Exact Mass: 282.10226539999996
Exact Mass Matches: 282.10226539999996
Found 251 metabolites which its exact mass value is equals to given mass value 282.10226539999996,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Xylobiose
Xylobiose is a glycosylxylose that is D-xylopyranose having a beta-D-xylopyranosyl residue attached at position 4 via a glycosidic bond. It has a role as a bacterial metabolite. Xylobiose is a natural product found in Streptomyces ipomoeae, Chlamydomonas reinhardtii, and Streptomyces rameus with data available. 4-O-beta-D-Xylopyranosyl-L-arabinose is found in fruits. 4-O-beta-D-Xylopyranosyl-L-arabinose is isolated from acid hydrolysate of peach gum. Isolated from acid hydrolysate of peach gum. 4-O-beta-D-Xylopyranosyl-L-arabinose is found in fruits. Xylobiose (1,4-β-D-Xylobiose; 1,4-D-Xylobiose) is a disaccharide?of?xylose?monomers with a β-1, 4 bond between monomers[1].
2-Hydroxynevirapine
2-Hydroxynevirapine is only found in individuals that have used or taken Nevirapine. 2-Hydroxynevirapine is a metabolite of Nevirapine. 2-hydroxynevirapine belongs to the family of Pyridinones. These are compounds containing a pyridine ring, which bears a ketone.
2-Aminoadenosine
2-Aminoadenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1].
Dehydrocoformycin
A coformycin derivative in which the hydroxy group on the diazepine ring of coformycin is replaced by an oxo group.
beta-L-Arabinofuranosyl-(1->2)-beta-L-arabinofuranose
5-O-a-L-Arabinofuranosyl-L-arabinose
5-O-a-L-Arabinofuranosyl-L-arabinose is found in fruits. 5-O-a-L-Arabinofuranosyl-L-arabinose is from stem mucilage of Opuntia ficus-indica (Indian fig). It is isolated from partial acid hydrolysates of sugar beet araban. From stem mucilage of Opuntia ficus-indica (Indian fig). Isolated from partial acid hydrolysates of sugar beet araban. 5-O-a-L-Arabinofuranosyl-L-arabinose is found in fruits and root vegetables.
Arabinofuranobiose
Arabinofuranobiose is formed on partial acid hydrolysis of sugar beet araban and certain plant gums. Arabinofuranobiose belongs to the family of Other Disaccharides. These are disaccharides that are neither an hexose disaccharide nor a mixed hexose/pentose disaccharide.
5-O-beta-D-Xylopyranosyl-L-arabinose
5-O-beta-D-Xylopyranosyl-L-arabinose is found in fruits. 5-O-beta-D-Xylopyranosyl-L-arabinose is isolated from partial acid hydrolysates of peach, Cholla (Opuntia fulgida), Opuntia ficus-indica (Indian fig) and Virgilia oroboides gums. Isolated from partial acid hydrolysates of peach, Cholla (Opuntia fulgida), Opuntia ficus-indica (Indian fig) and Virgilia oroboides gums. 5-O-beta-D-Xylopyranosyl-L-arabinose is found in fruits.
Arabinopyranobiose
Arabinopyranobiose is found in citrus. Arabinopyranobiose is isolated from partial acid hydrolysates of golden apple (Spondias cytherea), lemon, peach, cherry. Also major disaccharide product from the acid reversion of L-arabinos
2-O-b-D-Xylopyranosyl-L-arabinose
2-O-b-D-Xylopyranosyl-L-arabinose is found in cereals and cereal products. 2-O-b-D-Xylopyranosyl-L-arabinose is isolated from barley husk and corn-cob hemicelluloses. Isolated from barley husk and corn-cob hemicelluloses. 2-O-b-D-Xylopyranosyl-L-arabinose is found in cereals and cereal products.
N1-methylinosine
1-methylinosine is inosine carrying a methyl substituent at position 1 on the hypoxanthine ring. It has a role as a metabolite. It derives from an inosine. It is a modified nucleotide found at position 37 in tRNA 3 to the anticodon of eukaryotic tRNA. Shown that sequences are forced to adopt a hairpin conformation if one of the central 6 nt is replaced by the corresponding methylated nucleotide, such as 1-methylguanosine. In Vivo synthesis: Inosine-37 in tRNA is synthesised by a hydrolytic deamination-type reaction, catalysed by distinct tRNA:adenosine deaminases. Modified nucleotide found at position 37 in tRNA 3 to the anticodon of eukaryotic tRNA. Shown that sequences are forced to adopt a hairpin conformation if one of the central 6 nt is replaced by the corresponding methylated nucleotide, such as 1-methylguanosine. 1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA[1]. 1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA[1].
12-Hydroxynevirapine
12-Hydroxynevirapine is only found in individuals that have used or taken Nevirapine. 12-Hydroxynevirapine is a metabolite of Nevirapine. 12-hydroxynevirapine belongs to the family of 1,4-Diazepines. These are organic compounds containing 1,4-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 4.
8-Hydroxynevirapine
8-Hydroxynevirapine is only found in individuals that have used or taken Nevirapine. 8-Hydroxynevirapine is a metabolite of Nevirapine. 8-hydroxynevirapine belongs to the family of 1,4-Diazepines. These are organic compounds containing 1,4-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 4.
3-Hydroxynevirapine
3-Hydroxynevirapine is only found in individuals that have used or taken Nevirapine. 3-Hydroxynevirapine is a metabolite of Nevirapine. 3-hydroxynevirapine belongs to the family of 1,4-Diazepines. These are organic compounds containing 1,4-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 4.
3-O-alpha-L-Arabinopyranosyl-L-arabinose
Hydrolysate product from the stem mucilage of Opuntia ficus-indica (Indian fig). 3-O-b-D-Xylopyranosyl-L-arabinose is found in fruits. 3-O-b-D-Xylopyranosyl-L-arabinose is found in fruits. Hydrolysate product from the stem mucilage of Opuntia ficus-indica (Indian fig).
3-(Hydroxymethyl)-5,5-diphenylimidazolidine-2,4-dione
C16H14N2O3 (282.10043740000003)
bendazac
C16H14N2O3 (282.10043740000003)
M - Musculo-skeletal system > M02 - Topical products for joint and muscular pain > M02A - Topical products for joint and muscular pain > M02AA - Antiinflammatory preparations, non-steroids for topical use S - Sensory organs > S01 - Ophthalmologicals > S01B - Antiinflammatory agents > S01BC - Antiinflammatory agents, non-steroids C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents
2-{2-[3-(2-Carbamimidoylsulfanyl-ethyl)-phenyl]-ethyl}-isothiourea
S,S'-(1,4-Phenylene-bis(1,2-ethanediyl))bis-isothiourea
3-O-alpha-D-Xylopyranosyl-L-arabinose
Isolated from the autohydrolysate of golden apple (Spondias cytherea), gum, garden cress mucilage and the partial acid hydrolysates of corn hemicelluloses. 3-O-alpha-D-Xylopyranosyl-L-arabinose is found in cereals and cereal products, fruits, and green vegetables.
Multiplolide B
A 10-membered lactone obtained from 10-methyl-9,10-dihydro-2H-oxecin-2-one by the epoxidation of the double bond at position 3-4 and cis-dihydroxylation of the double bond at position 7-8, with further acylation of the hydroxy group at position 8 by a but-2-enoyl group. Multiplolide B was first isolated from the fungus Xylaria multiplex BCC 1111. It shows antifungal activity against Candida albicans. The epoxide group has cis-configuration, but its configuration relative to the other substituents was not established.
(3R)-3-(beta-D-glucopyranosyloxy)-4-hydroxybutanoic acid
3-O-alpha-D-xylopyranosyl-L-arabinose|O3-alpha-D-Xylopyranosyl-L-arabinose
2,3-Dihydroxymethyl-4-(3,4-dimethoxyphenyl)-??-butyrolactone
5-O-alpha-L-Arabinofuranosyl-L-arabinose|O5-alpha-L-Arabinofuranosyl-arabinose
(6R,12R,14R)-(3E,9E)-12-hydroxy-6,14-dimethyl-1,7-dioxacyclotetradeca-3,9-diene-2,8,11-trione|11-Ketonee-Colletodiol|6R,12R,14R-colletoketol|colletoketol|grahamimycin A|Grahamimycin A1
5-hydroxymethyl-9-methoxycanthin-6-one
C16H14N2O3 (282.10043740000003)
(Z)-2-(4-hydroxyphenyl)ethenyl-alpha-L-rhamnopyranoside
2-deoxy-4-O-alpha-D-galactopyranosyl-D-glycero-tetronic acid
(3S*,4S*)-3,4-dihydro-3,4,8-trihydroxy-6-methoxy-7-(1-methoxyethyl)naphthalen-1(2H)-one|botryosphaerone C
6-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dioxabicyclo-[3.3.0]-octane
alpha-(3-Chloro-1-propenyl)-6-(2-penten-4-ynyl)-2,5-dioxabicyclo[2,2,1]heptane-3-ethanol
C15H19ClO3 (282.10226539999996)
(-)-grahamimycin A1|(R,R)-(-)-Grahamimycin A1|grahamimycin|Grahamimycin A1
3-O-alpha-D-galactopyranosyl-2-C-methylglyceric acid
(E)-4,5,6,7-tetrahydroxy-2-benzylhept-2-enoic acid|drypearmoracein A
1,4-Di Me ether,di-Ac-3,6-Dimethyl-1,2,4,5-benzenetetrol
(3R*,4R*)-3,4-dihydro-3,4,8-trihydroxy-3-(2-hydroxypropyl)-6-methoxynaphthalen-1(2H)-one|balticol E
Succinic acid 1-butyl 4-(5-formyl-2-furylmethyl) ester
Di-Me ether,Me ester-1,3-Dihydro-3,7-dihydroxy-5-methoxy-6-methyl-4-isobenzofurancarboxylic acid
Ellipticine
Ellipticine (NSC 71795) hydrochloride is a potent antineoplastic agent; inhibits DNA topoisomerase II activities. Ellipticine (NSC 71795) hydrochloride is a potent antineoplastic agent; inhibits DNA topoisomerase II activities.
Methyl 4,6-O-benzylidene-α-D-glucopyranoside
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.717 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.718
C11H14N4O5_6H-Purin-6-one, 1,9-dihydro-9-(3-O-methylpentofuranosyl)
C14H18O6_Heptonic acid, 4,7-anhydro-2-deoxy-7-C-phenyl-, methyl ester
2-O-Methylinosine
Inosine carrying a methyl substituent on the hydroxy group at position 2 on the ribose ring. 9-((2R,3R,4R,5R)-4-Hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-9H-purin-6-ol (2'-O-methylinosine) is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
methyl 3-(3,4-dihydroxy-5-phenyloxolan-2-yl)-3-hydroxypropanoate
Di(2-methoxyethyl) phthalate
CONFIDENCE standard compound; INTERNAL_ID 397; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7846; ORIGINAL_PRECURSOR_SCAN_NO 7843 CONFIDENCE standard compound; INTERNAL_ID 397; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7826; ORIGINAL_PRECURSOR_SCAN_NO 7822 CONFIDENCE standard compound; INTERNAL_ID 397; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7851; ORIGINAL_PRECURSOR_SCAN_NO 7849
methyl 3-(3,4-dihydroxy-5-phenyloxolan-2-yl)-3-hydroxypropanoate_0.5\\%
methyl 3-(3,4-dihydroxy-5-phenyloxolan-2-yl)-3-hydroxypropanoate_major
1-Methylinosine
Inosine carrying a methyl substituent at position 1 on the hypoxanthine ring. 1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA[1]. 1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA[1].
12-Hydroxynevirapine
A dipyridodiazepine that is nevirapine in which one of the hydrogens of the methyl group has been substituted by a hydroxy group. It is a metabolite of the anti-HIV drug, nevirapine.
2-Hydroxynevirapine
8-Hydroxynevirapine
3-Hydroxynevirapine
Arabinofuranobiose
4-Methyl-n3-(4-pyridin-3-yl-thiazol-2-yl)-benzene-1,3-diamine
bis(2,3-epoxypropyl) cyclohex-4-ene-1,2-dicarboxylate
METHYL 7-(BENZYLOXY)-1H-INDAZOLE-3-CARBOXYLATE
C16H14N2O3 (282.10043740000003)
Methyl 5-(benzyloxy)-1H-indazole-3-carboxylate
C16H14N2O3 (282.10043740000003)
(7R,9AR)-TERT-BUTYL7-(AMINOMETHYL)HEXAHYDRO-1H-PYRIDO[1,2-A]PYRAZINE-2(6H)-CARBOXYLATE
C16H14N2O3 (282.10043740000003)
Trimethylsilyl p-(trimethylsilyloxy)benzoate
7-(benzyloxy)-6-methoxyquinazolin-4-ol
C16H14N2O3 (282.10043740000003)
4-(4-METHYLPIPERAZIN-1-YL)-3-(METHYLSULFONYL)BENZALDEHYDE
2-[(2-CARBOMETHOXYPHENOXY)METHYL]-BENZIMIDAZOLE
C16H14N2O3 (282.10043740000003)
5(6)-carbethoxy-2-(4-hydroxyphenyl)-benzimidazole
C16H14N2O3 (282.10043740000003)
2-(4-AMino-2-ethoxyphenyl)pthaliMide
C16H14N2O3 (282.10043740000003)
3-(Methylsulfonyl)phenylboronic Acid Pinacol Ester
[4-[Bis(2-hydroxyethyl)amino]phenyl]-1,1,2-ethylenetricarbonitrile
4-(4-METHYLPIPERAZIN-1-YL)-2-(METHYLSULFONYL)BENZALDEHYDE
Methyl 6-(benzyloxy)-1H-indazole-3-carboxylate
C16H14N2O3 (282.10043740000003)
TRIMETHYLSILYL TRIMETHYLSILOXY SALICYLATE
a-D-Mannopyranoside, methyl4,6-O-(phenylmethylene)-
Ethyl 4-(1,3-benzoxazol-2-ylamino)benzoate
C16H14N2O3 (282.10043740000003)
(1-BENZYL-1H-IMIDAZOL-2-YL)METHANOL
C16H14N2O3 (282.10043740000003)
4,4,5,5-TETRAMETHYL-2-(4-(METHYLSULFONYL)PHENYL)-1,3,2-DIOXABOROLANE
Trilithium citrate tetrahydrate
C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent Lithium citrate (Litarex) tetrahydrate is the major active ingredient of Garcinia cambogia. Lithium citrate tetrahydrate competitively inhibits ATP citrate lyase with weight loss benefits. Lithium citrate tetrahydrate effective inhibits stones formation and also inhibits HIF, and has antioxidation, anti-inflammation and anti-tumor effects[1][2][3][4]. Lithium citrate (Litarex) tetrahydrate is the major active ingredient of Garcinia cambogia. Lithium citrate tetrahydrate competitively inhibits ATP citrate lyase with weight loss benefits. Lithium citrate tetrahydrate effective inhibits stones formation and also inhibits HIF, and has antioxidation, anti-inflammation and anti-tumor effects[1][2][3][4]. Lithium citrate (Litarex) tetrahydrate is the major active ingredient of Garcinia cambogia. Lithium citrate tetrahydrate competitively inhibits ATP citrate lyase with weight loss benefits. Lithium citrate tetrahydrate effective inhibits stones formation and also inhibits HIF, and has antioxidation, anti-inflammation and anti-tumor effects[1][2][3][4]. Lithium citrate (Litarex) tetrahydrate is the major active ingredient of Garcinia cambogia. Lithium citrate tetrahydrate competitively inhibits ATP citrate lyase with weight loss benefits. Lithium citrate tetrahydrate effective inhibits stones formation and also inhibits HIF, and has antioxidation, anti-inflammation and anti-tumor effects[1][2][3][4].
2-(3-FORMYL-INDOL-1-YL)-N-FURAN-2-YLMETHYL-ACETAMIDE
C16H14N2O3 (282.10043740000003)
(2-Methyl sulfonyl penyl)boronic acid pinacol ester
Methyl 4-(benzyloxy)pyrazolo[1,5-a]pyridine-3-carboxylate
C16H14N2O3 (282.10043740000003)
METHYL 1-(2-ETHOXYETHYL)-4,5,6,7-TETRAHYDRO-5,7-DIOXO-1H-PYRAZOLO[4,3-D]PYRIMIDINE-3-CARBOXYLATE
3-oxo-3-(2,3,4-trimethoxyphenyl)propionic acid ethyl ester
8-Aminoadenosine
8-Aminoadenosine (8-NH2-Ado), a RNA-directed nucleoside analogue, reduces cellular ATP levels and inhibits mRNA synthesis. 8-Aminoadenosine blocks Akt/mTOR signaling and induces autophagy and apoptosis in a p53-independent manner. 8-Aminoadenosine has antitumor activity[1][2][3]. 8-Aminoadenosine (8-NH2-Ado), a RNA-directed nucleoside analogue, reduces cellular ATP levels and inhibits mRNA synthesis. 8-Aminoadenosine blocks Akt/mTOR signaling and induces autophagy and apoptosis in a p53-independent manner. 8-Aminoadenosine has antitumor activity[1][2][3].
5-Amino-4-(4-cyclopropyl-1-naphthalenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
5-(4-methoxyphenyl)-5-phenylimidazolidine-2,4-dione
C16H14N2O3 (282.10043740000003)
1,3,4-Oxadiazole,2,5-bis(3-methoxyphenyl)-
C16H14N2O3 (282.10043740000003)
Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-3-carboxylate
2-(4-Methylpiperazin-1-yl)-4-(methylsulfonyl)benzaldehyde
ETHYL 6,6-DIMETHYL-3-HYDRAZINO-4-OXO-4,5,6,7-TETRAHYDROBENZO(C)THIOPHENE-1-CARBOXYLATE, TECH.
7-methoxy-6-phenylmethoxy-1H-quinazolin-4-one
C16H14N2O3 (282.10043740000003)
1-(3-Nitro-10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)ethanone
C16H14N2O3 (282.10043740000003)
1H-Pyrrolo[2,3-b]pyridine-5-carboxylicacid,1-[(4-Methoxyphenyl)Methyl]-
C16H14N2O3 (282.10043740000003)
1-ethyl-3-methylimidazol-3-ium,4-methylbenzenesulfonate
N-(4-methoxybenzyl)-3-(trifluoromethyl)pyridin-2-amine
4-Methyl-N3-[4-(3-pyridinyl)-1,3-thiazol-2-yl]-1,3-benzenediamine
METHYL 5-(BENZYLOXY)PYRAZOLO[1,5-A]PYRIDINE-3-CARBOXYLATE
C16H14N2O3 (282.10043740000003)
Methyl alpha-D-ribofuranoside 5-(4-methylbenzoate)
(E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid
C16H14N2O3 (282.10043740000003)
METHYL 5-OXO-2,3,5,6-TETRAHYDRO-1H-INDOLIZINO[6,7-B]INDOLE-11-CARBOXYLATE
C16H14N2O3 (282.10043740000003)
methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
2-Chloro-1-[[2-(triMethylsilanyl)ethoxy]Methyl]-benzimidazole
C13H19ClN2OSi (282.09551139999996)
Methyl-4-(4-chloro-1-oxobutyl)-alpha
C15H19ClO3 (282.10226539999996)
2-(3,4-dimethoxyphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde
C16H14N2O3 (282.10043740000003)
Diethyl 2,5-dioxobicyclo[2.2.2]octane-1,4-dicarboxylate
5-[(4-Methylphenyl)sulfanyl]-2,4-quinazolinediamine
1-{2-Oxo-3-[(1r)-1-(1h-Pyrrol-2-Yl)ethyl]-2h-Indol-5-Yl}urea
6-O-Methylinosine
Inosine carrying a methyl substituent on the oxygen at position 6 on the hypoxanthine ring.
N-[4-(4-oxo-2,3-dihydro-1,3-benzoxazin-2-yl)phenyl]acetamide
C16H14N2O3 (282.10043740000003)
4-(2,5-dimethylphenyl)-3-pyridin-4-yl-1H-1,2,4-triazole-5-thione
Benzyl 3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
C16H14N2O3 (282.10043740000003)
3-(2-oxo-1,3-benzoxazol-3-yl)-N-phenylpropanamide
C16H14N2O3 (282.10043740000003)
Ethyl 4-methyl-7-phenylpyrazolo[5,1-c][1,2,4]triazine-3-carboxylate
4-Morpholineacetic acid, (5-nitrofurfurylidene)hydrazide
3-(9-Oxo-9,10-dihydroacridine-2-yl)alanine
C16H14N2O3 (282.10043740000003)
1H-Pyrimido[1,2-a]quinoline-2-carboxylic acid, 1-oxo-, propyl ester
C16H14N2O3 (282.10043740000003)
1H-Pyrimido[1,2-a]quinoline-2-carboxylic acid, 1-oxo-, 1-methylethyl ester
C16H14N2O3 (282.10043740000003)
1H-Pyrimido[1,2-a]quinoline-2-acetic acid, 1-oxo-, ethyl ester
C16H14N2O3 (282.10043740000003)
3-[(4-Cyanobiphenyl-4-Yl)oxy]-N-Hydroxypropanamide
C16H14N2O3 (282.10043740000003)
4-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yloxy)-tetrahydro-pyran-2,3,5-triol
Bendazac
C16H14N2O3 (282.10043740000003)
M - Musculo-skeletal system > M02 - Topical products for joint and muscular pain > M02A - Topical products for joint and muscular pain > M02AA - Antiinflammatory preparations, non-steroids for topical use S - Sensory organs > S01 - Ophthalmologicals > S01B - Antiinflammatory agents > S01BC - Antiinflammatory agents, non-steroids C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents
Xylobiose
Xylobiose is a glycosylxylose that is D-xylopyranose having a beta-D-xylopyranosyl residue attached at position 4 via a glycosidic bond. It has a role as a bacterial metabolite. Xylobiose is a natural product found in Streptomyces ipomoeae, Chlamydomonas reinhardtii, and Streptomyces rameus with data available. A glycosylxylose that is D-xylopyranose having a beta-D-xylopyranosyl residue attached at position 4 via a glycosidic bond. Major or sole repeating unit in the main xylan chains of the plant xylans, arabinoxylans and glucuronoxylans. Isolated from Scotch pine (Pinus sylvestris). Xylobiose (1,4-β-D-Xylobiose; 1,4-D-Xylobiose) is a disaccharide?of?xylose?monomers with a β-1, 4 bond between monomers[1].
5-(3,5-Dimethoxyphenyl)-3-phenyl-1,2,4-oxadiazole
C16H14N2O3 (282.10043740000003)
N-[4-oxo-2-(2-pyridinyl)-1,2-dihydroquinazolin-3-yl]acetamide
N-(3,4-dimethylphenyl)-5-(2-furanyl)-3-isoxazolecarboxamide
C16H14N2O3 (282.10043740000003)
3-(2-Ethoxy-6-methyl-3-pyridinyl)-5-(2-pyridinyl)-1,2,4-oxadiazole
N-[(E)-1,3-benzodioxol-5-ylmethylideneamino]-2-phenylacetamide
C16H14N2O3 (282.10043740000003)
2-(2-Furanyl)-3,5-dimethyl-4-oxido-6-phenylpyrazin-1-ium 1-oxide
C16H14N2O3 (282.10043740000003)
1-[2-(2,5-Dimethylpyrrol-1-yl)-4-nitrophenyl]imidazole
2,6-diamino-4-(1-phenylethyl)-4H-thiopyran-3,5-dicarbonitrile
5-methyl-N-(5-methyl-2-phenyl-3-pyrazolyl)-3-isoxazolecarboxamide
N-(3-carbamoyl-5-propyl-2-thiophenyl)-2-oxolanecarboxamide
N-(4-ethylphenyl)-5-(2-furanyl)-3-isoxazolecarboxamide
C16H14N2O3 (282.10043740000003)
1-(3,4-Dihydroxyphenyl)-2-(2-methyl-1-benzimidazolyl)ethanone
C16H14N2O3 (282.10043740000003)
3-[(E)-3-anilino-3-oxoprop-1-enyl]-N-hydroxybenzamide
C16H14N2O3 (282.10043740000003)
4-(1-phenylethyl)-3-pyridin-4-yl-1H-1,2,4-triazole-5-thione
2-(4-Morpholinyl)-10-pyridazino[6,1-b]quinazolinone
N-cyano-N-[2-(trifluoromethyl)phenyl]pyrrolidine-1-carboximidamide
2-[3-[(3,3-Dimethyloxiran-2-yl)methyl]-4,6-dihydroxy-2-methoxyphenyl]acetic acid
9-[(2R,5R)-3-hydroxy-5-(hydroxymethyl)-4-methoxyoxolan-2-yl]-1H-purin-6-one
3-carboxy-4-methyl-5-(4-oxopentyl)-2-furanpropanoic acid
3'-Azido-3'-deoxy-5-methylcytidine
3'-Azido-3'-deoxy-5-methylcytidine (CS-92) is a potent xenotropic murine leukemia-related retrovirus (XMRV) inhibitor with a CC50 of 43.5 μM in MCF-7 cells. 3'-Azido-3'-deoxy-5-methylcytidine also inhibits HIV-1 reverse transcriptase with an EC50 of 0.06 μM in peripheral blood mononuclear (PBM) cells[1]. 3'-Azido-3'-deoxy-5-methylcytidine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
(6s)-8-bromo-3,7,7-trimethyl-11-methylidenespiro[5.5]undec-2-ene
6-(2-hydroxy-3-methoxy-5-oxofuran-2-yl)-1,3,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-one
3-(hydroxymethyl)-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one
C16H14N2O3 (282.10043740000003)
3-ethoxy-5-hydroxy-7-methoxy-4-(methoxymethyl)-6-methyl-3h-2-benzofuran-1-one
(2r,3r,4r,5r,6s)-2-{[(1z)-2-(4-hydroxyphenyl)ethenyl]oxy}-6-methyloxane-3,4,5-triol
(2r,3r,4s,5r)-4-{[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}oxane-2,3,5-triol
(1's,2s,3's,6'r,7'r,9'r)-6'-hydroxy-3-methoxy-3',7',9'-trimethyl-5',8'-dioxaspiro[furan-2,4'-tricyclo[4.2.1.0³,⁷]nonan]-5-one
(3s)-3-(hydroxymethyl)-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one
C16H14N2O3 (282.10043740000003)