Exact Mass: 484.1846

Exact Mass Matches: 484.1846

Found 269 metabolites which its exact mass value is equals to given mass value 484.1846, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Nb-trans-p-Coumaroylserotonin glucoside

(2E)-3-(4-Hydroxyphenyl)-N-[2-(5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H-indol-3-yl)ethyl]prop-2-enimidate

C25H28N2O8 (484.1846)

Nb-trans-p-Coumaroylserotonin glucoside is found in fats and oils. It is an alkaloid from Carthamus tinctorius (safflower) If neurons that make serotonin serotonergic neurons are abnormal in infants, there is a risk of sudden infant death syndrome (SIDS). Low levels of serotonin may also be associated with intense spiritual experiences. In animals including humans, serotonin is synthesized from the amino acid L-tryptophan by a short metabolic pathway consisting of two enzymes: tryptophan hydroxylase (TPH) and amino acid decarboxylase (DDC). The TPH-mediated reaction is the rate-limiting step in the pathway. TPH has been shown to exist in two forms: TPH1, found in several tissues, and TPH2, which is a brain-specific isoform. There is evidence that genetic polymorphisms in both these subtypes influence susceptibility to anxiety and depression in humans.[citation needed] The 5-HTT gene regulates a chemical called serotonin. This chemical is found in very low amounts in people diagnosed with depression compared to other people. Serotonin works as a neurotransmitter and helps with the modulation of things such as anger, appetite, sexuality, sleep, mood, and several other things. People with depression often have impaired 5-HTT genes. There are two forms of the 5-HTT gene and everyone has two 5-HTT genes. (Levinson) There is a long form of 5-HTT and a short form of 5-HTT. Research shows that people with both 5-HTT genes being the long form are less likely to become depressed while people with one short and one long or two short forms are more likely to develop depression. Research is still being conducted to find more information. There is also evidence that ovarian hormones can affect the expression of TPH in various species, suggesting a possible mechanism for postpartum depression and premenstrual stress syndrome.[citation needed] Serotonin biosynthesis in plants likewise begins with L-tryptophan, which is however first decarboxylated by tryptophan decarboxylase to give tryptamine, which is then hydroxylated by the cytochrome P450 monooxygenase, tryptamine 5-hydroxylase, yielding serotonin. Serotonin is a biochemical messenger and regulator, synthesized from the essential amino acid L-Tryptophan. Serotonin in the nervous system acts as a local transmitter at synapses, and as a paracrine or hormonal modulator of circuits upon diffusion, allowing a wide variety of "state-dependent" behavioral responses to different stimuli. Serotonin is widely distributed in the nervous system of vertebrates and invertebrates and some of its behavioral effects have been preserved along evolution. Such is the case of aggressive behavior and rhythmic motor patterns , including those responsible for feeding. In vertebrates, which display a wider and much more sophisticated behavioral repertoire, serotonin also modulates sleep , the arousal state , sexual behavior, and others, and deficiencies of the serotonergic system causes disorders such as depression, obsessive-compulsive disorder, phobias, posttraumatic stress disorder, epilepsy, and generalized anxiety disorder. Serotonin has three different modes of action in the nervous system: as transmitter, acting locally at synaptic boutons; Serotonin is a monoamine neurotransmitter. It is found extensively in the gastrointestinal tract of animals, and about 80 to 90 percent of the human bodys total serotonin is located in the enterochromaffin cells in the gut, where it is used to regulate intestinal movements. The remainder is synthesized in serotonergic neurons in the central nervous system (CNS) where it has various functions, including the regulation of mood, appetite, sleep, muscle contraction, and some cognitive functions including memory and learning. Serotonin levels can not be increased by diet alone. For example, increasing foods rich in tryptophan (e.g., meats, proteins) does not increase serotonin levels, due to competition with other amino acids. What is required to increase serotonin producti... Alkaloid from Carthamus tinctorius (safflower) [DFC]. Nb-trans-p-Coumaroylserotonin glucoside is found in fats and oils and herbs and spices.

Thamnosin

7-Methoxy-6-[2-[2-(7-methoxy-2-oxo-2H-1-benzopyran-6-yl)-1,4-dimethyl-3-cyclohexen-1-yl]ethenyl]-2H-1-benzopyran-2-one, 9ci

C30H28O6 (484.1886)

Thamnosin is found in citrus. Thamnosin is a constituent of Citrus grandis (pummelo)

Halobetasol Propionate

[(6S,9R,16S,17R)-17-(2-chloroacetyl)-6,9-difluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate

C25H31ClF2O5 (484.1828)

Halobetasol propionate is thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2. It is used for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

managlinat dialanetil

ethyl 2-[({5-[2-amino-5-(2-methylpropyl)-1,3-thiazol-4-yl]furan-2-yl}[(1-ethoxy-1-oxopropan-2-yl)amino]phosphanyl)amino]propanoate

C21H33N4O5PS (484.1909)

Plantacyanin

9-{4-[4-(9H-carbazol-9-yl)phenyl]phenyl}-9H-carbazole

C36H24N2 (484.1939)

Isolated from cucumber. Plantacyanin is found in green vegetables.

diuvaretin

1- [ 2,4-Dihydroxy-3,5-bis [ (2-hydroxyphenyl) methyl ] -6-methoxyphenyl ] -3-phenyl-1-propanone

C30H28O6 (484.1886)

A member of the class of dihydrochalcones that is dihydrochalcone substituted by 2-hydroxybenzyl groups at positions 3 and 5, hydroxy groups at positions 2 and 4 and a methoxy group at position 6. Isolated from the roots of Uvaria acuminata and Uvaria chamae, it exhibits cytotoxicity towards human promyelocytic leukemia HL-60 cells.

2,7-dimethyl-1,4-dihydronaphthalene-5,8-diol 5-O-beta-D-xylopyranosyl(1->6)-beta-D-glucopyranoside|2,7-Dimethyl-1,4-dihydronaphthalene-5,8-diol 5-O-??-D-xylopyranosyl(1鈥樏傗垎6)-??-D-glucopyranoside

2,7-dimethyl-1,4-dihydronaphthalene-5,8-diol 5-O-beta-D-xylopyranosyl(1->6)-beta-D-glucopyranoside|2,7-Dimethyl-1,4-dihydronaphthalene-5,8-diol 5-O-??-D-xylopyranosyl(1鈥樏傗垎6)-??-D-glucopyranoside

C23H32O11 (484.1945)

Phebalin

C30H28O6 (484.1886)

(3R,5S,6S,9S,10S*)-3-bromo-6,12-diacetoxy-13-hydroxylabd-8(19),14-diene

(3R*,5S*,6S*,9S*,10S*)-3-bromo-6,12-diacetoxy-13-hydroxylabd-8(19),14-diene

C24H37BrO5 (484.1824)

C25H28N2O8

C25H28N2O8 (484.1846)

ovatic acid methyl ester 7-O-(6-O-p-hydroxybenzoyl)-beta-D-glucopyranoside|Ovatic acid methyl ester 7-O-(6-O-p-hydroxybenzoyl)-??-D-glucopyranoside

C23H32O11 (484.1945)

solenolide F

C24H33ClO8 (484.1864)

Shancilin

C30H28O6 (484.1886)

5-hydroxy-mappicine-20-O-beta-glucopyranoside

C25H28N2O8 (484.1846)

(1S,2S,3S,7R,8S,9R,11R,12S,14R*)-7-bromotetradecahydro-12-hydroxy-1-isopropyl-8,12-dimethyl-4-methylenephenanthren-9,14-yl diacetate

(1S*,2S*,3S*,7R*,8S*,9R*,11R*,12S*,14R*)-7-bromotetradecahydro-12-hydroxy-1-isopropyl-8,12-dimethyl-4-methylenephenanthren-9,14-yl diacetate

C24H37BrO5 (484.1824)

(12R)-6alpha,19-diacetoxy-18-chloro-1beta,12-epoxy-4alpha-hydroxy-neo-clerod-13-en-15,16-olide|ajugaciliatin F

C24H33ClO8 (484.1864)

17-hydroxymappicine 20-O-beta-D-glucopyranoside

C25H28N2O8 (484.1846)

Phochinenin I

C30H28O6 (484.1886)

cadinanolide|CPB-2001-49-1359-1

C23H32O11 (484.1945)

Phochinenin K

C30H28O6 (484.1886)

Phochinenin J

C30H28O6 (484.1886)

(+-)-3r-(7-Methoxy-2-oxo-2H-chromen-8-yl)-4c-[trans-2-(7-methoxy-2-oxo-2H-chromen-8-yl)-vinyl]-1,4t-dimethyl-cyclohexen|(+-)-3r-(7-methoxy-2-oxo-2H-chromen-8-yl)-4c-[trans-2-(7-methoxy-2-oxo-2H-chromen-8-yl)-vinyl]-1,4t-dimethyl-cyclohexene

(+-)-3r-(7-Methoxy-2-oxo-2H-chromen-8-yl)-4c-[trans-2-(7-methoxy-2-oxo-2H-chromen-8-yl)-vinyl]-1,4t-dimethyl-cyclohexen|(+-)-3r-(7-methoxy-2-oxo-2H-chromen-8-yl)-4c-[trans-2-(7-methoxy-2-oxo-2H-chromen-8-yl)-vinyl]-1,4t-dimethyl-cyclohexene

C30H28O6 (484.1886)

(+)-tephrorin B|(3S,4S)-4-[(2S)-3,4-dihydro-7-hydroxy-4-oxo-2-phenyl-2H-1-benzopyran-8-yl]tetrahydro-2,2-dimethyl-3-furanyl (2E)-3-phenyl-2-propenoate

C30H28O6 (484.1886)

7-[4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol

C30H28O6 (484.1886)

Ala Glu Glu His

(4S)-4-[(2S)-2-[(2S)-2-aminopropanamido]-4-carboxybutanamido]-4-{[(1S)-1-carboxy-2-(1H-imidazol-4-yl)ethyl]carbamoyl}butanoic acid

C19H28N6O9 (484.1918)

Ala Glu His Glu

(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-aminopropanamido]-4-carboxybutanamido]-3-(1H-imidazol-4-yl)propanamido]pentanedioic acid

C19H28N6O9 (484.1918)

Ala His Glu Glu

(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-aminopropanamido]-3-(1H-imidazol-4-yl)propanamido]-4-carboxybutanamido]pentanedioic acid

C19H28N6O9 (484.1918)

Cys Cys Phe Ile

(2S,3S)-2-[(2S)-2-[(2R)-2-[(2R)-2-amino-3-sulfanylpropanamido]-3-sulfanylpropanamido]-3-phenylpropanamido]-3-methylpentanoic acid