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Depiction
Upstream Precursor
[(2R,3S,4R,5R)-5-[6-(6-aminohexylamino)purin-9-yl]-4-hydroxy-2-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate
C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)…
Environmental
Depiction
Product
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
Adenine
NC1=C2C(=NC=N1)NC=N2
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
Gamma-Aminobutyric Acid
C(CCCN)(O)=O
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
OC1C(OC(C1O)N2C=NC3=C(N=CN=C32)N)CO
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
6-Aminohexanoic Acid
NCCCCCC(=O)O
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Abiotic
Depiction
Downstream Successor
(5-(6-Aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl)methyl dihydrogen phosphate
OC1C(OC(C1O)N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
(5-(6-Aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl)methyl dihydrogen phosphate
OC1C(OC(C1O)N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
6-Hydroxyaminopurine
C1=NC(=C2C(=N1)NC=N2)NO
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
D-lyxono-1,4-lactone
C([C@@H]1[C@@H]([C@@H](C(=O)O1)O)O)O
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
6-Aminohexanal
O=CCCCCCN
Depiction
Precursor
{[(2R,3S,4R,5R)-5-{6-[(6-aminohexyl)amino]-9H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)NCCCCCCN
Environmental
Depiction
Downstream Successor
6-Aminohexanal
O=CCCCCCN
No Original Precursors

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No Dead-Ends

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