Exact Mass: 514.3294215999999
Exact Mass Matches: 514.3294215999999
Found 500 metabolites which its exact mass value is equals to given mass value 514.3294215999999,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
elatericin B
Cucurbitacin I is a cucurbitacin that is 9,10,14-trimethyl-4,9-cyclo-9,10-secocholesta-2,5,23-triene substituted by hydroxy groups at positions 2, 16, 20 and 25 and oxo groups at positions 1, 11 and 22. It has a role as a plant metabolite and an antineoplastic agent. It is a cucurbitacin and a tertiary alpha-hydroxy ketone. Cucurbitacin I is a natural product found in Elaeocarpus chinensis, Elaeocarpus hainanensis, and other organisms with data available. A cucurbitacin that is 9,10,14-trimethyl-4,9-cyclo-9,10-secocholesta-2,5,23-triene substituted by hydroxy groups at positions 2, 16, 20 and 25 and oxo groups at positions 1, 11 and 22. Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity.
stigmatellin
A member of the class of chromones that is isolated from Stigmatella aurantiaca Sg a15. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents
Ganoderic acid J
Ganoderic acid J is found in mushrooms. Ganoderic acid J is a metabolite of Ganoderma lucidum (reishi).
Ganoderenic acid B
Ganoderenic acid B is found in mushrooms. Ganoderenic acid B is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderenic acid B is found in mushrooms. Ganoderenic acid B is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderenic acid B exhibits potent reversal effect on ABCB1-mediated multidrug resistance of HepG2/ADM cells to Doxorubicin[1].
Ganoderic acid C1
Ganoderic acid C1 is found in mushrooms. Ganoderic acid C1 is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid C1 is found in mushrooms. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2].
Ganoderenic acid A
Ganoderenic acid A is found in mushrooms. Ganoderenic acid A is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderenic acid A is found in mushrooms. Ganoderenic acid A is a lanostane-type triterpene. Ganoderenic acid A is a potent inhibitor of β-glucuronidase. Ganoderenic acid A has a potent hepatoprotective effect against CCl4-induced liver injury[1]. Ganoderenic acid A is a lanostane-type triterpene. Ganoderenic acid A is a potent inhibitor of β-glucuronidase. Ganoderenic acid A has a potent hepatoprotective effect against CCl4-induced liver injury[1].
Ganoderic acid xi
Ganoderic acid xi is found in mushrooms. Ganoderic acid xi is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid xi is found in mushrooms.
Flavidulol C
Flavidulol C is found in mushrooms. Flavidulol C is isolated from the edible, but bitter tasting Japanese kihatsudake mushroom (Lactarius flavidulus). Isolated from the edible, but bitter tasting Japanese kihatsudake mushroom (Lactarius flavidulus). Flavidulol C is found in mushrooms.
Ganoderic acid V1
Ganoderic acid V1 is found in mushrooms. Ganoderic acid V1 is a metabolite of Ganoderma lucidum (reishi). Metabolite of Ganoderma lucidum (reishi). Ganoderic acid V1 is found in mushrooms.
Oleanderolide 3-acetate
Oleanderolide 3-acetate is found in fruits. Oleanderolide 3-acetate is a constituent of Rhodomyrtus tomentosa (hill gooseberry) Constituent of Rhodomyrtus tomentosa (hill gooseberry). Oleanderolide 3-acetate is found in fruits.
Ganosporelactone B
Ganosporelactone B is found in mushrooms. Ganosporelactone B is isolated from the spores of Ganoderma lucidum (reishi).
Tsugaric acid C
Tsugaric acid C is found in mushrooms. Tsugaric acid C is a constituent of Ganoderma tsugae (red reishi) Constituent of Ganoderma tsugae (red reishi). Tsugaric acid C is found in mushrooms.
16-Acetylpriverogenin A
Sapogenin from Primula veris (cowslip). 16-Acetylpriverogenin A is found in tea and herbs and spices. 16-Acetylpriverogenin A is found in herbs and spices. Sapogenin from Primula veris (cowslip
N-Docosahexaenoyl Tryptophan
N-docosahexaenoyl tryptophan belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Docosahexaenoyl amide of Tryptophan. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Docosahexaenoyl Tryptophan is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Docosahexaenoyl Tryptophan is therefore classified as a very long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.
[1-(3,3-Dimethyloxiran-2-yl)-3-[(8S,10S,11S,14R)-11-hydroxy-4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]butyl] acetate
Cucurbitacin I
Ganoderic acid D
Ganoderic acid C1 is a triterpenoid. Ganoderic acid C1 is a natural product found in Ganoderma lucidum with data available. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2].
3-O-Acetyl-16α-hydroxytrametenolic acid
3-O-Acetyl-16α-hydroxytrametenolic acid (Compound 3) is a triterpene found in Poria cocos, with anti-oxidant and anti-cancer activity[1].
23-acetate
Alisol b acetate is a triterpenoid. Alisol B 23-acetate is a natural product found in Alisma, Alisma plantago-aquatica, and other organisms with data available. See also: Alisma plantago-aquatica subsp. orientale root (part of). Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors. Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors.
Alisol
Alisol b acetate is a triterpenoid. Alisol B 23-acetate is a natural product found in Alisma, Alisma plantago-aquatica, and other organisms with data available. See also: Alisma plantago-aquatica subsp. orientale root (part of). Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors. Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors.
3-O-Acetyl-1α-hydroxytrametenolic
3-O-Acetyl-16α-hydroxytrametenolic acid (Compound 3) is a triterpene found in Poria cocos, with anti-oxidant and anti-cancer activity[1].
Laulimalide
A macrolide with formula C30H42O7 that is isolated from the marine sponges, Cacospongia mycofijiensis and Hyattella sp.
3alpha-Acetoxy-27-hydroxylup-20(29)-en-24-oic acid
Alisol B acetate
Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors. Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors.
3beta-Acetoxy-18alpha-hydroperoxy-12-oleanen-11-one
Rubiarbonone C
A pentacyclic triterpenoid of the class of arborinane-type terpenoids isolated from the roots of Rubia yunnanensis.
Ganoderic acid D
Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2]. Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2].
Anhydrocochlioquinone A
[Raw Data] CBA28_Anhydrocochlioq_pos_50eV_1-2_01_1556.txt [Raw Data] CBA28_Anhydrocochlioq_pos_40eV_1-2_01_1555.txt [Raw Data] CBA28_Anhydrocochlioq_pos_30eV_1-2_01_1554.txt [Raw Data] CBA28_Anhydrocochlioq_pos_20eV_1-2_01_1553.txt [Raw Data] CBA28_Anhydrocochlioq_pos_10eV_1-2_01_1541.txt
(17R,20S,22R)-4beta-hydroxy-1-oxo-5beta,6beta-epoxy-16alpha-acetoxywitha-2-enolide
Lanost-9(11)-en-18-oic acid, 23-(acetyloxy)-3,20-dihydroxy-, .gamma.-lactone, (3.beta.,20.xi.)-
3alpha-hydroxy-lup-20(29)-ene-23,28-dioic acid dimethyl ester|3alpha-hydroxylup-20(29)-ene-23,28-dioic acid dimethyl ester
3-acetylmaslinic acid (TARB-2)|3-O-acetylmaslinic acid
3beta-O-(beta-D-sarmentosyl)-8,14-epoxy-5beta,14beta-card-16,20(22)-dienolide|cardenolide N-2
(2I<<,3EC)- 2-(Acetyloxy)-3-hydroxy- olean-12-en-28-oic acid
Cucurbitacin I
Cucurbitacin i is a member of the class of compounds known as cucurbitacins. Cucurbitacins are polycyclic compounds containing the tetracyclic cucurbitane nucleus skeleton, 19-(10->9b)-abeo-10alanost-5-ene (also known as 9b-methyl-19-nor lanosta-5-ene), with a variety of oxygenation functionalities at different positions. Cucurbitacin i is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Cucurbitacin i can be found in cucumber, which makes cucurbitacin i a potential biomarker for the consumption of this food product. Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity.
1,3,7-Trihydroxy-3,7-dimethyl-2-(3-methylbutanoyl)-6,6-diprenyl-2,3,3a,4,7,7a-hexahydrospiro[1-cyclohexene-4,5(6H)-[1H]indene]-3,5-dione
7??,23?鈥?Dihydroxy-3,11,15-trioxolanosta-8,20E(22)-dien-26-oic acid
(22S,24S)-16,24;22,25-dianhydro-16,22,22,24,25-pentahydroxy-2beta-methoxy-3,11-dioxocucurbit-5-ene
Tetra-Ac-(2R,3S,4R)-1,2,3,4-Eicosanetetrol|Tetra-Ac-(2S,3R,4R)-1,2,3,4-Eicosanetetrol|Tetra-Ac------(2S,3S,4R)-1,2,3,4-Eicosanetetrol
methyl 7beta-hydroxy-3,11,15,23-tetraoxo-5alpha-lanost-8-en-26-oate
3beta-acetoxy-16alpha-hydroxyoleanane-13beta,28-olide
Di-Me ester-3-Hydroxy-3,4-seco-4(24),12-oleanadiene-23,28-dioic acid
(5alpha,6beta,18S,22R)-18,20-epoxy-6,22-dihydroxy-5,18-dimethoxy-1-oxoergosta-2,24-dien-26-oic acid delta-lactone|5-O-methoxywithaphysalin R
2-O-acetylcorosolic acid|2alpha,3alpha-diacetoxyurs-12-en-28-oic acid
3,7,11,15,23-pentaoxolanostan-26-oic acid|8beta,9alpha-dihydroganoderic acid C
(17R,20S,22R)-4beta-hydroxy-1-oxo-5beta,6beta-epoxy-18-acetoxywitha-2-enolide
3beta-(acetyloxy)-12beta,13-dihydroxyursan-28-oic acid gamma-lactone|3beta-acetoxy-12beta-hydroxyurs-28,13-olide
3??-Methoxy-16??-hydroxyursa-12,19(29)-dien-27,28-dioic acid
(3beta,15alpha)-3-(acetyloxy)-15-hydroxylanosta-8,24-dien-21-oic acid
2alpha,3beta-dihydroxy-urs-12,19(29)-dien-28-oic acid|euscaphic acid J
(3beta,7beta)-ergost-5,24(28)-diene-3beta,7beta,19-triol 7,19-diacetate
12-O-tiglyl-4-deoxy-4alpha-phorbol-13-(2-methyl)butyrate
(24E,3alpha,22alpha)-3-hydroxy-22-acetoxylanosta-8,24-dien-26-oic acid|astraodoric acid D
(20R)-5alpha-pregnane-2alpha,3alpha,16beta,20-tetrol 2-O-beta-D-glucopyranoside
Methyl (24E)-9??,23??-dihydroxy-3,15-dioxo-17,15-friedo-lanostan-8(14),24-dien-26-oate
3-O-Acetyl-11-hydroxy-beta-boswellic acid
3-O-acetyl-11-hydroxy-beta-boswellic acid is a natural product found in Boswellia sacra with data available. 3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor[1]. 3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor[1].
(25R)-3,4-seco-9beta-lanosta-4(28),7-dien-23-one-3,26-dioic acid dimethyl ester
3beta(H)-1-oxo-7beta,9alpha,13-triangelyloxylongipinane
3beta-acetoxy-19alpha-hydroxyurs-12-en-29beta-oic acid|acetylbignonic acid
1beta,2alpha-dihydroxy-3beta-acetoxy-11-oxours-12-ene
Rubiarbonone A
A pentacyclic triterpenoid of the class of arborinane-type terpenoids isolated from the roots of Rubia yunnanensis.
25xi,26-Dihydro,23-Ac-(3beta,23xi)-Holosta-8,25-dien-3-ol
3beta-acetoxy-11alpha,28-dihydroxy-16-oxo-12-oleanene
3beta-acetoxy-6beta-hydroxyolean-12-en-27-oic acid
2,3-seco-22,29-lactone-oleane-12-ene-2,3-dioic acid 3-methyl ester
eudesm-11-en-4alpha-O-beta-D-2-cinnamoyloxy-glucopyranoside|fissipallin
(3beta,5beta,6beta,18S,22R)-5,6:18,20-diepoxy-22-hydroxy-3,18-dimethoxy-1-oxoergost-24-en-26-oic acid delta-lactone|withaphysalin Q
(4aR)-9-((1S)-2cF-Acetoxy-1rF,3tF-dimethyl-pent-catF-yl)-3t-(alpha-hydroxy-isopropyl)-6a,12b-dimethyl-(4ar,6at,12bt)-1,2,3,4a,5,6,6a,12b-octahydro-pyrano[3,2-a]xanthen-8,11-dion|(4aR)-9-((1S)-2cF-acetoxy-1rF,3tF-dimethyl-pent-catF-yl)-3t-(alpha-hydroxy-isopropyl)-6a,12b-dimethyl-(4ar,6at,12bt)-1,2,3,4a,5,6,6a,12b-octahydro-pyrano[3,2-a]xanthene-8,11-dione|anhydroisocochlioquinone A
16-Ac-30(8鈥樏傗垎9)-Abeo-3,11,16-trihydroxyfusida-7,17(20),24-trien-21-oic acid
12alpha-(3R-hydroxypentanoyloxy)-20,24-dimethyl-24-oxoscalara-16-en-25-al
3,4-secocycloarta-4(28),16,24-(Z)-triene-7beta,15alpha,20beta-trihydroxy-3-oic acid|angustific acid B
(24S)-16,24-anhydro-16,24,25-trihydroxy-2beta-methoxy-3,11,22-trioxocucurbit-5-ene
22-Ac-(3beta,22beta)-3,22-Dihydroxy-12-oleanen-30-oic acid
Ganoderic acid LM2
Lys Val Ile Arg
C23H46N8O5 (514.3590985999999)
Ganoderenic acid B
Ganoderenic acid B is a triterpenoid. CID 78074039 is a natural product found in Ganoderma applanatum and Ganoderma lucidum with data available. Ganoderenic acid B is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderenic acid B exhibits potent reversal effect on ABCB1-mediated multidrug resistance of HepG2/ADM cells to Doxorubicin[1].
Ganoderenic acid A
Ganoderenic acid A is a triterpenoid. (E)-6-[(7S,10S,13R,14R,15S,17R)-7,15-dihydroxy-4,4,10,13,14-pentamethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxohept-5-enoic acid is a natural product found in Ganoderma applanatum and Ganoderma lucidum with data available. Ganoderenic acid A is a lanostane-type triterpene. Ganoderenic acid A is a potent inhibitor of β-glucuronidase. Ganoderenic acid A has a potent hepatoprotective effect against CCl4-induced liver injury[1]. Ganoderenic acid A is a lanostane-type triterpene. Ganoderenic acid A is a potent inhibitor of β-glucuronidase. Ganoderenic acid A has a potent hepatoprotective effect against CCl4-induced liver injury[1].
Ganoderic acid J
C27H46O9_9,12,15-Octadecatrienoic acid, 3-(hexopyranosyloxy)-2-hydroxypropyl ester, (9Z,12Z,15Z)
C32H50O5_(3alpha,5xi,9xi,18xi)-3-Acetoxy-11-hydroxyurs-12-en-24-oic acid
Ala Ile Arg Arg
Ala Leu Arg Arg
Ala Arg Ile Arg
Ala Arg Leu Arg
Ala Arg Arg Ile
Ala Arg Arg Leu
Asp Lys Pro Arg
Asp Lys Arg Pro
Asp Pro Lys Arg
Asp Pro Arg Lys
Asp Arg Lys Pro
Asp Arg Pro Lys
Phe His Ile Val
C26H38N6O5 (514.2903537999999)
Phe His Leu Val
C26H38N6O5 (514.2903537999999)
Phe His Val Ile
C26H38N6O5 (514.2903537999999)
Phe His Val Leu
C26H38N6O5 (514.2903537999999)
Phe Ile His Val
C26H38N6O5 (514.2903537999999)
Phe Ile Val His
C26H38N6O5 (514.2903537999999)
Phe Leu His Val
C26H38N6O5 (514.2903537999999)
Phe Leu Val His
C26H38N6O5 (514.2903537999999)
Phe Val His Ile
C26H38N6O5 (514.2903537999999)
Phe Val His Leu
C26H38N6O5 (514.2903537999999)
Phe Val Ile His
C26H38N6O5 (514.2903537999999)
Phe Val Leu His
C26H38N6O5 (514.2903537999999)
His Phe Ile Val
C26H38N6O5 (514.2903537999999)
His Phe Leu Val
C26H38N6O5 (514.2903537999999)
His Phe Val Ile
C26H38N6O5 (514.2903537999999)
His Phe Val Leu
C26H38N6O5 (514.2903537999999)
His Ile Phe Val
C26H38N6O5 (514.2903537999999)
His Ile Val Phe
C26H38N6O5 (514.2903537999999)
His Leu Phe Val
C26H38N6O5 (514.2903537999999)
His Leu Val Phe
C26H38N6O5 (514.2903537999999)
His Val Phe Ile
C26H38N6O5 (514.2903537999999)
His Val Phe Leu
C26H38N6O5 (514.2903537999999)
His Val Ile Phe
C26H38N6O5 (514.2903537999999)
His Val Leu Phe
C26H38N6O5 (514.2903537999999)
Ile Ala Arg Arg
Ile Phe His Val
C26H38N6O5 (514.2903537999999)
Ile Phe Val His
C26H38N6O5 (514.2903537999999)
Ile His Phe Val
C26H38N6O5 (514.2903537999999)
Ile His Val Phe
C26H38N6O5 (514.2903537999999)
Ile Ile Asn Arg
Ile Ile Arg Asn
Ile Lys Arg Val
C23H46N8O5 (514.3590985999999)
Ile Lys Val Arg
C23H46N8O5 (514.3590985999999)
Ile Leu Asn Arg
Ile Leu Arg Asn
Ile Asn Ile Arg
Ile Asn Leu Arg
Ile Asn Arg Ile
Ile Asn Arg Leu
Ile Gln Arg Val
Ile Gln Val Arg
Ile Arg Ala Arg
Ile Arg Ile Asn
Ile Arg Lys Val
C23H46N8O5 (514.3590985999999)
Ile Arg Leu Asn
Ile Arg Asn Ile
Ile Arg Asn Leu
Ile Arg Gln Val
Ile Arg Arg Ala
Ile Arg Val Lys
C23H46N8O5 (514.3590985999999)
Ile Arg Val Gln
Ile Val Phe His
C26H38N6O5 (514.2903537999999)
Ile Val His Phe
C26H38N6O5 (514.2903537999999)
Ile Val Lys Arg
C23H46N8O5 (514.3590985999999)
Ile Val Gln Arg
Ile Val Arg Lys
C23H46N8O5 (514.3590985999999)
Ile Val Arg Gln
Lys Asp Pro Arg
Lys Asp Arg Pro
Lys Ile Arg Val
C23H46N8O5 (514.3590985999999)
Lys Ile Val Arg
C23H46N8O5 (514.3590985999999)
Lys Leu Arg Val
C23H46N8O5 (514.3590985999999)
Lys Leu Val Arg
C23H46N8O5 (514.3590985999999)
Lys Pro Asp Arg
Lys Pro Arg Asp
Lys Arg Asp Pro
Lys Arg Ile Val
C23H46N8O5 (514.3590985999999)
Lys Arg Leu Val
C23H46N8O5 (514.3590985999999)
Lys Arg Pro Asp
Lys Arg Val Ile
C23H46N8O5 (514.3590985999999)
Lys Arg Val Leu
C23H46N8O5 (514.3590985999999)
Lys Val Leu Arg
C23H46N8O5 (514.3590985999999)
Lys Val Arg Ile
C23H46N8O5 (514.3590985999999)
Lys Val Arg Leu
C23H46N8O5 (514.3590985999999)
Leu Ala Arg Arg
Leu Phe His Val
C26H38N6O5 (514.2903537999999)
Leu Phe Val His
C26H38N6O5 (514.2903537999999)
Leu His Phe Val
C26H38N6O5 (514.2903537999999)
Leu His Val Phe
C26H38N6O5 (514.2903537999999)
Leu Ile Asn Arg
Leu Ile Arg Asn
Leu Lys Arg Val
C23H46N8O5 (514.3590985999999)
Leu Lys Val Arg
C23H46N8O5 (514.3590985999999)
Leu Leu Asn Arg
Leu Leu Arg Asn
Leu Asn Ile Arg
Leu Asn Leu Arg
Leu Asn Arg Ile
Leu Asn Arg Leu
Leu Gln Arg Val
Leu Gln Val Arg
Leu Arg Ala Arg
Leu Arg Ile Asn
Leu Arg Lys Val
C23H46N8O5 (514.3590985999999)
Leu Arg Leu Asn
Leu Arg Asn Ile
Leu Arg Asn Leu
Leu Arg Gln Val
Leu Arg Arg Ala
Leu Arg Val Lys
C23H46N8O5 (514.3590985999999)
Leu Arg Val Gln
Leu Val Phe His
C26H38N6O5 (514.2903537999999)
Leu Val His Phe
C26H38N6O5 (514.2903537999999)
Leu Val Lys Arg
C23H46N8O5 (514.3590985999999)
Leu Val Gln Arg
Leu Val Arg Lys
C23H46N8O5 (514.3590985999999)
Leu Val Arg Gln
Asn Ile Ile Arg
Asn Ile Leu Arg
Asn Ile Arg Ile
Asn Ile Arg Leu
Asn Leu Ile Arg
Asn Leu Leu Arg
Asn Leu Arg Ile
Asn Leu Arg Leu
Asn Arg Ile Ile
Asn Arg Ile Leu
Asn Arg Leu Ile
Asn Arg Leu Leu
Pro Asp Lys Arg
Pro Asp Arg Lys
Pro Lys Asp Arg
Pro Lys Arg Asp
Pro Arg Asp Lys
Pro Arg Lys Asp
Pro Arg Arg Ser
C20H38N10O6 (514.2975647999999)
Pro Arg Ser Arg
C20H38N10O6 (514.2975647999999)
Pro Ser Arg Arg
C20H38N10O6 (514.2975647999999)
Gln Ile Arg Val
Gln Ile Val Arg
Gln Leu Arg Val
Gln Leu Val Arg
Gln Arg Ile Val
Gln Arg Leu Val
Gln Arg Val Ile
Gln Arg Val Leu
Gln Val Ile Arg
Gln Val Leu Arg
Gln Val Arg Ile
Gln Val Arg Leu
Arg Ala Ile Arg
Arg Ala Leu Arg
Arg Ala Arg Ile
Arg Ala Arg Leu
Arg Asp Lys Pro
Arg Asp Pro Lys
Arg Ile Ala Arg
Arg Ile Ile Asn
Arg Ile Lys Val
C23H46N8O5 (514.3590985999999)
Arg Ile Leu Asn
Arg Ile Asn Ile
Arg Ile Asn Leu
Arg Ile Gln Val
Arg Ile Arg Ala
Arg Ile Val Lys
C23H46N8O5 (514.3590985999999)
Arg Ile Val Gln
Arg Lys Ile Val
C23H46N8O5 (514.3590985999999)
Arg Lys Leu Val
C23H46N8O5 (514.3590985999999)
Arg Lys Val Ile
C23H46N8O5 (514.3590985999999)
Arg Lys Val Leu
C23H46N8O5 (514.3590985999999)
Arg Leu Ala Arg
Arg Leu Ile Asn
Arg Leu Lys Val
C23H46N8O5 (514.3590985999999)
Arg Leu Leu Asn
Arg Leu Asn Ile
Arg Leu Asn Leu
Arg Leu Gln Val
Arg Leu Arg Ala
Arg Leu Val Lys
C23H46N8O5 (514.3590985999999)
Arg Leu Val Gln
Arg Asn Ile Ile
Arg Asn Ile Leu
Arg Asn Leu Ile
Arg Asn Leu Leu
Arg Pro Arg Ser
C20H38N10O6 (514.2975647999999)
Arg Pro Ser Arg
C20H38N10O6 (514.2975647999999)
Arg Gln Ile Val
Arg Gln Leu Val
Arg Gln Val Ile
Arg Gln Val Leu
Arg Arg Ala Ile
Arg Arg Ala Leu
Arg Arg Ile Ala
Arg Arg Leu Ala
Arg Arg Pro Ser
C20H38N10O6 (514.2975647999999)
Arg Arg Ser Pro
C20H38N10O6 (514.2975647999999)
Arg Ser Pro Arg
C20H38N10O6 (514.2975647999999)
Arg Ser Arg Pro
C20H38N10O6 (514.2975647999999)
Arg Val Ile Lys
C23H46N8O5 (514.3590985999999)
Arg Val Ile Gln
Arg Val Lys Ile
C23H46N8O5 (514.3590985999999)
Arg Val Lys Leu
C23H46N8O5 (514.3590985999999)
Arg Val Leu Lys
C23H46N8O5 (514.3590985999999)
Arg Val Leu Gln
Arg Val Gln Ile
Arg Val Gln Leu
Ser Pro Arg Arg
C20H38N10O6 (514.2975647999999)
Ser Arg Pro Arg
C20H38N10O6 (514.2975647999999)
Ser Arg Arg Pro
C20H38N10O6 (514.2975647999999)
Val Phe His Ile
C26H38N6O5 (514.2903537999999)
Val Phe His Leu
C26H38N6O5 (514.2903537999999)
Val Phe Ile His
C26H38N6O5 (514.2903537999999)
Val Phe Leu His
C26H38N6O5 (514.2903537999999)
Val His Phe Ile
C26H38N6O5 (514.2903537999999)
Val His Phe Leu
C26H38N6O5 (514.2903537999999)
Val His Ile Phe
C26H38N6O5 (514.2903537999999)
Val His Leu Phe
C26H38N6O5 (514.2903537999999)
Val Ile Phe His
C26H38N6O5 (514.2903537999999)
Val Ile His Phe
C26H38N6O5 (514.2903537999999)
Val Ile Lys Arg
C23H46N8O5 (514.3590985999999)
Val Ile Gln Arg
Val Ile Arg Lys
C23H46N8O5 (514.3590985999999)
Val Ile Arg Gln
Val Lys Ile Arg
C23H46N8O5 (514.3590985999999)
Val Lys Leu Arg
C23H46N8O5 (514.3590985999999)
Val Lys Arg Ile
C23H46N8O5 (514.3590985999999)
Val Lys Arg Leu
C23H46N8O5 (514.3590985999999)
Val Leu Phe His
C26H38N6O5 (514.2903537999999)
Val Leu His Phe
C26H38N6O5 (514.2903537999999)
Val Leu Lys Arg
C23H46N8O5 (514.3590985999999)
Val Leu Gln Arg
Val Leu Arg Lys
C23H46N8O5 (514.3590985999999)
Val Leu Arg Gln
Val Gln Ile Arg
Val Gln Leu Arg
Val Gln Arg Ile
Val Gln Arg Leu
Val Arg Ile Lys
C23H46N8O5 (514.3590985999999)
Val Arg Ile Gln
Val Arg Lys Ile
C23H46N8O5 (514.3590985999999)
Val Arg Lys Leu
C23H46N8O5 (514.3590985999999)
Val Arg Leu Lys
C23H46N8O5 (514.3590985999999)
Val Arg Leu Gln
Val Arg Gln Ile
Val Arg Gln Leu
16-Acetylpriverogenin A
Oleanderolide 3-acetate
Tsugaric acid C
Ganoderic acid C
Ganoderic acid Z
Ganosporelactone B
Flavidulol C
Ganoderic acid V1
tert-butyl 1,6-diazaspiro[3.4]octane-1-carboxylate hemioxalate
17-[(E)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione
(2Z)-2-[(3R,4S,8S,9R,10S,13R,14R,16S)-3-hydroxy-4,10,14-trimethyl-11-oxo-16-propanoyloxy-2,3,4,5,6,7,8,9,12,13,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoic acid
3-(4-tert-butylphenyl)-1-[[(8R,9R)-6-[(2S)-1-hydroxypropan-2-yl]-8-methyl-5-oxo-10-oxa-1,6,13,14-tetrazabicyclo[10.2.1]pentadeca-12(15),13-dien-9-yl]methyl]-1-methylurea
2-(dimethylamino)-N-[(4R,7R,8S)-5-[(2-fluorophenyl)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]acetamide
C28H39FN4O4 (514.2955185999999)
3-(4-tert-butylphenyl)-1-[[(8R,9S)-6-[(2S)-1-hydroxypropan-2-yl]-8-methyl-5-oxo-10-oxa-1,6,13,14-tetrazabicyclo[10.2.1]pentadeca-12(15),13-dien-9-yl]methyl]-1-methylurea
3-(4-tert-butylphenyl)-1-[[(8R,9S)-6-[(2R)-1-hydroxypropan-2-yl]-8-methyl-5-oxo-10-oxa-1,6,13,14-tetrazabicyclo[10.2.1]pentadeca-12(15),13-dien-9-yl]methyl]-1-methylurea
3-(4-tert-butylphenyl)-1-[[(8S,9R)-6-[(2S)-1-hydroxypropan-2-yl]-8-methyl-5-oxo-10-oxa-1,6,13,14-tetrazabicyclo[10.2.1]pentadeca-12(15),13-dien-9-yl]methyl]-1-methylurea
3-cyclohexyl-1-[[(2R,3S)-8-(3-hydroxyhex-1-ynyl)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-1-methylurea
3-(4-tert-butylphenyl)-1-[[(8S,9R)-6-[(2R)-1-hydroxypropan-2-yl]-8-methyl-5-oxo-10-oxa-1,6,13,14-tetrazabicyclo[10.2.1]pentadeca-12(15),13-dien-9-yl]methyl]-1-methylurea
(Z)-6-[(3S,5R,7S,10S,13R,14R,17R)-3,7-dihydroxy-4,4,10,13,14-pentamethyl-11,15-dioxo-2,3,5,6,7,12,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxohept-5-enoic acid
(8S,9R,13R,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione
[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (9E,12E,15E)-octadeca-9,12,15-trienoate
(2-hydroxy-3-phosphonooxypropyl) (12Z,15Z,18Z,21Z)-tetracosa-12,15,18,21-tetraenoate
(1-heptanoyloxy-3-hydroxypropan-2-yl) (4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoate
[3-hydroxy-2-[(E)-tridec-8-enoyl]oxypropyl] (5E,7E,9E,11E,13E)-hexadeca-5,7,9,11,13-pentaenoate
2-[hydroxy-[2-hydroxy-3-[(3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoyl]oxypropoxy]phosphoryl]oxyethyl-trimethylazanium
eurysterol A sulfonic acid
A steroid sulfate that is 5alpha-cholestane substituted by hydroxy groups at positions 5 and 6, a bridged oxolane at positions 8 and 19 pand a sulfate group at position 3.
LPEt(22:4)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved