Exact Mass: 260.181
Exact Mass Matches: 260.181
Found 180 metabolites which its exact mass value is equals to given mass value 260.181
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Falcarindiol
Constituent of roots of several plants including the common carrot (Daucus carota) and Angelica acutiloba (Dong Dang Gui). Falcarindiol is found in many foods, some of which are wild carrot, carrot, garden tomato (variety), and caraway. Falcarindiol is found in caraway. Falcarindiol is a constituent of roots of several plants including the common carrot (Daucus carota) and Angelica acutiloba (Dong Dang Gui). Falcarindiol is a natural product found in Anthriscus nitida, Chaerophyllum aureum, and other organisms with data available. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Carisoprodol
A centrally acting skeletal muscle relaxant whose mechanism of action is not completely understood but may be related to its sedative actions. It is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1202) M - Musculo-skeletal system > M03 - Muscle relaxants > M03B - Muscle relaxants, centrally acting agents > M03BA - Carbamic acid esters D018373 - Peripheral Nervous System Agents > D009465 - Neuromuscular Agents C78281 - Agent Affecting Musculoskeletal System > C29696 - Muscle Relaxant D002491 - Central Nervous System Agents
Ropinirole
Ropinirole is a non-ergoline dopamine agonist, manufactured by GlaxoSmithKline. It is used in the treatment of Parkinsons disease, and is also one of two medications in the United States with an FDA-approved indication for the treatment of restless legs syndrome (the other being Pramipexole). [Wikipedia] D002491 - Central Nervous System Agents > D018726 - Anti-Dyskinesia Agents > D000978 - Antiparkinson Agents N - Nervous system > N04 - Anti-parkinson drugs > N04B - Dopaminergic agents > N04BC - Dopamine agonists D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018491 - Dopamine Agonists C78272 - Agent Affecting Nervous System > C38149 - Antiparkinsonian Agent
Oxymetazoline
Oxymetazoline is only found in individuals that have used or taken this drug. It is a direct acting sympathomimetic used as a vasoconstrictor to relieve nasal congestion. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1251)Oxymetazoline is a direct acting sympathomimetic amine, which acts on alpha-adrenergic receptors in the arterioles of the conjunctiva and nasal mucosa. It produces vasoconstriction, resulting in decreased conjunctival congestion in ophthalmic. In nasal it produces constriction, resulting in decreased blood flow and decreased nasal congestion. R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AB - Sympathomimetics, combinations excl. corticosteroids R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AA - Sympathomimetics, plain S - Sensory organs > S01 - Ophthalmologicals > S01G - Decongestants and antiallergics > S01GA - Sympathomimetics used as decongestants D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013566 - Sympathomimetics C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D019141 - Respiratory System Agents > D014663 - Nasal Decongestants D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents D - Dermatologicals
2-Polyprenyl-6-methoxyphenol
This compound belongs to the family of Aromatic Monoterpenes. These are monoterpenes containing at least one aromatic ring
1,8-Heptadecadiene-4,6-diyne-3,10-diol
1,8-Heptadecadiene-4,6-diyne-3,10-diol is found in tea. 1,8-Heptadecadiene-4,6-diyne-3,10-diol is isolated from Panax quinquefolium (American ginseng). Isolated from Panax quinquefolium (American ginseng). 1,8-Heptadecadiene-4,6-diyne-3,10-diol is found in tea.
Panaxydol
Panaxydol is found in tea. Panaxydol is isolated from Panax ginseng (ginseng). Also from Panax quinquefolium (American ginseng). Isolated from Panax ginseng (ginseng)and is also from Panax quinquefolium (American ginseng). Panaxydol is found in tea.
1,9-Heptadecadiene-4,6-diyne-3,8-diol, (3S,8S,9Z)-
Falcarindiol
Falcarindiol is an organic molecular entity. It has a role as a metabolite. 1,9-Heptadecadiene-4,6-diyne-3,8-diol is a natural product found in Peucedanum oreoselinum, Oplopanax horridus, and other organisms with data available. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
(E)-17-Hydroxy-9-heptadecene-11,13-diyn-4-one|17-hydroxy-heptadec-9t-ene-11,13-diyn-4-one
(E)-2-(3,7-Dimethyl-2,6-octadienyl)-6-methyl-1,4-benzenediol
8-(hydroxymethyl)-4b,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol
(3beta)-podocarpa-8,11,13-triene-3,13-diol|isolophanthin C
9,10-cis-Epoxy-heptadec-16-ene-4,6-diyn-8-ol|cis-8,9-epoxy-heptadeca-1-en-11,13-diyn-10-ol
(2S,2?S,4?S)-4,5-diamino-2-hydroxypentanoic acid (1-carbamoyl-3-methylbutyl)amide
1beta,13-dihydroxy-8,11,13-podocarpatriene|1??,13-Dihydroxy-8,11,13-podocarpatriene
3alpha-hydroxypodocarpa-6,8(14)-dien-13-one|graciliflorin A
(3S,5aR,6S,8S,8aS)-3,6-dimethyl-8-(2-methylprop-1-en-1-yl)-3,4,5,5a,6,7,8,8aoctahydro-2H-naphtho[1,8-bc]furan-2-one|amphilectolide
1-methoxy-4-hydroxy-2-(3,7-dimethyl)-2E,6-octadienylbenzene
(9R,10S)-epoxyheptadecan-4,6-diyn-3-one|(9R,10S)-epoxyheptadecan-4,6-diyne-3-one
8S-heptadeca-2(Z)-9(Z)-diene-4,6-diine-1,8-diol|heptadeca-2c,9c-diene-4,6-diyne-1,8-diol|Heptadecadien-(2c,9c)-diin-(4,6)-diol-(1,8)
N-Demethyl-α-obscurine
carisoprodol
M - Musculo-skeletal system > M03 - Muscle relaxants > M03B - Muscle relaxants, centrally acting agents > M03BA - Carbamic acid esters D018373 - Peripheral Nervous System Agents > D009465 - Neuromuscular Agents C78281 - Agent Affecting Musculoskeletal System > C29696 - Muscle Relaxant D002491 - Central Nervous System Agents CONFIDENCE standard compound; EAWAG_UCHEM_ID 3327
[2-(carbamoyloxymethyl)-2-methylpentyl] N-propan-2-ylcarbamate
falcarindiol
(+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
ropinirole
D002491 - Central Nervous System Agents > D018726 - Anti-Dyskinesia Agents > D000978 - Antiparkinson Agents N - Nervous system > N04 - Anti-parkinson drugs > N04B - Dopaminergic agents > N04BC - Dopamine agonists D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018491 - Dopamine Agonists C78272 - Agent Affecting Nervous System > C38149 - Antiparkinsonian Agent CONFIDENCE standard compound; INTERNAL_ID 2711
(S)-2-[(TERT-BUTOXYCARBONYL)AMINO]-5-(DIMETHYLAMINO)PENTANOIC ACID
(R)-Methyl 5-(tert-butyldiMethylsilyloxy)-4-Methylpentanoate
(R)-3-Carboxy-2-(hexanoyloxy)-N,N,N-trimethylpropan-1-aminium
3-Carboxy-N,N,N-trimethyl-2-[(1-oxohexyl)oxy]-1-propanaminium
[3-Carboxy-2-(4-methylpentanoyloxy)propyl]-trimethylazanium
[3-Carboxy-2-(3-methylpentanoyloxy)propyl]-trimethylazanium
1-[4-(2,3-Dimethylphenyl)-1-piperazinyl]-2-methyl-1-propanone
[(2R)-3-carboxy-2-hexanoyloxypropyl]-dimethyl-(trideuteriomethyl)azanium
(2S,5R)-5-Methyl-2-(1-methyl-1-(4-methoxyphenyl)ethyl)-cyclohexanone
oxymetazoline
R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AB - Sympathomimetics, combinations excl. corticosteroids R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AA - Sympathomimetics, plain S - Sensory organs > S01 - Ophthalmologicals > S01G - Decongestants and antiallergics > S01GA - Sympathomimetics used as decongestants D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013566 - Sympathomimetics C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D019141 - Respiratory System Agents > D014663 - Nasal Decongestants D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents D - Dermatologicals
(8E,10E,12S)-heptadeca-8,10-dien-4,6-diyne-1,12-diol
2-[(2E)-3,7-dimethylocta-2,6-dienyl]-6-methoxyphenol
2-[(2z)-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-ylidene]acetaldehyde
2-(5,8-dimethyl-1,2,3,4-tetrahydronaphthalen-2-yl)propan-2-yl acetate
(4bs,5r,8as)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-2,5-diol
[1,2-dimethyl-2-(4-methylphenyl)cyclopentyl]methyl acetate
(5r)-3-[(1e)-dodec-1-en-11-yn-1-yl]-5-methyl-5h-furan-2-one
(3r)-8-[(2r,3r)-3-heptyloxiran-2-yl]oct-1-en-4,6-diyn-3-ol
[(1s,2s)-1,2-dimethyl-2-(4-methylphenyl)cyclopentyl]methyl acetate
(2s,4as,10ar)-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,7-diol
(1s,9r,10s,16s)-16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-5-ol
(3s,8e,10r)-heptadeca-1,8-dien-4,6-diyne-3,10-diol
2-(3,7-dimethylocta-2,6-dien-1-yl)-5-(hydroxymethyl)phenol
[4-(1,2-dimethyl-3-methylidenecyclopentyl)cyclohexa-1,4-dien-1-yl]methyl acetate
1β,13-dihydroxy-8,11,13-podocarpatriene
{"Ingredient_id": "HBIN002338","Ingredient_name": "1\u03b2,13-dihydroxy-8,11,13-podocarpatriene","Alias": "NA","Ingredient_formula": "C17H24O2","Ingredient_Smile": "CC1(CCC(C2(C1CCC3=C2C=CC(=C3)O)C)O)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "6098","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
8-(e)-heptadeca-1,8-dien-4,6-diyn-3,10-diol
{"Ingredient_id": "HBIN013710","Ingredient_name": "8-(e)-heptadeca-1,8-dien-4,6-diyn-3,10-diol","Alias": "NA","Ingredient_formula": "C17H24O2","Ingredient_Smile": "CCCCCCCC(C=CC#CC#CC(C=C)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "31076","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
9,10-epoxy-16-heptadecene-4,6-diyn-8-ol
{"Ingredient_id": "HBIN013952","Ingredient_name": "9,10-epoxy-16-heptadecene-4,6-diyn-8-ol","Alias": "NA","Ingredient_formula": "C17H24O2","Ingredient_Smile": "NA","Ingredient_weight": "260.37","OB_score": "NA","CAS_id": "73566-32-2","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "7298","PubChem_id": "NA","DrugBank_id": "NA"}
(9r,10s)-epoxyheptadecan-4,6-diyn-3-one
{"Ingredient_id": "HBIN014180","Ingredient_name": "(9r,10s)-epoxyheptadecan-4,6-diyn-3-one","Alias": "NA","Ingredient_formula": "C17H24O2","Ingredient_Smile": "CCCCCCCCCCC#CC#CC(=O)CC=O","Ingredient_weight": "260.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT15285","TCMID_id": "7103","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "129716080","DrugBank_id": "NA"}