Search More · GCI-TPs

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

12 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

17 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

17 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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

Upstream Precursor

ORJDDOBAOGKRJV-UHFFFAOYSA-N

Npc235117

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

ORJDDOBAOGKRJV-UHFFFAOYSA-N

Npc235117

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

AXILYAWWFKTKLH-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)Cl)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

AXILYAWWFKTKLH-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)Cl)O

Environmental

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

AXILYAWWFKTKLH-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)Cl)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

AXILYAWWFKTKLH-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)Cl)O

Environmental

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

HUMXSJOWZZQBLF-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1Cl)C3=CC=C(C=C3)O)O

Abiotic

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

HUMXSJOWZZQBLF-UHFFFAOYSA-N

COC1=CC(=C2C(=O)CC(OC2=C1Cl)C3=CC=C(C=C3)O)O

Environmental

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Upstream Precursor

PPHVVYSAHIBOED-UHFFFAOYSA-N

COC1=C(C(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)Cl

Environmental

Product

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Downstream Successor

SBHXYTNGIZCORC-UHFFFAOYSA-N

(+-)-Eriodictyol

C1(=CC=C(C=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Environmental

Downstream Successor

SBHXYTNGIZCORC-UHFFFAOYSA-N

(+-)-Eriodictyol

C1(=CC=C(C=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Environmental

Downstream Successor

UUTCBZYCHDMQQB-UHFFFAOYSA-N

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

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Abiotic

Downstream Successor

FKFCDSSCQGQEQH-UHFFFAOYSA-N

C1C(OC2=CC(=CC(=C2C1=O)O)O)C(C=CC(O)=O)=CC(O)=O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Environmental

Downstream Successor

FKFCDSSCQGQEQH-UHFFFAOYSA-N

C1C(OC2=CC(=CC(=C2C1=O)O)O)C(C=CC(O)=O)=CC(O)=O

Precursor

DJOJDHGQRNZXQQ-UHFFFAOYSA-N

4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O

Environmental

Downstream Successor

FTVWIRXFELQLPI-UHFFFAOYSA-N

(+-)-Naringenin

C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)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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