Exact Mass: 692.380528

Exact Mass Matches: 692.380528

Found 30 metabolites which its exact mass value is equals to given mass value 692.380528, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Opiorphin

(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-4-(C-hydroxycarbonimidoyl)butylidene]amino}-5-carbamimidamido-1-hydroxypentylidene]amino}-1-hydroxy-3-phenylpropylidene]amino}-1,3-dihydroxypropylidene]amino}-5-carbamimidamidopentanoic acid

C29H48N12O8 (692.3717888)


Opiorphin is an endogenous 5-residue opioid peptide (Gln-Arg-Phe-Ser-Arg) first isolated from human saliva. Initial research with mice shows the compound has a painkilling effect greater than that of morphine. It works by stopping the normal breakdown of enkephalins, natural pain-killing opioids in the spinal cord. Opiorphin originates from the N-terminal region of the protein PROL1 (proline rich, lacrimal 1) and inhibits three proteases: neutral ecto-endopeptidase (MME), ecto-aminopeptidase N (ANPEP) and a dipeptidyl peptidase DPP3. This protease inhibitory action extends the duration of enkephalins, which are natural pain killers that are released in response to specific potentially painful stimuli. Opiorphin, an opioid peptide, is a potent enkephalin-inactivating zinc ectopeptidases in human inhibitor. Opiorphin inhibits two enkephalin-catabolizing ectoenzymes, human neutral ecto-endopeptidase, hNEP (EC 3.4.24.11) with an IC50 value of 11 μM, and human ecto-aminopeptidase, hAP-N (EC 3.4.11.2). Opiorphin displays potent analgesic activity by activating endogenous opioid-dependent transmission[1][2].

   
   

16beta-acetoxy-3-O-beta-D-xylopyranosyl-22,25-epoxyholosta-9(11)-ene-3beta,12alpha,17alpha-triol|nobiliside C

16beta-acetoxy-3-O-beta-D-xylopyranosyl-22,25-epoxyholosta-9(11)-ene-3beta,12alpha,17alpha-triol|nobiliside C

C37H56O12 (692.3771576)


   
   

3-O-beta-D-glucopyranosylplatycogenic acid A lactone methyl ester

3-O-beta-D-glucopyranosylplatycogenic acid A lactone methyl ester

C37H56O12 (692.3771576)


   

Antibiotic PD 118576A1

Antibiotic PD 118576A1

C37H56O12 (692.3771576)


   

3alpha-Methacryloyloxy-2beta-hydroxy-ent-labd-7-en-15-oic acid-2-O-beta-fucopyranoside methyl ester triacetate

3alpha-Methacryloyloxy-2beta-hydroxy-ent-labd-7-en-15-oic acid-2-O-beta-fucopyranoside methyl ester triacetate

C37H56O12 (692.3771576)


   

Antibiotic PD 118576A2

Antibiotic PD 118576A2

C37H56O12 (692.3771576)


   

(3beta,5alpha,6beta,8beta,15alpha,16beta)-3-O-[2,4-Di-O-methyl-beta-D-xylopyranoside],15-sulfate,Cholestane-3,6,8,15,16-pentol

(3beta,5alpha,6beta,8beta,15alpha,16beta)-3-O-[2,4-Di-O-methyl-beta-D-xylopyranoside],15-sulfate,Cholestane-3,6,8,15,16-pentol

C34H60O12S (692.380528)


   

PKODA-PG

1-hexadecanoyl-2-(9,12-dioxo-10E-dodecenoyl)-sn-glycero-3-phospho-(1-sn-glycerol)

C34H61O12P (692.3900435999999)


   
   
   
   
   
   

Opiorphin

Opiorphin

C29H48N12O8 (692.3717888)


Opiorphin, an opioid peptide, is a potent enkephalin-inactivating zinc ectopeptidases in human inhibitor. Opiorphin inhibits two enkephalin-catabolizing ectoenzymes, human neutral ecto-endopeptidase, hNEP (EC 3.4.24.11) with an IC50 value of 11 μM, and human ecto-aminopeptidase, hAP-N (EC 3.4.11.2). Opiorphin displays potent analgesic activity by activating endogenous opioid-dependent transmission[1][2].