Exact Mass: 322.99383760000006

Exact Mass Matches: 322.99383760000006

Found 83 metabolites which its exact mass value is equals to given mass value 322.99383760000006, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

O-Ethyl O-(4-nitrophenyl) phenylphosphonothioate

Ethoxy-(4-nitrophenoxy)-phenyl-sulphanylidene-$l^{5}-phosphane

C14H14NO4PS (323.03811340000004)

D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals

Benodanil

C13H10INO (322.98071200000004)

CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3920; ORIGINAL_PRECURSOR_SCAN_NO 3919 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8439; ORIGINAL_PRECURSOR_SCAN_NO 8437 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3917; ORIGINAL_PRECURSOR_SCAN_NO 3915 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8428; ORIGINAL_PRECURSOR_SCAN_NO 8426 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8422; ORIGINAL_PRECURSOR_SCAN_NO 8419 INTERNAL_ID 203; CONFIDENCE standard compound; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8439; ORIGINAL_PRECURSOR_SCAN_NO 8437 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3954; ORIGINAL_PRECURSOR_SCAN_NO 3952 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3950; ORIGINAL_PRECURSOR_SCAN_NO 3946 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8451; ORIGINAL_PRECURSOR_SCAN_NO 8448 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3916; ORIGINAL_PRECURSOR_SCAN_NO 3913 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8442; ORIGINAL_PRECURSOR_SCAN_NO 8438 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3917; ORIGINAL_PRECURSOR_SCAN_NO 3914 CONFIDENCE standard compound; INTERNAL_ID 203; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8370; ORIGINAL_PRECURSOR_SCAN_NO 8367

N-(1,3-Benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide

C15H11Cl2NO3 (323.0115956000001)

Alda-1 is a potent and selective ALDH2 agonist, which activates wild-type ALDH2 and restores near wild-type activity to ALDH2*2.

N-(1,3-Benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide

N-(2H-1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzene-1-carboximidic acid

C15H11Cl2NO3 (323.0115956000001)

CONFIDENCE Transformation product, tentative ID (Level 3 structure); INTERNAL_ID 2003

PRZ_M323a

C12H12Cl3NO3 (322.9882732000001)

CONFIDENCE Transformation product, tentative ID (Level 3 structure); INTERNAL_ID 2004

MMV676358

C11H7N5BrCl (322.95733120000006)

N-(3,5-DICHLOROBENZENESULFONYL)-L-PROLINE

C11H11Cl2NO4S (322.97858260000004)

N-ACETYL-ALPHA-D-GLUCOSAMINE 6-PHOSPHATE DISODIUM SALT

C8H15NNaO9P (323.038211)

2-(2-CHLORO-ACETYLAMINO)-4-PHENYL-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER

C15H14ClNO3S (323.03828840000006)

3-(Naphthalene-2-sulfonyl)-thiazolidine-2-carboxylic acid

C14H13NO4S2 (323.0285978)

4-[(4-Bromo-3-fluorophenyl)sulfonyl]morpholine

C10H11BrFNO3S (322.9627008)

1-(3,4-Dichlorobenzyl)-4-piperidine-carboxylic acid hydrochloride

C13H16Cl3NO2 (323.0246566)

bismuth subnitrate monohydrate

BiH4NO6 (322.9842504)

6-chloro-3-[(3,5-dichlorophenyl)methylidene]-1H-indol-2-one

C15H8Cl3NO (322.9671448)

1-diethoxyphosphorylsulfanyl-4-nitrobenzene

C10H14NO7PS (323.0228584000001)

N-benzyl-5-bromo-2-chlorobenzamide

C14H11BrClNO (322.9712486)

ETHYL 3-AMINO-4-(ISOPROPYLSULFONYL)-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE

C11H17NO4S3 (323.0319682)

4-BROMOTRIPHENYLAMINE

C18H14BrN (323.03095440000004)

METHYL 3-(4-CHLOROPHENYL)-4-CYANO-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE

C14H10ClNO2S2 (322.984147)

2-(1-((4-BROMOPHENYL)IMINO)ETHYL)-4-CHLOROPHENOL

C14H11BrClNO (322.9712486)

2-Bromo-N,N-diphenylaniline

C18H14BrN (323.03095440000004)

2-FORMYL-4-NITROPHENYL 2-CHLORO-6-FLUOROBENZOATE

C14H7ClFNO5 (322.9996774)

(2-Amino-5-iodophenyl)(phenyl)methanone

C13H10INO (322.98071200000004)

n-acetylglucosamine 6-sulfate sodium salt

C8H14NNaO9S (323.02869540000006)

ETHYL 4-(4-BROMOBENZOYL)-3-ISOXAZOLECARBOXYLATE

C13H10BrNO4 (322.97931600000004)

1-BOC-4-BROMO-3-FORMYLINDOLE

C14H14BrNO3 (323.0156994)

1-BOC-5-BROMO-3-FORMYLINDOLE

C14H14BrNO3 (323.0156994)

2-Benzyl-5-bromoisoindoline hydrochloride (1:1)

C15H15BrClN (323.00763200000006)

N-Cbz-3-bromo-4-fluoroaniline

C14H11BrFNO2 (322.9957138)

3-Bromo-N,N-diphenylaniline

C18H14BrN (323.03095440000004)

AA 41612

C12H15Cl2NO3S (323.014966)

N-acetyl-d-glucosamine 6-phosphate disodium salt

D-Glucopyranose, 2-(acetylamino)-2-deoxy-, 6-(dihydrogen phosphate), disodium salt

C8H15NNaO9P (323.038211)

Glycogen Metabolism: In mammals, GlcNAc-6-P plays a key role in the synthesis of glycogen, a storage form of glucose in the body. It is formed from glucose-6-phosphate by the enzyme glucosamine-6-phosphate synthase. GlcNAc-6-P is then converted to UDP-N-acetylglucosamine (UDP-GlcNAc), which is essential for the addition of GlcNAc residues to the growing glycogen chain during glycogen synthesis. Pentose Phosphate Pathway (PPP): GlcNAc-6-P can enter the PPP, a metabolic pathway that operates parallel to glycolysis. In the PPP, it is involved in the production of NADPH, which is important for reductive biosynthesis and antioxidant defense, and ribose-5-phosphate, a precursor for nucleotide synthesis. Cell Wall Synthesis in Bacteria and Fungi: In certain bacteria and fungi, GlcNAc-6-P is a precursor for the synthesis of peptidoglycan and chitin, respectively. Peptidoglycan is a major component of the cell wall in bacteria, providing structural support and protection. Chitin, found in the cell walls of fungi and the exoskeletons of arthropods, also plays a structural role. Other Metabolic Roles: GlcNAc-6-P is also involved in the synthesis of other complex carbohydrates and glycoproteins. It serves as a precursor for the synthesis of hyaluronic acid and keratan sulfate, important components of connective tissues and the extracellular matrix. Regulation of Metabolic Pathways: The levels of GlcNAc-6-P can regulate the activity of key enzymes in glucose metabolism. For example, high levels of GlcNAc-6-P can inhibit the enzyme phosphofructokinase-1 (PFK-1), a key regulatory step in glycolysis, thereby modulating the flux of glucose through this pathway. D-Glucopyranose, 2-(acetylamino)-2-deoxy-, 6-(dihydrogen phosphate), disodium salt. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=102029-88-9 (retrieved 2024-08-06) (CAS RN: 102029-88-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

H-9 dihydrochloride

C11H15Cl2N3O2S (323.026199)

H-9 Dihydrochloride is a PKA (protein kinase) inhibitor. H-9 Dihydrochloride (10 μM) significantly reduces the excitatory response to 5-HT. H-9 Dihydrochloride also has a direct effect on pharyngeal activity. H-9 Dihydrochloride inhibits signal-transduction and cell growth in EGF (epidermal growth factor)-dependent epithelial cell lines[1][2][3].