Exact Mass: 163.0242622

Exact Mass Matches: 163.0242622

Found 118 metabolites which its exact mass value is equals to given mass value 163.0242622, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

N-Acetyl-D-cysteine

2-[(1-Hydroxyethylidene)amino]-3-sulphanylpropanoic acid

C5H9NO3S (163.03031239999999)


R - Respiratory system > R05 - Cough and cold preparations > R05C - Expectorants, excl. combinations with cough suppressants > R05CB - Mucolytics V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AB - Antidotes COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C78273 - Agent Affecting Respiratory System > C74536 - Mucolytic Agent D019141 - Respiratory System Agents > D005100 - Expectorants D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D000975 - Antioxidants > D016166 - Free Radical Scavengers D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7]. Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7].

   

tiopronin

2-[(1-hydroxy-2-sulfanylpropylidene)amino]acetic acid

C5H9NO3S (163.03031239999999)


Same as: D01430 Tiopronin is a diffusible antioxidant, an antidote to heavy metal poisoning and a radioprotective agent. Tiopronin can control the rate of cystine precipitation and excretion and has the potential for cystinuria, rheumatoid arthritis and hepatic disorders[1][2].

   

tiopronin

tiopronin

C5H9NO3S (163.03031239999999)


G - Genito urinary system and sex hormones > G04 - Urologicals > G04B - Urologicals C78275 - Agent Affecting Blood or Body Fluid Same as: D01430 Tiopronin is a diffusible antioxidant, an antidote to heavy metal poisoning and a radioprotective agent. Tiopronin can control the rate of cystine precipitation and excretion and has the potential for cystinuria, rheumatoid arthritis and hepatic disorders[1][2].

   

Acetylcysteine

Bristol myers squibb brand OF acetylcysteine sodium salt

C5H9NO3S (163.03031239999999)


N-Acetyl-L-cysteine (NAC) or N-Acetylcysteine is the N-acetyl derivative of the amino acid L-cysteine and is a precursor in the formation of the antioxidant glutathione in the body. N-Acetylcysteine, belongs to the class of organic compounds known as N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. N-Acetyl-L-cysteine can also be classified as an alpha amino acid or a derivatized alpha amino acid. Technically, N-Acetyl-L-cysteine is a biologically available N-terminal capped form of the proteinogenic alpha amino acid L-cysteine. N-acetyl amino acids can be produced either via direct synthesis of specific N-acetyltransferases or via the proteolytic degradation of N-acetylated proteins by specific hydrolases. N-terminal acetylation of proteins is a widespread and highly conserved process in eukaryotes that is involved in protection and stability of proteins (PMID: 16465618). About 85\\\\% of all human proteins and 68\\\\% of all yeast proteins are acetylated at their N-terminus (PMID: 21750686). Several proteins from prokaryotes and archaea are also modified by N-terminal acetylation. The majority of eukaryotic N-terminal-acetylation reactions occur through N-acetyltransferase enzymes or NAT’s (PMID: 30054468). These enzymes consist of three main oligomeric complexes NatA, NatB, and NatC, which are composed of at least a unique catalytic subunit and one unique ribosomal anchor. The substrate specificities of different NAT enzymes are mainly determined by the identities of the first two N-terminal residues of the target protein. The human NatA complex co-translationally acetylates N-termini that bear a small amino acid (A, S, T, C, and occasionally V and G) (PMID: 30054468). NatA also exists in a monomeric state and can post-translationally acetylate acidic N-termini residues (D-, E-). NatB and NatC acetylate N-terminal methionine with further specificity determined by the identity of the second amino acid. . N-acetylated amino acids, such as N-acetylcysteine can be released by an N-acylpeptide hydrolase from peptides generated by proteolytic degradation (PMID: 16465618). In addition to the NAT enzymes and protein-based acetylation, N-acetylation of free cysteine can also occur. The enzyme known as cysteine-S-conjugate N-acetyltransferase (EC 2.3.1.80) catalyzes the transfer of the acetyl group of acetyl CoA to the amino group of cysteine. This enzyme is an important participant in glutathione metabolism and the production of glutathione. The thiol (sulfhydryl) group in N-Acetylcysteine confers antioxidant effects and is able to reduce free radicals. N-Acetylcysteine is a pharmacological agent used in the management of paracetamol (acetaminophen) overdoses. When acetaminophen is taken in large quantities, a minor metabolite called N-acetyl-p-benzoquinone imine (NAPQI) accumulates within the body. NAPQI is normally conjugated by glutathione, but when taken in excess, the bodys glutathione reserves are not sufficient to deactivate the toxic NAPQI. In the treatment of acetaminophen overdose, N-acetylcysteine acts to maintain or replenish depleted glutathione reserves in the liver and enhance non-toxic metabolism of acetaminophen. These actions serve to protect liver cells from NAPQI toxicity. For this particular indication, N-acetylcysteine is available under the trade names Mucomyst (Bristol-Myers Squibb) and Parvolex (GSK). N-Acetylcysteine is also used as a mucolytic agent to reduce the viscosity of mucous secretions. It has also been shown to have antiviral effects in patients with HIV due to inhibition of viral stimulation by reactive oxygen intermediates. Acetylcysteine has been studied for a number of psychiatric disorders. There is tentative evidence for N-acetylcysteine being useful in the treatment of Alzheimers disease, autism, bipolar disorder, drug-induced neuropathy, major depressive disorder, obsessive-compulsive disord... R - Respiratory system > R05 - Cough and cold preparations > R05C - Expectorants, excl. combinations with cough suppressants > R05CB - Mucolytics V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AB - Antidotes COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C78273 - Agent Affecting Respiratory System > C74536 - Mucolytic Agent D019141 - Respiratory System Agents > D005100 - Expectorants D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D000975 - Antioxidants > D016166 - Free Radical Scavengers Effective inhibitor of enzymic browning in foods [DFC] D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7]. Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7].

   

2-Chloroquinoline

2-Chloroquinoline

C9H6ClN (163.0188746)


   

Mercaptopropionylglycine

2-[(1-Hydroxy-3-sulphanylpropylidene)amino]acetic acid

C5H9NO3S (163.03031239999999)


   

2-Hydroxy-5-trifluoromethylpyridine

2-Hydroxy-5-trifluoromethylpyridine

C6H4F3NO (163.02449699999997)


   

7-Carbamoyl-hept-2t-en-4,6-diinsaeure|7-carbamoyl-hept-2t-ene-4,6-diynoic acid|Hexen-1trans-diin-3,5-dicarbonsaeure-1,6-monoamid-6

7-Carbamoyl-hept-2t-en-4,6-diinsaeure|7-carbamoyl-hept-2t-ene-4,6-diynoic acid|Hexen-1trans-diin-3,5-dicarbonsaeure-1,6-monoamid-6

C8H5NO3 (163.02694200000002)


   

(E)-beta-chloro-alpha-phenylacrylonitrile|3-Chlor-2-phenyl-propennitril, cis|3-chloro-2-phenylacrylonitrile|3trans-Chlor-2-phenyl-acrylsaeurenitril|cis-3-Chlor-2-phenyl-propennitril|cis-beta-Chlor-alpha-phenyl-acrylnitril|E-2-Phenyl-3-chloracrylnitril

(E)-beta-chloro-alpha-phenylacrylonitrile|3-Chlor-2-phenyl-propennitril, cis|3-chloro-2-phenylacrylonitrile|3trans-Chlor-2-phenyl-acrylsaeurenitril|cis-3-Chlor-2-phenyl-propennitril|cis-beta-Chlor-alpha-phenyl-acrylnitril|E-2-Phenyl-3-chloracrylnitril

C9H6ClN (163.0188746)


   

1-oxo-1,4-thiazinane-3-carboxylic acid

1-oxo-1,4-thiazinane-3-carboxylic acid

C5H9NO3S (163.03031239999999)


   
   

Acetylcysteine

N-Acetyl-L-cysteine

C5H9NO3S (163.03031239999999)


R - Respiratory system > R05 - Cough and cold preparations > R05C - Expectorants, excl. combinations with cough suppressants > R05CB - Mucolytics V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AB - Antidotes An N-acetyl-L-amino acid that is the N-acetylated derivative of the natural amino acid L-cysteine. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C78273 - Agent Affecting Respiratory System > C74536 - Mucolytic Agent D019141 - Respiratory System Agents > D005100 - Expectorants D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D000975 - Antioxidants > D016166 - Free Radical Scavengers D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7]. Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor[1]. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases[5]. Acetylcysteine induces cell apoptosis[2][3]. Acetylcysteine also has anti-influenza virus activities[7].

   
   

Isatoic anhydride

2H-3,1-Benzoxazine-2,4(1H)-dione

C8H5NO3 (163.02694200000002)


CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3042; ORIGINAL_PRECURSOR_SCAN_NO 3041 D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D065093 - beta-Lactamase Inhibitors D004791 - Enzyme Inhibitors ORIGINAL_PRECURSOR_SCAN_NO 3022; CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3023 CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3023; ORIGINAL_PRECURSOR_SCAN_NO 3022 CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2968; ORIGINAL_PRECURSOR_SCAN_NO 2966 CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3033; ORIGINAL_PRECURSOR_SCAN_NO 3032 CONFIDENCE standard compound; INTERNAL_ID 1142; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3044; ORIGINAL_PRECURSOR_SCAN_NO 3043

   

N-Acetyl-cysteine; LC-tDDA; CE10

N-Acetyl-cysteine; LC-tDDA; CE10

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; LC-tDDA; CE20

N-Acetyl-cysteine; LC-tDDA; CE20

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; LC-tDDA; CE30

N-Acetyl-cysteine; LC-tDDA; CE30

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; LC-tDDA; CE40

N-Acetyl-cysteine; LC-tDDA; CE40

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; AIF; CE0; MS2Dec

N-Acetyl-cysteine; AIF; CE0; MS2Dec

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; AIF; CE10; MS2Dec

N-Acetyl-cysteine; AIF; CE10; MS2Dec

C5H9NO3S (163.03031239999999)


   

N-Acetyl-cysteine; AIF; CE30; MS2Dec

N-Acetyl-cysteine; AIF; CE30; MS2Dec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE0; CorrDec

Acetyl-cysteine; AIF; CE0; CorrDec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE10; CorrDec

Acetyl-cysteine; AIF; CE10; CorrDec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE30; CorrDec

Acetyl-cysteine; AIF; CE30; CorrDec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE0; MS2Dec

Acetyl-cysteine; AIF; CE0; MS2Dec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE10; MS2Dec

Acetyl-cysteine; AIF; CE10; MS2Dec

C5H9NO3S (163.03031239999999)


   

Acetyl-cysteine; AIF; CE30; MS2Dec

Acetyl-cysteine; AIF; CE30; MS2Dec

C5H9NO3S (163.03031239999999)


   
   

5-Hydroxyisoindoline-1,3-dione

5-Hydroxyisoindoline-1,3-dione

C8H5NO3 (163.02694200000002)


   

3-Chloroquinoline

3-Chloroquinoline

C9H6ClN (163.0188746)


   

2-(4-1,2,3-THIADIAZOLYL)PYRIDINE

2-(4-1,2,3-THIADIAZOLYL)PYRIDINE

C7H5N3S (163.020417)


   

Carsalam

Carsalam

C8H5NO3 (163.02694200000002)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic

   

3-Cyano-4-hydroxybenzoic acid

3-Cyano-4-hydroxybenzoic acid

C8H5NO3 (163.02694200000002)


   

6-(Trifluoromethyl)pyridin-3-ol

6-(Trifluoromethyl)pyridin-3-ol

C6H4F3NO (163.02449699999997)


   

4-(Trifluoromethyl)-3-pyridinol

4-(Trifluoromethyl)-3-pyridinol

C6H4F3NO (163.02449699999997)


   

FURO[2,3-C]PYRIDINE-2-CARBOXYLIC ACID

FURO[2,3-C]PYRIDINE-2-CARBOXYLIC ACID

C8H5NO3 (163.02694200000002)


   
   

3-Chloroisoquinoline

3-Chloroisoquinoline

C9H6ClN (163.0188746)


   

4-Chloroisoquinoline

4-Chloroisoquinoline

C9H6ClN (163.0188746)


   

2-Hydroxy-3-trifluoromethylpyridine

2-Hydroxy-3-trifluoromethylpyridine

C6H4F3NO (163.02449699999997)


   

3-(4-1,2,3-THIADIAZOLYL)PYRIDINE

3-(4-1,2,3-THIADIAZOLYL)PYRIDINE

C7H5N3S (163.020417)


   

4-(1,2,3-THIADIAZOL-4-YL)PYRIDINE

4-(1,2,3-THIADIAZOL-4-YL)PYRIDINE

C7H5N3S (163.020417)


   

5-(2-FURYL)ISOXAZOLE-3-CARBALDEHYDE

5-(2-FURYL)ISOXAZOLE-3-CARBALDEHYDE

C8H5NO3 (163.02694200000002)


   
   

7-Chloroisoquinoline

7-Chloroisoquinoline

C9H6ClN (163.0188746)


   

2-HYDROXY-5-(TRIFLUOROMETHYL)PYRIDINE

2-HYDROXY-5-(TRIFLUOROMETHYL)PYRIDINE

C6H4F3NO (163.02449699999997)


   

Benzo[d]oxazole-4-carboxylic acid

Benzo[d]oxazole-4-carboxylic acid

C8H5NO3 (163.02694200000002)


   
   

2-(Trifluoromethyl)pyridine 1-oxide

2-(Trifluoromethyl)pyridine 1-oxide

C6H4F3NO (163.02449699999997)


   

5-Chloroisoquinoline

5-Chloroisoquinoline

C9H6ClN (163.0188746)


   
   

1,3-Isobenzofurandione,4-amino-

1,3-Isobenzofurandione,4-amino-

C8H5NO3 (163.02694200000002)


   

2-amino-3,5-Dicyanoacetophenone

2-amino-3,5-Dicyanoacetophenone

C7H5N3S (163.020417)


   

Furo[3,2-b]pyridine-5-carboxylic acid

Furo[3,2-b]pyridine-5-carboxylic acid

C8H5NO3 (163.02694200000002)


   
   

N-Methyl-2-thiophenemethanamine hydrochloride

N-Methyl-2-thiophenemethanamine hydrochloride

C6H10ClNS (163.022245)


   

2-amino-6-chloro-4-pyrimidinol hydrate, 95

2-amino-6-chloro-4-pyrimidinol hydrate, 95

C4H6ClN3O2 (163.0148526)


   

phenyl N-(oxomethylidene)carbamate

phenyl N-(oxomethylidene)carbamate

C8H5NO3 (163.02694200000002)


   

2,1-Benzoxazole-3-carboxylic acid

2,1-Benzoxazole-3-carboxylic acid

C8H5NO3 (163.02694200000002)


   

BENZO[D]OXAZOLE-7-CARBOXYLIC ACID

BENZO[D]OXAZOLE-7-CARBOXYLIC ACID

C8H5NO3 (163.02694200000002)


   
   

Benzooxazole-2-carboxylic acid

Benzooxazole-2-carboxylic acid

C8H5NO3 (163.02694200000002)


   

1-Chloroisoquinoline

1-Chloroisoquinoline

C9H6ClN (163.0188746)


   

4-chlorocinnamonitrile

4-chlorocinnamonitrile

C9H6ClN (163.0188746)


   

Furo[3,2-b]pyridine-6-carboxylic acid

Furo[3,2-b]pyridine-6-carboxylic acid

C8H5NO3 (163.02694200000002)


   

2,3,6-Trifluoro-4-methoxypyridine

2,3,6-Trifluoro-4-methoxypyridine

C6H4F3NO (163.02449699999997)


   
   

Benzo[d]oxazole-6-carboxylic acid

Benzo[d]oxazole-6-carboxylic acid

C8H5NO3 (163.02694200000002)


   
   

8-Chloroisoquinoline

8-Chloroisoquinoline

C9H6ClN (163.0188746)


   

5-methyl-2-Thiophenemethanamine

5-methyl-2-Thiophenemethanamine

C6H10ClNS (163.022245)


   

2-(Trifluoromethyl)-4-pyridinol

2-(Trifluoromethyl)-4-pyridinol

C6H4F3NO (163.02449699999997)


   
   

Benzoxazole-5-carboxylic Acid

Benzoxazole-5-carboxylic Acid

C8H5NO3 (163.02694200000002)


   

3-Chloro-3-phenyl-acrylonitrile

3-Chloro-3-phenyl-acrylonitrile

C9H6ClN (163.0188746)


   

2-(Trifluoromethyl)-3-pyridinol

2-(Trifluoromethyl)-3-pyridinol

C6H4F3NO (163.02449699999997)


   

2-Chloro-3-phenylpropenenitrile

2-Chloro-3-phenylpropenenitrile

C9H6ClN (163.0188746)


   

2,1-Benzisoxazole-4-carboxylicacid(9CI)

2,1-Benzisoxazole-4-carboxylicacid(9CI)

C8H5NO3 (163.02694200000002)


   

2-[(3-CHLOROPROPYL)SULFANYL]PROPANENITRILE

2-[(3-CHLOROPROPYL)SULFANYL]PROPANENITRILE

C6H10ClNS (163.022245)


   

Sodium (Z)-1-cyano-3-ethoxy-3-oxoprop-1-en-2-olate

Sodium (Z)-1-cyano-3-ethoxy-3-oxoprop-1-en-2-olate

C6H6NNaO3 (163.0245366)


   

2-(Aminomethyl)-5-methylthiophene hydrochloride

(5-Methylthiophen-2-yl)methanamine hydrochloride

C6H10ClNS (163.022245)


   

Furo[3,2-c]pyridine-2-carboxylic acid

Furo[3,2-c]pyridine-2-carboxylic acid

C8H5NO3 (163.02694200000002)


   

3-(trifluoromethyl)pyridine 1-oxide

3-(trifluoromethyl)pyridine 1-oxide

C6H4F3NO (163.02449699999997)


   

1,2-benzoxazole-3-carboxylic acid

1,2-benzoxazole-3-carboxylic acid

C8H5NO3 (163.02694200000002)


   

6-Chloroquinoline

6-Chloroquinoline

C9H6ClN (163.0188746)


   

6-Chloroisoquinoline

6-Chloroisoquinoline

C9H6ClN (163.0188746)


   

4-cyano-2-hydroxybenzoic acid

4-cyano-2-hydroxybenzoic acid

C8H5NO3 (163.02694200000002)


   

4-AMino-2-fluorophenolHydrochloride

4-AMino-2-fluorophenolHydrochloride

C6H7ClFNO (163.0200174)


   
   

7-Chloroquinoline

7-Chloroquinoline

C9H6ClN (163.0188746)


   

5-Chloroquinoline

5-Chloroquinoline

C9H6ClN (163.0188746)


   
   

Furo[2,3-c]pyridine-5-carboxylic acid

Furo[2,3-c]pyridine-5-carboxylic acid

C8H5NO3 (163.02694200000002)


   

4-Chloroquinoline

4-Chloroquinoline

C9H6ClN (163.0188746)


   

3-Fluoro-2-methoxypyridine hydrochloride

3-Fluoro-2-methoxypyridine hydrochloride

C6H7ClFNO (163.0200174)


   

1-(Difluoromethyl)-4-nitro-1H-pyrazole

1-(Difluoromethyl)-4-nitro-1H-pyrazole

C4H3F2N3O2 (163.0193322)


   

8-Chloroquinoline

8-Chloroquinoline

C9H6ClN (163.0188746)


   

3,4-(Methylenedioxy)phenyl isocyanate

3,4-(Methylenedioxy)phenyl isocyanate

C8H5NO3 (163.02694200000002)


   

4-AMINO-3-FLUOROPHENOL HYDROCHLORIDE

4-AMINO-3-FLUOROPHENOL HYDROCHLORIDE

C6H7ClFNO (163.0200174)


   

2-Hydroxy-4-(trifluoromethyl)pyridine

2-Hydroxy-4-(trifluoromethyl)pyridine

C6H4F3NO (163.02449699999997)


   

2,2,2-trifluoro-1-(1H-pyrrol-3-yl)ethanone

2,2,2-trifluoro-1-(1H-pyrrol-3-yl)ethanone

C6H4F3NO (163.02449699999997)


   

5-(Trifluoromethyl)-3-pyridinol

5-(Trifluoromethyl)-3-pyridinol

C6H4F3NO (163.02449699999997)


   

2-fluoro-6-difluoromethoxy pyridine

2-fluoro-6-difluoromethoxy pyridine

C6H4F3NO (163.02449699999997)


   
   

N-(3-Mercapto-1-oxopropyl)glycine

N-(3-Mercapto-1-oxopropyl)glycine

C5H9NO3S (163.03031239999999)


   

Aluminum subacetate

Aluminum subacetate

C4H8AlO5 (163.0187128)


   

3-Oxoisoapionate

3-Oxoisoapionate

C5H7O6- (163.0242622)


   

aldehydo-L-arabinuronate

aldehydo-L-arabinuronate

C5H7O6- (163.0242622)


   
   

2-Dehydro-D-xylonate

2-Dehydro-D-xylonate

C5H7O6- (163.0242622)


   

N-carbamoyl-L-cysteinate(1-)

N-carbamoyl-L-cysteinate(1-)

C4H7N2O3S- (163.0177372)


The L-alpha-amino acid anion that is the anion formed by loss of a proton from the carboxy group of N-carbamoyl-L-cysteine; major species present at pH 7.3.

   
   

(2R)-2,4-dihydroxy-2-(hydroxymethyl)-3-oxobutanoate

(2R)-2,4-dihydroxy-2-(hydroxymethyl)-3-oxobutanoate

C5H7O6- (163.0242622)


   

1,4-thiazane-3-carboxylicacid s-oxide

NA

C5H9NO3S (163.03031239999999)


{"Ingredient_id": "HBIN001558","Ingredient_name": "1,4-thiazane-3-carboxylicacid s-oxide","Alias": "NA","Ingredient_formula": "C5H9NO3S","Ingredient_Smile": "C1CS(=O)CC(N1)C(=O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "21314","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(2e)-7-(c-hydroxycarbonimidoyl)hept-2-en-4,6-diynoic acid

(2e)-7-(c-hydroxycarbonimidoyl)hept-2-en-4,6-diynoic acid

C8H5NO3 (163.02694200000002)


   

1-hydroxy-1,2-bis(prop-1-en-1-yl)disulfanium

1-hydroxy-1,2-bis(prop-1-en-1-yl)disulfanium

[C6H11OS2]+ (163.0251296)


   

7-(c-hydroxycarbonimidoyl)hept-2-en-4,6-diynoic acid

7-(c-hydroxycarbonimidoyl)hept-2-en-4,6-diynoic acid

C8H5NO3 (163.02694200000002)


   

(2r)-2-[(1-hydroxyethylidene)amino]-3-sulfanylpropanoic acid

(2r)-2-[(1-hydroxyethylidene)amino]-3-sulfanylpropanoic acid

C5H9NO3S (163.03031239999999)