2-Aminophenol is an organic compound with the formula C6H7NO. Along with its isomer 4-aminophenol, it is an amphoteric molecule and a reducing agent. It is a useful reagent for the synthesis of dyes and heterocyclic compounds. Reflecting its slight hydrophilic character, white powder is moderately soluble in alcohols and can be recrystallized from hot water. |
Read full article at Wikipedia
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InChI=1S/C21H31N3O5S/c1- 14(2) 11- 17(23- 19(26) 16(22- 13- 25) 9- 10- 30- 3) 20(27) 24- 18(21(28) 29) 12- 15- 7- 5- 4- 6- 8- 15/h4- 8,13- 14,16- 18H,9- 12H2,1- 3H3,(H,22,25) (H,23,26) (H,24,27) (H,28,29) /t16- ,17- ,18- /m0/s1 |
PRQROPMIIGLWRP-BZSNNMDCSA-N |
[H]C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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View more via ChEBI Ontology
Outgoing
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N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
has functional parent
N-formyl-L-methionine
(CHEBI:16552)
N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
has functional parent
L-leucine
(CHEBI:15603)
N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
has functional parent
L-phenylalanine
(CHEBI:17295)
N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
is a
tripeptide
(CHEBI:47923)
N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
is conjugate acid of
N-formyl-L-methionyl-L-leucyl-L-phenylalaninate
(CHEBI:194314)
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Incoming
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N-formyl-L-methionyl-L-leucyl-L-phenylalaninate
(CHEBI:194314)
is conjugate base of
N-formyl-L-methionyl-L-leucyl-L-phenylalanine
(CHEBI:53490)
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N-formyl-L-methionyl-L-leucyl-L-phenylalanine
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F-Met-Leu-Phe
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ChemIDplus
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fMetLeuPhe
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SUBMITTER
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fMLF
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SUBMITTER
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fMLP
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SUBMITTER
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N-formyl-L-Met-L-Leu-L-Phe
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ChEBI
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N-formyl-L-methionyl-L-leucyl-L-phenylalanine
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KEGG COMPOUND
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N-formyl-Met-Leu-Phe
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SUBMITTER
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N-formyl-Met-Leu-Phe-OH
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ChEBI
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N-formyl-methionyl-leucyl-phenylalanine
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ChemIDplus
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N-formylmethionine leucyl-phenylalanine
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ChemIDplus
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2315783
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Beilstein Registry Number
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Beilstein
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59880-97-6
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CAS Registry Number
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KEGG COMPOUND
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59880-97-6
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CAS Registry Number
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ChemIDplus
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8023425
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Beilstein Registry Number
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Beilstein
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16236365
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PubMed citation
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Europe PMC
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17907740
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18092743
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19067145
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19069235
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21126546
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22484311
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23002436
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