require_once( "../navigation.include" ); ?>
check_image( "../cid_images/cid_469.png" ); ?>
check_image( "../cid_thumbs/cid_440579.png" ); ?>
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check_image( "../cid_thumbs/cid_2803011.png" ); ?>
check_image( "../cid_thumbs/cid_1412213.png" ); ?>
check_image( "../cid_thumbs/cid_6746824.png" ); ?>
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check_image( "../cid_thumbs/cid_5341934.png" ); ?>
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check_image( "../cid_thumbs/cid_325576.png" ); ?>
check_image( "../cid_thumbs/cid_6794970.png" ); ?>
check_image( "../cid_thumbs/cid_1027474.png" ); ?>
check_image( "../cid_thumbs/cid_2808142.png" ); ?>
check_image( "../cid_thumbs/cid_1462739.png" ); ?>
check_image( "../cid_thumbs/cid_4120351.png" ); ?>
check_image( "../cid_thumbs/cid_4490359.png" ); ?>
check_image( "../cid_thumbs/cid_6291813.png" ); ?>
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2-Aminoadipic Acid A metabolite in the principal biochemical pathway of lysine. It antagonizes neuroexcitatory activity modulated by the glutamate receptor, N-METHYL-D-ASPARTATE; (NMDA).
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pre_formula( "InChI=1/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/f/h8,10H", "jqp073/469.html" ); ?>
Molecular Formula:
C6H11NO4
InChI: InChI=1/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/f/h8,10H
InChIKey: InChIKey=OYIFNHCXNCRBQI-PSPNOWEWCJ
SMILES: NC(CCCC(O)=O)C(O)=O
CAS number 542-32-5
Names:
AMINOADIPIC ACID, ALPHA
Hexanedioic acid, 2-amino-
NSC46994
α-aminoadipic acid
.alpha.-Aminoadipate
.alpha.-Aminoadipic acid
2-Aminoadipate
2-AMINOADIPIC ACID
2-aminoadipic acid
2-aminohexanedioic acid
542-32-5
name_it( "InChI=1/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/f/h8,10H", "jqp073/469.html" ); ?>
Registries:
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PubChem CID 469
Beilstein =1724349
Beilstein =1773077
CAS 542-32-5 (from NIST)
ChEBI 37024
PubChem ID 100205
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