Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

4 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

Previewing top 10 entries. If you want the full results, please use the download button above.

Upstream Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Product

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Upstream Precursor

NAFTTZRWODATMK-UHFFFAOYSA-N

CC(C)COC(=O)NC1=CC=CC2=C1C(=CC(=C2O)C(=O)OC3=CC=CC=C3)Cl

Abiotic

Product

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

PriorBiotransformation

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

TXXHDPDFNKHHGW-UHFFFAOYSA-N

2,4-Hexadienedioic acid, (2Z,4Z)-

C(C=CC=CC(=O)O)(O)=O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

PriorBiotransformation

Downstream Successor

TXXHDPDFNKHHGW-UHFFFAOYSA-N

2,4-Hexadienedioic acid, (2Z,4Z)-

C(C=CC=CC(=O)O)(O)=O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

PriorBiotransformation

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

ZXEKIIBDNHEJCQ-UHFFFAOYSA-N

Isobutanol

OCC(C)C

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

PriorBiotransformation

Downstream Successor

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Hydroquinone

C1(=CC=C(C=C1)O)O

Precursor

AVXGZOSFTCLSHE-UHFFFAOYSA-N

Phenyl 1-hydroxy-5-{[(2-methylpropoxy)carbonyl]amino}naphthalene-2-carboxylate

CC(C)COC(=O)NC1=CC=CC2=C1C=CC(=C2O)C(=O)OC3=CC=CC=C3

Abiotic

Downstream Successor

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Hydroquinone

C1(=CC=C(C=C1)O)O

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

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