Search More · GCI-TPs

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

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

8 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

7 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

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Product

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Upstream Precursor

MVHYKTPDKPMBPP-UHFFFAOYSA-N

C1=CC=C2C(=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O)Cl

Environmental

Product

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Upstream Precursor

MVHYKTPDKPMBPP-UHFFFAOYSA-N

C1=CC=C2C(=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O)Cl

Abiotic

Product

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Upstream Precursor

MVHYKTPDKPMBPP-UHFFFAOYSA-N

C1=CC=C2C(=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O)Cl

Abiotic

Product

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Upstream Precursor

MVHYKTPDKPMBPP-UHFFFAOYSA-N

C1=CC=C2C(=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O)Cl

Environmental

Product

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Previewing top 5 entries. If you want the full results, please use the download button above.

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

C(=O)(C1=C(C=C2C=CC=CC2=C1)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Environmental

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

C(=O)(C1=C(C=C2C=CC=CC2=C1)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

C(=O)(C1=C(C=C2C=CC=CC2=C1)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Downstream Successor

JWAZRIHNYRIHIV-UHFFFAOYSA-N

2-Naphthol

C1=CC2=C(C=C1)C=C(C=C2)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Environmental

Downstream Successor

JWAZRIHNYRIHIV-UHFFFAOYSA-N

2-Naphthol

C1=CC2=C(C=C1)C=C(C=C2)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Environmental

Downstream Successor

BMHCSEJDJONPSF-UHFFFAOYSA-N

3,4-Dihydroxynaphthalene-2-carboxylic acid

C1(=C(C(=CC2=CC=CC=C21)C(=O)O)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Downstream Successor

BMHCSEJDJONPSF-UHFFFAOYSA-N

3,4-Dihydroxynaphthalene-2-carboxylic acid

C1(=C(C(=CC2=CC=CC=C21)C(=O)O)O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Abiotic

Downstream Successor

JRNGUTKWMSBIBF-UHFFFAOYSA-N

2,3-Dihydroxynaphthalene

C1(=CC2=CC=CC=C2C=C1O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Environmental

Downstream Successor

JRNGUTKWMSBIBF-UHFFFAOYSA-N

2,3-Dihydroxynaphthalene

C1(=CC2=CC=CC=C2C=C1O)O

Precursor

JNDPAMPDNGVEPY-UHFFFAOYSA-N

3-Hydroxy-N-1H-indazol-6-ylnaphthalene-2-carboxamide

C1=CC=C2C=C(C(=CC2=C1)C(=O)NC3=CC4=C(C=C3)C=NN4)O

Environmental

Downstream Successor

FGPKSIXNTNDIJT-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4-chloro-3-hydroxy-

C1=CC=CC2=CC(=C(C(=C21)Cl)O)C(=O)O

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

No Original Precursors

No entries were found for this section with the current query and depth.

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