Exact Mass: 505.202
Exact Mass Matches: 505.202
Found 164 metabolites which its exact mass value is equals to given mass value 505.202
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
alangiside
An organic heterotetracyclic compound that is an alkaloidal glycoside isolated from Alangium salviifolium.
Rocaglamide
Rocaglamide is an organic heterotricyclic compound that is 2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]furan substituted by hydroxy groups at positions 1 and 8b, methoxy groups at positions 6 and 8, a 4-methoxyphenyl group at position 3a, a phenyl group at position 3 and a N,N-dimethylcarbamoyl group at position 1. Isolated from Aglaia odorata and Aglaia duperreana, it exhibits antineoplastic activity. It has a role as a metabolite, an antineoplastic agent and an antileishmanial agent. It is an organic heterotricyclic compound, a monomethoxybenzene and a monocarboxylic acid amide. Rocaglamide, also referred to as rocaglamide-A, is the eponymous member of a class of anti-cancer phytochemicals known as rocaglamides. Rocaglamides are secondary metabolites of the plant genus Aglaia, and extracts of the plant have traditionally been used as a form of insect repellant due to its natural insecticidal properties. Reports of Aglaia anti-tumor activity date back as far as 1973, and rocaglamide-A was first isolated in 1982 from the species A. elliptifolia. Rocaglamide and a number of its derivatives (e.g. [didesmethylrocaglamide]) are currently being studied for use as chemotherapeutic agents in the treatment of various leukemias, lymphomas, and carcinomas, as well as adjuvant therapy in the treatment of certain chemotherapy-resistant cancers. Rocaglamide is a natural product found in Aglaia rimosa, Aglaia elliptifolia, and other organisms with data available. An organic heterotricyclic compound that is 2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]furan substituted by hydroxy groups at positions 1 and 8b, methoxy groups at positions 6 and 8, a 4-methoxyphenyl group at position 3a, a phenyl group at position 3 and a N,N-dimethylcarbamoyl group at position 1. Isolated from Aglaia odorata and Aglaia duperreana, it exhibits antineoplastic activity.
Cys Asn Asn Arg
Cys Asn Arg Asn
Cys Pro Thr Trp
Cys Pro Trp Thr
Cys Gln Gln Gln
Cys Arg Asn Asn
Cys Thr Pro Trp
Cys Thr Trp Pro
Cys Trp Pro Thr
Cys Trp Thr Pro
Asp Asp Glu Lys
Asp Asp Lys Glu
Asp Glu Asp Lys
Asp Glu Lys Asp
Asp Lys Asp Glu
Asp Lys Glu Asp
Glu Asp Asp Lys
Glu Asp Lys Asp
Glu Glu Gln Thr
Glu Glu Thr Gln
Glu Lys Asp Asp
Glu Gln Glu Thr
Glu Gln Thr Glu
Glu Thr Glu Gln
Glu Thr Gln Glu
Lys Asp Asp Glu
Lys Asp Glu Asp
Lys Glu Asp Asp
Met Met Pro Gln
Met Met Gln Pro
Met Asn Asn Gln
Met Asn Gln Asn
Met Pro Met Gln
Met Pro Gln Met
Met Gln Met Pro
Met Gln Asn Asn
Met Gln Pro Met
Asn Cys Asn Arg
Asn Cys Arg Asn
Asn Met Asn Gln
Asn Met Gln Asn
Asn Asn Cys Arg
Asn Asn Met Gln
Asn Asn Gln Met
Asn Asn Arg Cys
Asn Gln Met Asn
Asn Gln Asn Met
Asn Arg Cys Asn
Asn Arg Asn Cys
Pro Cys Thr Trp
Pro Cys Trp Thr
Pro Met Met Gln
Pro Met Gln Met
Pro Gln Met Met
Pro Thr Cys Trp
Pro Thr Trp Cys
Pro Trp Cys Thr
Pro Trp Thr Cys
Gln Cys Gln Gln
Gln Glu Glu Thr
Gln Glu Thr Glu
Gln Met Met Pro
Gln Met Asn Asn
Gln Met Pro Met
Gln Asn Met Asn
Gln Asn Asn Met
Gln Pro Met Met
Gln Gln Cys Gln
Gln Gln Gln Cys
Gln Thr Glu Glu
Arg Cys Asn Asn
Arg Asn Cys Asn
Arg Asn Asn Cys
Thr Cys Pro Trp
Thr Cys Trp Pro
Thr Glu Glu Gln
Thr Glu Gln Glu
Thr Pro Cys Trp
Thr Pro Trp Cys
Thr Gln Glu Glu
Thr Trp Cys Pro
Thr Trp Pro Cys
Trp Cys Pro Thr
Trp Cys Thr Pro
Trp Pro Cys Thr
Trp Pro Thr Cys
Trp Thr Cys Pro
Trp Thr Pro Cys
TERT-BUTYL ((S)-1-((S)-2-CARBAMOYLPYRROLIDIN-1-YL)-1-OXO-3-(1-TOSYL-1H-IMIDAZOL-4-YL)PROPAN-2-YL)CARBAMATE
7-[(3S,5S)-3-amino-5-methylpiperidin-1-yl]-1-cyclopropyl-8-methoxy-4-oxoquinoline-3-carboxylic acid,2-hydroxybutanedioic acid
Nefazodone hydrochloride
D018377 - Neurotransmitter Agents > D014179 - Neurotransmitter Uptake Inhibitors > D000068760 - Serotonin and Noradrenaline Reuptake Inhibitors D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent D049990 - Membrane Transport Modulators Nefazodone hydrochloride (BMY-13754) is a potent and selective 5HT2A (Ki=5.8 nM) antagonist with moderate inhibition of 5-HT and noradrenaline uptake (IC50 of 290 and 300 nM, respectively). Nefazodone hydrochloride is a phenylpiperazine antidepressant with less alpha-adrenergic blocking activity[1][2].
Adavivint
C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor D000893 - Anti-Inflammatory Agents