGINAL_PRECURSOR_SCAN_NO 10632 CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10667; ORIGINAL_PRECURSOR_SCAN_NO 10663 CONFIDENCE standard compound; INTERNAL_ID 891; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10506; ORIGINAL_PRECURSOR_SCAN_NO 10503
1-methyl 4-[(5R,9S,13S)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl butanedioate_major
methyl (4R)-4-((5R,8S,9S,10R,13R,17R)-10,13-dimethyl-3,6-dioxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
Ala Gly Lys Lys
Ala Ile Ile Ser
Ala Ile Leu Ser
Ala Ile Ser Ile
Ala Ile Ser Leu
Ala Ile Thr Val
Ala Ile Val Thr
Ala Lys Gly Lys
Ala Lys Lys Gly
Ala Leu Ile Ser
Ala Leu Leu Ser
Ala Leu Ser Ile
Ala Leu Ser Leu
Ala Leu Thr Val
Ala Leu Val Thr
Pregn-4-ene-3,20-dione, 6a,17-dihydroxy-6-methyl-, 17-acetate
Pregn-4-ene-3,20-dione, 6b,17-dihydroxy-6-methyl-, 17-acetate
7,21-Dihydroxy-6a-methylpregn-4-ene-3,20-dione 17-acetate
Ala Ser Ile Ile
Ala Ser Ile Leu
Ala Ser Leu Ile
Ala Ser Leu Leu
Ala Thr Ile Val
Ala Thr Leu Val
Ala Thr Val Ile
Ala Thr Val Leu
Ala Val Ile Thr
Ala Val Leu Thr
Ala Val Thr Ile
Ala Val Thr Leu
Gly Ala Lys Lys
Gly Ile Ile Thr
Gly Ile Leu Thr
Gly Ile Thr Ile
Gly Ile Thr Leu
Gly Lys Ala Lys
Gly Lys Lys Ala
Gly Leu Ile Thr
Gly Leu Leu Thr
Gly Leu Thr Ile
Gly Leu Thr Leu
Gly Thr Ile Ile
Gly Thr Ile Leu
Gly Thr Leu Ile
Gly Thr Leu Leu
Ile Ala Ile Ser
Ile Ala Leu Ser
Ile Ala Ser Ile
Ile Ala Ser Leu
Ile Ala Thr Val
Ile Ala Val Thr
Ile Gly Ile Thr
Ile Gly Leu Thr
Ile Gly Thr Ile
Ile Gly Thr Leu
Ile Ile Ala Ser
Ile Ile Gly Thr
Ile Ile Ser Ala
Ile Ile Thr Gly
Ile Leu Ala Ser
Ile Leu Gly Thr
Ile Leu Ser Ala
Ile Leu Thr Gly
Ile Ser Ala Ile
Ile Ser Ala Leu
Ile Ser Ile Ala
Ile Ser Leu Ala
Ile Thr Ala Val
Ile Thr Gly Ile
Ile Thr Gly Leu
Ile Thr Ile Gly
Ile Thr Leu Gly
Ile Thr Val Ala
Ile Val Ala Thr
Ile Val Thr Ala
Lys Ala Gly Lys
Lys Ala Lys Gly
Lys Gly Ala Lys
Lys Gly Lys Ala
Lys Lys Ala Gly
Lys Lys Gly Ala
Leu Ala Ile Ser
Leu Ala Leu Ser
Leu Ala Ser Ile
Leu Ala Ser Leu
Leu Ala Thr Val
Leu Ala Val Thr
Leu Gly Ile Thr
Leu Gly Leu Thr
Leu Gly Thr Ile
Leu Gly Thr Leu
Leu Ile Ala Ser
Leu Ile Gly Thr
Leu Ile Ser Ala
Leu Ile Thr Gly
Leu Leu Ala Ser
Leu Leu Gly Thr
Leu Leu Ser Ala
Leu Leu Thr Gly
Leu Ser Ala Ile
Leu Ser Ala Leu
Leu Ser Ile Ala
Leu Ser Leu Ala
Leu Thr Ala Val
Leu Thr Gly Ile
Leu Thr Gly Leu
Leu Thr Ile Gly
Leu Thr Leu Gly
Leu Thr Val Ala
Leu Val Ala Thr
Leu Val Thr Ala
Ser Ala Ile Ile
Ser Ala Ile Leu
Ser Ala Leu Ile
Ser Ala Leu Leu
Ser Ile Ala Ile
Ser Ile Ala Leu
Ser Ile Ile Ala
Ser Ile Leu Ala
Ser Leu Ala Ile
Ser Leu Ala Leu
Ser Leu Ile Ala
Ser Leu Leu Ala
Ser Val Val Val
Thr Ala Ile Val
Thr Ala Leu Val
Thr Ala Val Ile
Thr Ala Val Leu
Thr Gly Ile Ile
Thr Gly Ile Leu
Thr Gly Leu Ile
Thr Gly Leu Leu
Thr Ile Ala Val
Thr Ile Gly Ile
Thr Ile Gly Leu
Thr Ile Ile Gly
Thr Ile Leu Gly
Thr Ile Val Ala
Thr Leu Ala Val
Thr Leu Gly Ile
Thr Leu Gly Leu
Thr Leu Ile Gly
Thr Leu Leu Gly
Thr Leu Val Ala
Thr Val Ala Ile
Thr Val Ala Leu
Thr Val Ile Ala
Thr Val Leu Ala
Val Ala Ile Thr
Val Ala Leu Thr
Val Ala Thr Ile
Val Ala Thr Leu
Val Ile Ala Thr
Val Ile Thr Ala
Val Leu Ala Thr
Val Leu Thr Ala
Val Ser Val Val
Val Thr Ala Ile
Val Thr Ala Leu
Val Thr Ile Ala
Val Thr Leu Ala
Val Val Ser Val
Val Val Val Ser
1α-hydroxy-26,27-dinorvitamin D3 25-carboxylic acid / 1α-hydroxy-26,27-dinorcholecalciferol 25-carboxylic acid
methyl ester
lucidone A
methyl (((4R,9S,11bS)-4,9,11b-trimethyl-1,2,3,4,4a,5,6,9,10,11,11a,11b-dodecahydro-6a,9-methanocyclohepta[a]naphthalen-4-yl)methyl) succinate
ascr#28
An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (15R)-15-hydroxypalmitic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
oscr#28
An omega-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of 16-hydroxyhexadecanoic acid (also known as juniperic acid) with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
1alpha-hydroxy-26,27-dinorvitamin D3 25-carboxylic acid / 1alpha-hydroxy-26,27-dinorcholecalciferol 25-carboxylic acid
Hyrtios sesterterpene 1
(2E,5E)-2,5-BIS[(4-(DIETHYLAMINO)PHENYL)METHYLENE]CYCLOPENTANONE
DI-2-ETHYLHEXYL 3,3-THIODIPROPIONATE
C22H42O4S (402.28036520000006)
4,4-di(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b]dithiophene
Bepridil hydrochloride
D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D000077264 - Calcium-Regulating Hormones and Agents D049990 - Membrane Transport Modulators
ALPHA,ALPHA-BIS(4-HYDROXY-3,5-DIMETHYLPHENYL)-1,4-DIISOPROPYLBENZENE
17α-hydroxy-19-norpregna-5(10),9(11)-diene-3,20-dione 3,20-bis(ethylene acetal)
3,6-Dioxo-5β-24-cholanoic acid methyl ester
1,1-[Methylenebis(4,1-phenyleneoxy)]bis[3-(ethylamino)-2-propanol]
C23H34N2O4 (402.25184440000004)
(1S,3R,7S,8S,8aR)-1,2,3,7,8,8a-Hexahydro-3,7-diMethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl Ester (2Z)-2-Methyl-2-butenoic Acid
Poly(hexamethylenebicyanoguanide-hexamethylenediamine) hydrochloride
2,3-dihydroxypropyl (4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoate
16-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]hexadecanoic acid
4-(cyclopropylmethyl)-1-(1H-pyrrolo[2,3-c]pyridin-3-ylmethyl)spiro[3,5-dihydro-1,4-benzoxazepine-2,4-piperidine]
[3-Carboxy-2-(13-carboxytridecanoyloxy)propyl]-trimethylazanium
C21H40NO6+ (402.28554800000006)
Sesterstatin 2
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
Sesterstatin 3
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
Sesterstatin 1
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
(1R,3Z,5S,8Z,12Z,15S)-5,17-dihydroxy-18-[(2S)-1-hydroxypropan-2-yl]-4,8,12,15-tetramethylbicyclo[13.3.0]octadeca-3,8,12,17-tetraen-16-one
(2S)-6-amino-2-[[(2S)-5-amino-2-[[(2S)-2,6-diaminohexanoyl]amino]-5-oxopentanoyl]amino]hexanoic acid
Ala-Leu-Leu-Ser
A tetrapeptide composed of L-alanine, two L-leucine units, and L-serine joined in sequence by peptide linkages.
1-[4-(2,3-Dimethylphenyl)piperazin-1-yl]-3-(4,4,6-trimethyl-2-sulfanylidene-1,3-diazinan-1-yl)propan-1-one
3-(17-hydroxy-10,13-dimethyl-3-oxo-7-propyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)propanoic acid
(15S)-15alpha-(Isovaleryloxy)kaur-16-en-18-oic acid
15-[(2R,3R,5R,6S)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-3-oxopentadecanoic acid
(14R)-14-[(2R,3R,5R,6S)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-3-oxopentadecanoic acid
N-benzyl-N-[3-(2-methylpropoxy)-2-(pyrrolidin-1-yl)propyl]aniline hydrochloride
(1R,3E,5S,8Z,12E,15S)-5,17-Dihydroxy-18-[(2S)-1-hydroxypropan-2-yl]-4,8,12,15-tetramethylbicyclo[13.3.0]octadeca-3,8,12,17-tetraen-16-one
[(2R)-3-carboxy-2-(13-carboxytridecanoyloxy)propyl]-trimethylazanium
C21H40NO6+ (402.28554800000006)
(5E,10E,14Z)-2,7-Dihydroxy-3-(2-hydroxy-1-methylethyl)-6,10,14,16a-tetramethyl-3a,7,8,9,12,13,16,16a-octahydrocyclopentacyclopentadecen-1(4H)-one
(1R,3E,5S,15S)-5,17-dihydroxy-18-[(2S)-1-hydroxypropan-2-yl]-4,8,12,15-tetramethylbicyclo[13.3.0]octadeca-3,8,12,17-tetraen-16-one
[(2S)-2,3-dihydroxypropyl] (4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoate
[1-carboxy-3-[2-hydroxy-3-[(E)-undec-4-enoyl]oxypropoxy]propyl]-trimethylazanium
C21H40NO6+ (402.28554800000006)
16-O-deacetyl-16-epi-scalarolbutenolide
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus that exhibits antineoplastic activity.