NCBI Taxonomy: 260499

Asparagopsis taxiformis (ncbi_taxid: 260499)

found 36 associated metabolites at species taxonomy rank level.

Ancestor: Asparagopsis

Child Taxonomies: none taxonomy data.

Dichloroacetate

2,2-dichloroacetic acid

C2H2Cl2O2 (127.9432)


An organochlorine compound comprising acetic acid carrying two chloro substituents at the 2-position. It occurs in nature in seaweed, Asparagopsis taxiformis. KEIO_ID D160 KEIO_ID D034

   

Iodoform

Carbon triiodide

CHI3 (393.7213)


D - Dermatologicals > D09 - Medicated dressings > D09A - Medicated dressings > D09AA - Medicated dressings with antiinfectives C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent Same as: D01910

   

Dibromochloromethane

Dibromo-chloro-methane

CHBr2Cl (205.8133)


Dibromochloromethane belongs to the family of Organochlorides. These are organic compounds containing a chlorine atom

   

Bromoform

Methyl tribromide

CHBr3 (249.7628)


Bromoform, also known as Tribromomethane or Methyl tribromide, is classified as a member of the Trihalomethanes. Trihalomethanes are organic compounds in which exactly three of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms. Trace amounts of 1,2-dibromoethane occur naturally in the ocean, where it is formed probably by algae and kelp. Bromoform is formally rated as an unfounded non-carcinogenic (IARC 3) potentially toxic compound. Exposure to bromoform may occur from the consumption of chlorinated drinking water. The acute (short-term) effects from inhalation or ingestion of high levels of bromoform in humans and animals consist of nervous system effects such as the slowing down of brain functions, and injury to the liver and kidney. Chronic (long-term) animal studies indicate effects on the liver, kidney, and central nervous system (CNS) from oral exposure to bromoform. Human data are considered inadequate in providing evidence of cancer by exposure to bromoform, while animal data indicate that long-term oral exposure can cause liver and intestinal tumors. Bromoform has been classified as a Group B2, probable human carcinogen. Most of the bromoform that enters the environment is formed as disinfection byproducts known as the trihalomethanes when chlorine is added to drinking water or swimming pools to kill bacteria. In the past, it was used as a solvent, sedative and flame retardant, but now it is mainly used as a laboratory reagent. Bromine is a halogen element with the symbol Br and atomic number 35. Diatomic bromine does not occur naturally, but bromine salts can be found in crustal rock. Bromoform is a pale yellow liquid at room temperature, with a high refractive index, very high density, and sweet odor is similar to that of chloroform. D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D013723 - Teratogens

   

DIBROMOACETIC ACID

2,2-dibromoacetic acid

C2H2Br2O2 (215.8422)


A monocarboxylic acid that is acetic acid in which two of the methyl hydrogens are replaced by bromo groups. D009676 - Noxae > D000477 - Alkylating Agents

   

DIBROMOIODOMETHANE

DIBROMOIODOMETHANE

CHBr2I (297.749)


   

1-Bromoacetone

1-Bromoacetone

C3H5BrO (135.9524)


   

Diiodoacetic acid

Diiodoethanoic acid

C2H2I2O2 (311.8144)


   

Ethyl 2-Bromo-2-iodoacetate

Ethyl 2-Bromo-2-iodoethanoate

C4H6BrIO2 (291.8596)


   

3,4-Dibromobut-3-en-2-one

3,4-Dibromobut-3-en-2-one

C4H4Br2O (225.8629)


   

DICHLOROACETIC ACID

DICHLOROACETIC ACID

C2H2Cl2O2 (127.9432)


   

Tetrabromomethane

Tetrabromomethane

CBr4 (327.6733)


   

2,2-dichloroacetic acid

2,2-dichloroacetic acid

C2H2Cl2O2 (127.9432)


   

IODOFORM

IODOFORM

CHI3 (393.7213)


D - Dermatologicals > D09 - Medicated dressings > D09A - Medicated dressings > D09AA - Medicated dressings with antiinfectives C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent

   

Bromoform

tribromomethane

CHBr3 (249.7628)


D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D013723 - Teratogens

   

DIBROMOCHLOROMETHANE

DIBROMOCHLOROMETHANE

CHBr2Cl (205.8133)


   

(3s)-1,1,3-tribromo-3-chloroprop-1-ene

(3s)-1,1,3-tribromo-3-chloroprop-1-ene

C3H2Br3Cl (309.7395)


   

1,1,3,3,3-pentabromoprop-1-en-2-yl 2,2,2-tribromoacetate

1,1,3,3,3-pentabromoprop-1-en-2-yl 2,2,2-tribromoacetate

C5Br8O2 (723.3365)


   

3,4-dibromo-1-iodobut-3-en-2-one

3,4-dibromo-1-iodobut-3-en-2-one

C4H3Br2IO (351.7595)


   

1,3,3-tribromo-1-iodoprop-1-ene

1,3,3-tribromo-1-iodoprop-1-ene

C3H2Br3I (401.6751)


   

(2s)-1,1,4,4-tetrabromobut-3-en-2-ol

(2s)-1,1,4,4-tetrabromobut-3-en-2-ol

C4H4Br4O (383.6996)


   

(3z)-1,1,3,4-tetrabromobut-3-en-2-one

(3z)-1,1,3,4-tetrabromobut-3-en-2-one

C4H2Br4O (381.6839)


   

1,1,3,3,3-pentabromoprop-1-en-2-yl 2,2-dibromoacetate

1,1,3,3,3-pentabromoprop-1-en-2-yl 2,2-dibromoacetate

C5HBr7O2 (645.426)


   

bromo(iodo)acetic acid

bromo(iodo)acetic acid

C2H2BrIO2 (263.8283)


   

1,1,3,3-tetrabromoprop-1-ene

1,1,3,3-tetrabromoprop-1-ene

C3H2Br4 (353.689)


   

(3z)-3,4-dibromo-1-iodobut-3-en-2-one

(3z)-3,4-dibromo-1-iodobut-3-en-2-one

C4H3Br2IO (351.7595)


   

1,1,4,4-tetrabromobut-3-en-2-ol

1,1,4,4-tetrabromobut-3-en-2-ol

C4H4Br4O (383.6996)


   

(1e)-1,3,3-tribromo-1-iodoprop-1-ene

(1e)-1,3,3-tribromo-1-iodoprop-1-ene

C3H2Br3I (401.6751)


   

(3z)-3,4-dibromobut-3-en-2-one

(3z)-3,4-dibromobut-3-en-2-one

C4H4Br2O (225.8629)


   

1,1,3-tribromo-3-chloroprop-1-ene

1,1,3-tribromo-3-chloroprop-1-ene

C3H2Br3Cl (309.7395)


   

(3z)-1,3,4-tribromobut-3-en-2-one

(3z)-1,3,4-tribromobut-3-en-2-one

C4H3Br3O (303.7734)


   

1,1,3,4-tetrabromobut-3-en-2-one

1,1,3,4-tetrabromobut-3-en-2-one

C4H2Br4O (381.6839)


   

1,1-dibromo-3,3-dichloroprop-1-ene

1,1-dibromo-3,3-dichloroprop-1-ene

C3H2Br2Cl2 (265.79)


   

ethyl (2r)-2-bromo-2-iodoacetate

ethyl (2r)-2-bromo-2-iodoacetate

C4H6BrIO2 (291.8596)


   

1,3,4-tribromobut-3-en-2-one

1,3,4-tribromobut-3-en-2-one

C4H3Br3O (303.7734)


   

(r)-bromo(iodo)acetic acid

(r)-bromo(iodo)acetic acid

C2H2BrIO2 (263.8283)