Exact Mass: 178.0237

Exact Mass Matches: 178.0237

Found 199 metabolites which its exact mass value is equals to given mass value 178.0237, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

5,7-Dihydroxy-4H-1-benzopyran-4-one

4H-1-Benzopyran-4-one, 5,7-dihydroxy-

C9H6O4 (178.0266)


5,7-Dihydroxychromone is a member of chromones. 5,7-Dihydroxychromone is a natural product found in Calluna vulgaris, Leucosidea sericea, and other organisms with data available. 5,7-Dihydroxy-4H-1-benzopyran-4-one is found in nuts. 5,7-Dihydroxy-4H-1-benzopyran-4-one is isolated from peanut shells. Isolated from peanut shells. 5,7-Dihydroxy-4H-1-benzopyran-4-one is found in peanut and nuts. 5,7-Dihydroxychromone, the extract of Cudrania tricuspidata, activates Nrf2/ARE signal and exerts neuroprotective effects against 6-hydroxydopamine (6-OHDA)-induced oxidative stress and apoptosis. 5,7-Dihydroxychromone inhibits the expression of activated caspase-3 and caspase-9 and cleaved PARP in 6-OHDA-induced SH-SY5Y cells[1]. 5,7-Dihydroxychromone, the extract of Cudrania tricuspidata, activates Nrf2/ARE signal and exerts neuroprotective effects against 6-hydroxydopamine (6-OHDA)-induced oxidative stress and apoptosis. 5,7-Dihydroxychromone inhibits the expression of activated caspase-3 and caspase-9 and cleaved PARP in 6-OHDA-induced SH-SY5Y cells[1].

   

Aesculetin

6,7-dihydroxychromen-2-one

C9H6O4 (178.0266)


Aesculetin, also known as cichorigenin or cichoriin aglucon, belongs to the class of organic compounds known as 6,7-dihydroxycoumarins. These are coumarins bearing two hydroxyl groups at positions 6 and 7 of the coumarin skeleton, respectively. Aesculetin is found, on average, in the highest concentration within sherries. Aesculetin has also been detected, but not quantified, in several different foods, such as horseradish, carrots, dandelions, grape wines, and highbush blueberries. This could make aesculetin a potential biomarker for the consumption of these foods. Esculetin is a hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. It has a role as an antioxidant, an ultraviolet filter and a plant metabolite. Esculetin is a natural product found in Artemisia eriopoda, Euphorbia decipiens, and other organisms with data available. A hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. Metabolite of infected sweet potato. Aesculetin is found in many foods, some of which are root vegetables, wild carrot, sweet basil, and carrot. D020011 - Protective Agents > D000975 - Antioxidants Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CB031_Aesculetin_pos_20eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_10eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_40eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_50eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_30eV_CB000017.txt [Raw Data] CB031_Aesculetin_neg_10eV_000010.txt [Raw Data] CB031_Aesculetin_neg_20eV_000010.txt [Raw Data] CB031_Aesculetin_neg_30eV_000010.txt CONFIDENCE standard compound; ML_ID 39 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Daphnetol

7,8-dihydroxychromen-2-one

C9H6O4 (178.0266)


7,8-dihydroxycoumarin is a hydroxycoumarin. Daphnetin is a natural product found in Euphorbia dracunculoides, Rhododendron lepidotum, and other organisms with data available. Acquisition and generation of the data is financially supported in part by CREST/JST. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research Daphnetin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=486-35-1 (retrieved 2024-09-04) (CAS RN: 486-35-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

1-Phenyltetrazole-5-thiol

1-Phenyl-5-mercaptotetrazole

C7H6N4S (178.0313)


   

Caffeoquinone

3,4-dioxocinnamic acid

C9H6O4 (178.0266)


An alpha,beta-unsaturated monocarboxylic acid that is acrylic acid in which one of the olefinic hydrogens at position 3 has been replaced by a 3,4-dioxocyclohexa-1,5-dien-1-yl group.

   

3,3'-Thiobispropanoic acid

3-[(2-Carboxyethyl)sulphanyl]propanoic acid

C6H10O4S (178.03)


3,3-Thiobispropanoic acid is an antioxidant used in food packaging material Antioxidant used in food packaging materials.

   

5,7-dihydroxy-2H-chromen-2-one

5,7-dihydroxy-2H-chromen-2-one

C9H6O4 (178.0266)


   

3,7-dihydroxychromen-2-one

3,7-dihydroxychromen-2-one

C9H6O4 (178.0266)


   

4,7-Dihydroxy-2H-1-benzopyran-2-one

2H-1-Benzopyran-2-one,4,7-dihydroxy-

C9H6O4 (178.0266)


4,7-Dihydroxy-2H-1-benzopyran-2-one is found in green vegetables. 4,7-Dihydroxy-2H-1-benzopyran-2-one is a constituent of the seeds of Corchorus olitorius (Jews mallow). Constituent of the seeds of Corchorus olitorius (Jews mallow). 4,7-Dihydroxy-2H-1-benzopyran-2-one is found in tea, herbs and spices, and green vegetables.

   

2,3-Dihydroxy-5-methylthio-4-pentenoic acid

(2R,3R,4E)-2,3-Dihydroxy-5-(methylsulphanyl)pent-4-enoic acid

C6H10O4S (178.03)


2,3-Dihydroxy-5-methylthio-4-pentenoic acid (DMTPA) is a hydroxy fatty acid with a thioenolether group. DMTPA was previously an unknown potential plasma biomarker for glomerular filtration rate (GFR) but its structure has since been elucidated (PMID: 29578721). DMTPA is possibly involved in the methionine salvage pathway (MSP) and may potentially be synthesized from methylthioadenosine (MTA). MTA is a byproduct of S-adenosylmethionine (SAM) during polyamine biosynthesis.

   

1,1'-Thiocarbonyldiimidazole

1-(1H-imidazole-1-carbothioyl)-1H-imidazole

C7H6N4S (178.0313)


   

4-Chloro-1-naphthol

4-Chloronaphthalen-1-ol

C10H7ClO (178.0185)


   

4-Amino-7-chloroquinoline

7-Chloro-4-aminoquinoline

C9H7ClN2 (178.0298)


   

Acivicin

L-(AlphaS,5S)-alpha-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid

C5H7ClN2O3 (178.0145)


   

Dimethyl mercaptosuccinate

Dimethyl mercaptosuccinate, (r*,s*)-isomer

C6H10O4S (178.03)


   

Ninhydrin

2,2-dihydroxy-2,3-dihydro-1H-indene-1,3-dione

C9H6O4 (178.0266)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D011838 - Radiation-Sensitizing Agents

   

5,7-Dihydroxycoumarin

5,7-Dihydroxycoumarin

C9H6O4 (178.0266)


5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2]. 5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2].

   

5,8-dihydroxycoumarin

5,8-dihydroxycoumarin

C9H6O4 (178.0266)


   

4-Hydroxybenzofuran-5-carboxylic acid

4-Hydroxybenzofuran-5-carboxylic acid

C9H6O4 (178.0266)


   

Coryhumolide

Coryhumolide

C9H6O4 (178.0266)


   

alpha-Amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid

alpha-Amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid

C5H7ClN2O3 (178.0145)


   

3,7-dihydroxychromen-4-one

3,7-dihydroxychromen-4-one

C9H6O4 (178.0266)


A natural product found in Caesalpinia sappan.

   

6,7-Dihydroxy-4H-1-benzopyran-4-one

6,7-Dihydroxy-4H-1-benzopyran-4-one

C9H6O4 (178.0266)


   

6,7-Methylenedioxyphthalide

6,7-Methylenedioxyphthalide

C9H6O4 (178.0266)


   

7,8-dihydroxychromen-4-one

7,8-dihydroxychromen-4-one

C9H6O4 (178.0266)


   

4,8-Dihydroxycoumarin

4,8-Dihydroxycoumarin

C9H6O4 (178.0266)


   

7-chloroquinolin-4-amine

7-chloroquinolin-4-amine

C9H7ClN2 (178.0298)


   

Coumarin derivative, 1a

InChI=1/C9H6O4/c10-5-3-7(11)6-1-2-9(12)13-8(6)4-5/h1-4,10-11

C9H6O4 (178.0266)


5,7-Dihydroxycoumarin is a natural product found in Fagopyrum megacarpum, Murraya siamensis, and other organisms with data available. 5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2]. 5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2].

   

Esculetin

InChI=1\C9H6O4\c10-6-3-5-1-2-9(12)13-8(5)4-7(6)11\h1-4,10-11

C9H6O4 (178.0266)


D020011 - Protective Agents > D000975 - Antioxidants relative retention time with respect to 9-anthracene Carboxylic Acid is 0.434 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.428 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.430 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Daphnetin

Daphnetin

C9H6O4 (178.0266)


7,8-dihydroxy-2h-chromen-2-one, also known as daphnetin or 7,8-dihydroxycoumarin, is a member of the class of compounds known as 7,8-dihydroxycoumarins. 7,8-dihydroxycoumarins are coumarins bearing two hydroxyl groups at the C7- and C8-positions of the coumarin skeleton, respectively. 7,8-dihydroxy-2h-chromen-2-one is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 7,8-dihydroxy-2h-chromen-2-one can be found in chickpea and watermelon, which makes 7,8-dihydroxy-2h-chromen-2-one a potential biomarker for the consumption of these food products. CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 15 INTERNAL_ID 15; CONFIDENCE Reference Standard (Level 1) Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4].

   

6,7-dihydroxychromen-2-one

NCGC00016425-09!6,7-dihydroxychromen-2-one

C9H6O4 (178.0266)


   

6,7-dihydroxycoumarin

6,7-dihydroxycoumarin

C9H6O4 (178.0266)


Annotation level-1

   

7,8-Dihydroxycoumarin

7,8-Dihydroxycoumarin

C9H6O4 (178.0266)


Annotation level-1

   

Thiobispropanoic acid

Thiobispropanoic acid

C6H10O4S (178.03)


Annotation level-3

   

7,8-Dihydroxy-2H-chromen-2-one

7,8-Dihydroxy-2H-chromen-2-one

C9H6O4 (178.0266)


Annotation level-1

   

6,7-dihydroxychromen-2-one [IIN-based: Match]

NCGC00016425-09!6,7-dihydroxychromen-2-one [IIN-based: Match]

C9H6O4 (178.0266)


   

6,7-dihydroxychromen-2-one [IIN-based on: CCMSLIB00000845335]

NCGC00016425-09!6,7-dihydroxychromen-2-one [IIN-based on: CCMSLIB00000845335]

C9H6O4 (178.0266)


   

THIODIPROPIONIC ACID

Bis(2-carboxyethyl) sulfide

C6H10O4S (178.03)


CONFIDENCE standard compound; INTERNAL_ID 413; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2583; ORIGINAL_PRECURSOR_SCAN_NO 2581 CONFIDENCE standard compound; INTERNAL_ID 413; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2568; ORIGINAL_PRECURSOR_SCAN_NO 2565 CONFIDENCE standard compound; INTERNAL_ID 413; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2642; ORIGINAL_PRECURSOR_SCAN_NO 2639 CONFIDENCE standard compound; INTERNAL_ID 413; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2583; ORIGINAL_PRECURSOR_SCAN_NO 2580

   

7-Chloro-4-quinolinamine

4-Amino-7-chloroquinoline

C9H7ClN2 (178.0298)


   

&beta

3-[(2-carboxyethyl)sulfanyl]propanoic acid

C6H10O4S (178.03)


   

4,7-Dihydroxycoumarin

2H-1-Benzopyran-2-one,4,7-dihydroxy-

C9H6O4 (178.0266)


   

2-Chloro-6-quinolinamine

2-Chloro-6-quinolinamine

C9H7ClN2 (178.0298)


   

3-(2-thienyl)-1h-pyrazole-4-carbaldehyde

3-(2-thienyl)-1h-pyrazole-4-carbaldehyde

C8H6N2OS (178.0201)


   

5-chloroquinolin-4-amine

5-chloroquinolin-4-amine

C9H7ClN2 (178.0298)


   

2-Chloroquinolin-4-amine

2-Chloroquinolin-4-amine

C9H7ClN2 (178.0298)


   

4-chloroquinolin-2-amine

4-chloroquinolin-2-amine

C9H7ClN2 (178.0298)


   

5-pyridin-3-yl-1,3,4-thiadiazol-2-amine

5-pyridin-3-yl-1,3,4-thiadiazol-2-amine

C7H6N4S (178.0313)


   

5-Phenyl-1,3,4-oxadiazole-2(3H)-thione

5-Phenyl-1,3,4-oxadiazole-2(3H)-thione

C8H6N2OS (178.0201)


   

2,2-BIFURAN]-5-CARBOXYLIC ACID

2,2-BIFURAN]-5-CARBOXYLIC ACID

C9H6O4 (178.0266)


   

4-(4-Chlorophenyl)-1H-pyrazole

4-(4-Chlorophenyl)-1H-pyrazole

C9H7ClN2 (178.0298)


   

1-benzothiophen-5-ylboronic acid

1-benzothiophen-5-ylboronic acid

C8H7BO2S (178.026)


   

5-Chloroisoquinolin-6-amine

5-Chloroisoquinolin-6-amine

C9H7ClN2 (178.0298)


   

Benzothiophene-3-boronic acid

Benzothiophene-3-boronic acid

C8H7BO2S (178.026)


   

4-(2-furyl)-2-pyrimidinethiol

4-(2-furyl)-2-pyrimidinethiol

C8H6N2OS (178.0201)


   

Acivicin

Acivicin

C5H7ClN2O3 (178.0145)


An L-alpha-amino acid that is L-alanine in which the methyl group is replaced by a (5S)-3-chloro-4,5-dihydro-1,2-oxazol-5-yl group. A glutamine analogue antimetabolite, it interferes with glutamate metabolism and several glutamate-dependent synthetic enzymes. It is obtained as a fermentation product of Streptomyces sviceus bacteria. C471 - Enzyme Inhibitor > C2158 - Glutamine Amidotransferase Inhibitor D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

1H-Imidazole,1-(3-chlorophenyl)-

1H-Imidazole,1-(3-chlorophenyl)-

C9H7ClN2 (178.0298)


   

1-(4-CHLOROPHENYL)BIGUANIDE

1-(4-CHLOROPHENYL)BIGUANIDE

C9H7ClN2 (178.0298)


   

methyl 3-amino-1H-1,2,4-triazole-5-carboxylate,hydrochloride

methyl 3-amino-1H-1,2,4-triazole-5-carboxylate,hydrochloride

C4H7ClN4O2 (178.0258)


   

1-(1,3-THIAZOL-2-YL)-1H-PYRROLE-2-CARBALDEHYDE

1-(1,3-THIAZOL-2-YL)-1H-PYRROLE-2-CARBALDEHYDE

C8H6N2OS (178.0201)


   

2-Chloro-6-methylquinazoline

2-Chloro-6-methylquinazoline

C9H7ClN2 (178.0298)


   

2-Chloro-6-methylquinoxaline

2-Chloro-6-methylquinoxaline

C9H7ClN2 (178.0298)


   

2-Chloro-3-aminoquinoline

2-Chloro-3-aminoquinoline

C9H7ClN2 (178.0298)


   

4-Chloro-2-methyl-1,8-naphthyridine

4-Chloro-2-methyl-1,8-naphthyridine

C9H7ClN2 (178.0298)


   

4-Isothiocyanatobenzamide

4-Isothiocyanatobenzamide

C8H6N2OS (178.0201)


   

2-thiophen-2-yl-1H-pyrimidin-6-one

2-thiophen-2-yl-1H-pyrimidin-6-one

C8H6N2OS (178.0201)


   

2-(3-methoxy-3-oxopropyl)sulfanylacetic acid

2-(3-methoxy-3-oxopropyl)sulfanylacetic acid

C6H10O4S (178.03)


   

sodium 4-chloro-3,5-dimethylphenolate

sodium 4-chloro-3,5-dimethylphenolate

C8H8ClNaO (178.0161)


   

1-Chloro-5-isoquinolinamine

1-Chloro-5-isoquinolinamine

C9H7ClN2 (178.0298)


   

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

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

C8H6N2OS (178.0201)


   

3-chloroquinolin-8-amine

3-chloroquinolin-8-amine

C9H7ClN2 (178.0298)


   

4-chloro-6-methylquinazoline

4-chloro-6-methylquinazoline

C9H7ClN2 (178.0298)


   

1-Benzothiophen-2-ylboronic acid

1-Benzothiophen-2-ylboronic acid

C8H7BO2S (178.026)


D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D065093 - beta-Lactamase Inhibitors D004791 - Enzyme Inhibitors

   

4,6-Dihydroxy-2H-1-benzopyran-2-one

4,6-Dihydroxy-2H-1-benzopyran-2-one

C9H6O4 (178.0266)


   

1H-indene-2-carbonyl chloride

1H-indene-2-carbonyl chloride

C10H7ClO (178.0185)


   

8-Chloro-5-quinolinamine

8-Chloro-5-quinolinamine

C9H7ClN2 (178.0298)


   

5-CHLORO-2-PHENYL-3H-IMIDAZOLE

5-CHLORO-2-PHENYL-3H-IMIDAZOLE

C9H7ClN2 (178.0298)


   

2-chloro-5-methyl-1,6-naphthyridine

2-chloro-5-methyl-1,6-naphthyridine

C9H7ClN2 (178.0298)


   

5-Chloro-2-methyl-1,8-naphthyridine

5-Chloro-2-methyl-1,8-naphthyridine

C9H7ClN2 (178.0298)


   

3-(3-Chlorophenyl)-1H-pyrazole

3-(3-Chlorophenyl)-1H-pyrazole

C9H7ClN2 (178.0298)


   

7-chloroisoquinolin-3-amine

7-chloroisoquinolin-3-amine

C9H7ClN2 (178.0298)


   

4-Chloro-3-quinolinamine

4-Chloro-3-quinolinamine

C9H7ClN2 (178.0298)


   

2-chloro-8-methylquinazoline

2-chloro-8-methylquinazoline

C9H7ClN2 (178.0298)


   

4-Chloro-7-methylquinazoline

4-Chloro-7-methylquinazoline

C9H7ClN2 (178.0298)


   

O,Oμ-Diaminopropane-1,3-diol dihydrochloride

O,Oμ-Diaminopropane-1,3-diol dihydrochloride

C3H12Cl2N2O2 (178.0276)


   

2-Chloro-3-methylquinoxaline

2-Chloro-3-methylquinoxaline

C9H7ClN2 (178.0298)


   

1-Benzothien-7-ylboronicacid

1-Benzothien-7-ylboronicacid

C8H7BO2S (178.026)


   

Benzo[d]thiazole-5-carboxamide

Benzo[d]thiazole-5-carboxamide

C8H6N2OS (178.0201)


   

1-(6-Chloropyridin-3-yl)cyclopropanecarbonitrile

1-(6-Chloropyridin-3-yl)cyclopropanecarbonitrile

C9H7ClN2 (178.0298)


   

2-Oxo-2,3-dihydrobenzofuran-4-carboxylic acid

2-Oxo-2,3-dihydrobenzofuran-4-carboxylic acid

C9H6O4 (178.0266)


   

1H-Indene-1-carbonyl chloride (9CI)

1H-Indene-1-carbonyl chloride (9CI)

C10H7ClO (178.0185)


   

Tetrahydro-2H-thiopyran-4-carboxylic acid-1,1-dioxide

Tetrahydro-2H-thiopyran-4-carboxylic acid-1,1-dioxide

C6H10O4S (178.03)


   

3-Cyano-2-(methylthio)pyridine-6-carboxaldehyde

3-Cyano-2-(methylthio)pyridine-6-carboxaldehyde

C8H6N2OS (178.0201)


   

5-thiophen-2-yl-1h-pyrazin-2-one

5-thiophen-2-yl-1h-pyrazin-2-one

C8H6N2OS (178.0201)


   

1H-Imidazole,2-(4-chlorophenyl)-

1H-Imidazole,2-(4-chlorophenyl)-

C9H7ClN2 (178.0298)


   

4-Chloro-1-phenylpyrazole

4-Chloro-1-phenylpyrazole

C9H7ClN2 (178.0298)


   

2-AMINO-5-(4-PYRIDINYL)-1,3,4-THIADIAZO

2-AMINO-5-(4-PYRIDINYL)-1,3,4-THIADIAZO

C7H6N4S (178.0313)


   

8-chloroquinolin-2-amine

8-chloroquinolin-2-amine

C9H7ClN2 (178.0298)


   

6-Methoxy-1-benzofuran-2,3-dione

6-Methoxy-1-benzofuran-2,3-dione

C9H6O4 (178.0266)


   

4-Chloro-6-quinolinamine

4-Chloro-6-quinolinamine

C9H7ClN2 (178.0298)


   

2-chloro-3-pyrrol-1-ylpyridine

2-chloro-3-pyrrol-1-ylpyridine

C9H7ClN2 (178.0298)


   

4-CPI

4-(4-Chlorophenyl)-1H-imidazole

C9H7ClN2 (178.0298)


   

5-Amino-1,3-benzothiazole-2-carbaldehyde

5-Amino-1,3-benzothiazole-2-carbaldehyde

C8H6N2OS (178.0201)


   

6-Chloro-4-methylquinazoline

6-Chloro-4-methylquinazoline

C9H7ClN2 (178.0298)


   

3-Chloroisoquinolin-4-amine

3-Chloroisoquinolin-4-amine

C9H7ClN2 (178.0298)


   

5-CHLOROISOQUINOLIN-8-AMINE

5-CHLOROISOQUINOLIN-8-AMINE

C9H7ClN2 (178.0298)


   

4-(1,2,3-Thiadiazol-4-yl)phenol

4-(1,2,3-Thiadiazol-4-yl)phenol

C8H6N2OS (178.0201)


   

benzo[d]isothiazole-3-carboxamide

benzo[d]isothiazole-3-carboxamide

C8H6N2OS (178.0201)


   

5-(4-pyridyl)-1h-1,2,4-triazole-3-thiol

5-(4-pyridyl)-1h-1,2,4-triazole-3-thiol

C7H6N4S (178.0313)


   

4-(4-chlorophenyl)but-3-yn-2-one

4-(4-chlorophenyl)but-3-yn-2-one

C10H7ClO (178.0185)


   

2-Chloro-7-methylquinoxaline

2-Chloro-7-methylquinoxaline

C9H7ClN2 (178.0298)


   

2-(4-Fluorophenyl)thiophene

2-(4-Fluorophenyl)thiophene

C10H7FS (178.0252)


   

6-HYDROXYBENZOFURAN-2-CARBOXYLIC ACID

6-HYDROXYBENZOFURAN-2-CARBOXYLIC ACID

C9H6O4 (178.0266)


   

3-(4-Pyridinyl)-5-amino-[1,2,4]thiadiazole

3-(4-Pyridinyl)-5-amino-[1,2,4]thiadiazole

C7H6N4S (178.0313)


   

1H-Indene-3-carbonyl chloride (9CI)

1H-Indene-3-carbonyl chloride (9CI)

C10H7ClO (178.0185)


   

2-(4-PYRIDINYL)-4(5H)-THIAZOLONE

2-(4-PYRIDINYL)-4(5H)-THIAZOLONE

C8H6N2OS (178.0201)


   

2,5-Diamino-4,6-dihydroxypyrimidine hydrochloride

2,5-Diamino-4,6-dihydroxypyrimidine hydrochloride

C4H7ClN4O2 (178.0258)


   

Quinoxaline, 2-chloro-5-methyl- (9CI)

Quinoxaline, 2-chloro-5-methyl- (9CI)

C9H7ClN2 (178.0298)


   

3-chloroquinolin-2-amine

3-chloroquinolin-2-amine

C9H7ClN2 (178.0298)


   

8-Chloro-6-quinolinamine

8-Chloro-6-quinolinamine

C9H7ClN2 (178.0298)


   

2-(Trifluoromethoxy)phenol

2-(Trifluoromethoxy)phenol

C7H5F3O2 (178.0242)


   

p-Trifluoromethoxy phenol

p-Trifluoromethoxy phenol

C7H5F3O2 (178.0242)


   

6-Chloro-8-quinolinamine

6-Chloro-8-quinolinamine

C9H7ClN2 (178.0298)


   

1-Chloro-2-naphthol

1-Chloro-2-naphthol

C10H7ClO (178.0185)


   

2-(1,1-Dioxidotetrahydrothiophen-3-yl)acetic acid

2-(1,1-Dioxidotetrahydrothiophen-3-yl)acetic acid

C6H10O4S (178.03)


   

2-(4-METHYLTHIAZOL-5-YL)ETHANAMINE HYDROCHLORIDE

2-(4-METHYLTHIAZOL-5-YL)ETHANAMINE HYDROCHLORIDE

C6H11ClN2S (178.0331)


   

2-Chloro-4-methylquinazoline

2-Chloro-4-methylquinazoline

C9H7ClN2 (178.0298)


   

Thieno[3,2-c]pyridine-3-carboxamide (9CI)

Thieno[3,2-c]pyridine-3-carboxamide (9CI)

C8H6N2OS (178.0201)


   

Boric acid disodium salt,tetrahydrate

Boric acid disodium salt,tetrahydrate

BH9Na2O7 (178.0237)


   

3-(2-CHLORO-PHENYL)-1H-PYRAZOLE

3-(2-CHLORO-PHENYL)-1H-PYRAZOLE

C9H7ClN2 (178.0298)


   

BROMOBIS(DIMETHYLAMINO)BORANE

BROMOBIS(DIMETHYLAMINO)BORANE

C4H12BBrN2 (178.0277)


   

8-Chloro-2-methyl-1,7-naphthyridine

8-Chloro-2-methyl-1,7-naphthyridine

C9H7ClN2 (178.0298)


   

7-CHLOROQUINOLIN-8-AMINE

7-CHLOROQUINOLIN-8-AMINE

C9H7ClN2 (178.0298)


   

6-Chloro-7-quinolinamine

6-Chloro-7-quinolinamine

C9H7ClN2 (178.0298)


   

4-CHLORO-8-METHYLQUINAZOLINE

4-CHLORO-8-METHYLQUINAZOLINE

C9H7ClN2 (178.0298)


   

4-chloro-2-methyl-1,5-naphthyridine

4-chloro-2-methyl-1,5-naphthyridine

C9H7ClN2 (178.0298)


   

5-Methoxy-2-benzofuran-1,3-dione

5-Methoxy-2-benzofuran-1,3-dione

C9H6O4 (178.0266)


   

5,6-DIAMINOPYRIMIDINE-2,4(1H,3H)-DIONE

5,6-DIAMINOPYRIMIDINE-2,4(1H,3H)-DIONE

C4H7ClN4O2 (178.0258)


   

2-mercapto-4(3h)-quinazolinone

2-mercapto-4(3h)-quinazolinone

C8H6N2OS (178.0201)


   

6-Chloro-7-methylquinoxaline

6-Chloro-7-methylquinoxaline

C9H7ClN2 (178.0298)


   

4-(THIAZOL-2-YL)PYRIMIDIN-2-AMINE

4-(THIAZOL-2-YL)PYRIMIDIN-2-AMINE

C7H6N4S (178.0313)


   

3-Chloroisoquinolin-5-amine

3-Chloroisoquinolin-5-amine

C9H7ClN2 (178.0298)


   

2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE

2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE

C9H6O4 (178.0266)


   

2-Benzothiazolecarboxamide(6CI,8CI,9CI)

2-Benzothiazolecarboxamide(6CI,8CI,9CI)

C8H6N2OS (178.0201)


   

1,2,3,4-Thiatriazol-5-amine,N-phenyl-

1,2,3,4-Thiatriazol-5-amine,N-phenyl-

C7H6N4S (178.0313)


   

8-CHLORO-2-NAPHTHALENOL

8-CHLORO-2-NAPHTHALENOL

C10H7ClO (178.0185)


   

4-Chloro-7-quinolinamine

4-Chloro-7-quinolinamine

C9H7ClN2 (178.0298)


   

4-Chloroquinolin-8-amine

4-Chloroquinolin-8-amine

C9H7ClN2 (178.0298)


   

Quinoxaline, 2-chloro-8-methyl- (9CI)

Quinoxaline, 2-chloro-8-methyl- (9CI)

C9H7ClN2 (178.0298)


   

6-chloroisoquinolin-1-amine

6-chloroisoquinolin-1-amine

C9H7ClN2 (178.0298)


   

1,2,4,5-TETRACYANOBENZENE

1,2,4,5-TETRACYANOBENZENE

C10H2N4 (178.0279)


   

5-Carboxyphthalide

5-Carboxyphthalide

C9H6O4 (178.0266)


   

3-(4-chlorophenyl)pyrazole

3-(4-chlorophenyl)pyrazole

C9H7ClN2 (178.0298)


   

5-Chloro-8-quinolinamine

5-Chloro-8-quinolinamine

C9H7ClN2 (178.0298)


   

4-chloro-2-methylquinazoline

4-chloro-2-methylquinazoline

C9H7ClN2 (178.0298)


   

1-(2-chlorophenyl)imidazole

1-(2-chlorophenyl)imidazole

C9H7ClN2 (178.0298)


   

5-Amino-6-chloroquinoline

5-Amino-6-chloroquinoline

C9H7ClN2 (178.0298)


   

1,2-dihydro-5-(3-pyridinyl)-3h-1,2,4-triazole-3-thione

1,2-dihydro-5-(3-pyridinyl)-3h-1,2,4-triazole-3-thione

C7H6N4S (178.0313)


   

5-Isoquinolinamine,7-chloro-(9CI)

5-Isoquinolinamine,7-chloro-(9CI)

C9H7ClN2 (178.0298)


   

Potassium(N-propylsulfamoyl)amide

Potassium(N-propylsulfamoyl)amide

C3H11N2O2S.K (178.0178)


   

3-chloroquinolin-6-amine

3-chloroquinolin-6-amine

C9H7ClN2 (178.0298)


   

1-chloro-4-methylphthalazine

1-chloro-4-methylphthalazine

C9H7ClN2 (178.0298)


   

4-AMINO-8-CHLOROQUINOLINE

4-AMINO-8-CHLOROQUINOLINE

C9H7ClN2 (178.0298)


   

5-phenyl-1,3,4-thiadiazol-2(3H)-one

5-phenyl-1,3,4-thiadiazol-2(3H)-one

C8H6N2OS (178.0201)


   

4-amino-6-chloroquinoline

4-amino-6-chloroquinoline

C9H7ClN2 (178.0298)


   

4-(Pyrazin-2-yl)thiazol-2-amine

4-(Pyrazin-2-yl)thiazol-2-amine

C7H6N4S (178.0313)


   

6-chloroquinolin-2-amine

6-chloroquinolin-2-amine

C9H7ClN2 (178.0298)


   

1 3-DIAMINOACETONE DIHYDROCHLORIDE

1 3-DIAMINOACETONE DIHYDROCHLORIDE

C3H12Cl2N2O2 (178.0276)


   

4-Chloro-3-nitroanisole

4-Chloro-3-nitroanisole

C7H6F3P (178.0159)


   

6-(2-THIENYL)-3(2H)-PYRIDAZINONE

6-(2-THIENYL)-3(2H)-PYRIDAZINONE

C8H6N2OS (178.0201)


   

2-Chloro-6-hydroxynaphthalene

2-Chloro-6-hydroxynaphthalene

C10H7ClO (178.0185)


   

4-amino-6-chloroquinoline hydrochloride

4-amino-6-chloroquinoline hydrochloride

C9H7ClN2 (178.0298)


   

3-(Trifluoromethoxy)phenol

3-(Trifluoromethoxy)phenol

C7H5F3O2 (178.0242)


   

bay1251152

bay1251152

C6H10O4S (178.03)


   

5-HYDROXYBENZOFURAN-2-CARBOXYLIC ACID

5-HYDROXYBENZOFURAN-2-CARBOXYLIC ACID

C9H6O4 (178.0266)


   

7-Chloroquinolin-3-amine

7-Chloroquinolin-3-amine

C9H7ClN2 (178.0298)


   

5-Isoxazoleacetic acid, alpha-amino-3-chloro-4,5-dihydro-

5-Isoxazoleacetic acid, alpha-amino-3-chloro-4,5-dihydro-

C5H7ClN2O3 (178.0145)


D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

3-Chloro-1-phenyl-1H-pyrazole

3-Chloro-1-phenyl-1H-pyrazole

C9H7ClN2 (178.0298)


   

5-Chloro-1-phenyl-1H-pyrazole

5-Chloro-1-phenyl-1H-pyrazole

C9H7ClN2 (178.0298)


   

Daphnetol

InChI=1/C9H6O4/c10-6-3-1-5-2-4-7(11)13-9(5)8(6)12/h1-4,10,12

C9H6O4 (178.0266)


7,8-dihydroxycoumarin is a hydroxycoumarin. Daphnetin is a natural product found in Euphorbia dracunculoides, Rhododendron lepidotum, and other organisms with data available. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4]. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1?, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research[1][2][3][4].

   

31721-94-5

4H-1-Benzopyran-4-one, 5,7-dihydroxy-

C9H6O4 (178.0266)


5,7-Dihydroxychromone, the extract of Cudrania tricuspidata, activates Nrf2/ARE signal and exerts neuroprotective effects against 6-hydroxydopamine (6-OHDA)-induced oxidative stress and apoptosis. 5,7-Dihydroxychromone inhibits the expression of activated caspase-3 and caspase-9 and cleaved PARP in 6-OHDA-induced SH-SY5Y cells[1]. 5,7-Dihydroxychromone, the extract of Cudrania tricuspidata, activates Nrf2/ARE signal and exerts neuroprotective effects against 6-hydroxydopamine (6-OHDA)-induced oxidative stress and apoptosis. 5,7-Dihydroxychromone inhibits the expression of activated caspase-3 and caspase-9 and cleaved PARP in 6-OHDA-induced SH-SY5Y cells[1].

   

FR-0256

5H-Tetrazole-5-thione, 1,2-dihydro-1-phenyl-

C7H6N4S (178.0313)


   

2732-18-5

InChI=1\C9H6O4\c10-5-3-7(11)6-1-2-9(12)13-8(6)4-5\h1-4,10-11

C9H6O4 (178.0266)


5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2]. 5,7-Dihydroxycoumarin is a coumarin isolated from the inflorescences of Macaranga triloba. 5,7-Dihydroxycoumarin has antibacterial activities[1][2].

   

6-Hydroxy-2,3-dihydro-1,3-benzothiazole-2-carbonitrile

6-Hydroxy-2,3-dihydro-1,3-benzothiazole-2-carbonitrile

C8H6N2OS (178.0201)


   

2-Azaniumyl-2-(3-chloro-4,5-dihydro-1,2-oxazol-5-yl)acetate

2-Azaniumyl-2-(3-chloro-4,5-dihydro-1,2-oxazol-5-yl)acetate

C5H7ClN2O3 (178.0145)


   

S-carboxylatomethyl-L-cysteine(1-)

S-carboxylatomethyl-L-cysteine(1-)

C5H8NO4S- (178.0174)


The conjugate base of S-carboxymethyl-L-cysteine having anionic carboxy groups and a protonated amino group; major species at pH 7.3.

   

S-carboxymethyl-D-cysteine

S-carboxymethyl-D-cysteine

C5H8NO4S- (178.0174)


   

Benzylmalonate

Benzylmalonate

C9H6O4-2 (178.0266)


   

(Z)-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)prop-2-enoic acid

(Z)-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)prop-2-enoic acid

C9H6O4 (178.0266)


   

[Ti(eta(5)-C5H5)2]

[Ti(eta(5)-C5H5)2]

C10H10Ti-6 (178.0262)


   

3-Methylthioaspartate(1-)

3-Methylthioaspartate(1-)

C5H8NO4S- (178.0174)


An alpha-amino-acid anion obtained by deprotonation of the two carboxy groups and protonation of the amino group of 3-methylthioaspartic acid.

   

N-acetyl-S-hydroxy-L-cysteine

N-acetyl-S-hydroxy-L-cysteine

C5H8NO4S- (178.0174)


   

Dimethyl 2,2-thiobisacetate

Dimethyl 2,2-thiobisacetate

C6H10O4S (178.03)


   

Ninhydrin

Ninhydrin

C9H6O4 (178.0266)


A member of the class of indanones that is indane-1,3-dione bearing two additional hydroxy substituents at position 2. D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D011838 - Radiation-Sensitizing Agents

   

3,7-dihydroxychromen-2-one

3,7-dihydroxychromen-2-one

C9H6O4 (178.0266)


   

Dihydroxymethylthiopentenoic acid

Dihydroxymethylthiopentenoic acid

C6H10O4S (178.03)


   

Aminochloroquinoline

Aminochloroquinoline

C9H7ClN2 (178.0298)


   

5,8-dihydroxychromen-2-one

5,8-dihydroxychromen-2-one

C9H6O4 (178.0266)


   

3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

C9H6O4 (178.0266)


   

4,8-dihydroxychromen-2-one

4,8-dihydroxychromen-2-one

C9H6O4 (178.0266)