Search More · GCI-TPs

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=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

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

YQMYCLQUUAANHT-UHFFFAOYSA-N

2H-Isoindole-2-acetic acid, 1,3-dihydro-alpha-(3-((4-nitrophenyl)amino)-3-oxopropyl)-1,3-dioxo-

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC3=CC=C(C=C3)[N+](=O)[O-]…

Abiotic

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

YQMYCLQUUAANHT-UHFFFAOYSA-N

2H-Isoindole-2-acetic acid, 1,3-dihydro-alpha-(3-((4-nitrophenyl)amino)-3-oxopropyl)-1,3-dioxo-

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC3=CC=C(C=C3)[N+](=O)[O-]…

Environmental

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

IJJWGHLNXVQFMC-UHFFFAOYSA-N

OC(=O)CCC(C(=O)O)[N+]1(C(=O)C2=CC=CC=C2C1=O)[O-]

Environmental

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

UEJJHQNACJXSKW-UHFFFAOYSA-O

2-(2,6-Dioxopiperidin-1-ium-3-yl)isoindole-1,3-dione

C1CC(=O)NC(=O)C1[NH+]2C(=O)C3=CC=CC=C3C2=O

Abiotic

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

UEJJHQNACJXSKW-UHFFFAOYSA-O

2-(2,6-Dioxopiperidin-1-ium-3-yl)isoindole-1,3-dione

C1CC(=O)NC(=O)C1[NH+]2C(=O)C3=CC=CC=C3C2=O

Environmental

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

MDHUPZOTZZFNKJ-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC(C=CC(=O)O)=CC(O)=O)C(=O)O

Environmental

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

MDHUPZOTZZFNKJ-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC(C=CC(=O)O)=CC(O)=O)C(=O)O

Abiotic

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

QRDNQJNKUVNKQC-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC3=CC=C(C(=C3)O)O)C(=O)O

Abiotic

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Upstream Precursor

QRDNQJNKUVNKQC-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)NC3=CC=C(C(=C3)O)O)C(=O)O

Environmental

Product

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Downstream Successor

XKJCHHZQLQNZHY-UHFFFAOYSA-N

Phthalimide

N1C(=O)c2ccccc2C1=O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Environmental

Downstream Successor

XKJCHHZQLQNZHY-UHFFFAOYSA-N

Phthalimide

N1C(=O)c2ccccc2C1=O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Environmental

Downstream Successor

HWXBTNAVRSUOJR-UHFFFAOYSA-N

(+-)-2-Hydroxyglutaric acid

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

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Downstream Successor

CFMZSMGAMPBRBE-UHFFFAOYSA-N

N-Hydroxyphthalimide

C1=CC=C2C(=C1)C(=O)N(C2=O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Environmental

Downstream Successor

CFMZSMGAMPBRBE-UHFFFAOYSA-N

N-Hydroxyphthalimide

C1=CC=C2C(=C1)C(=O)N(C2=O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Downstream Successor

QIWKCQDJZPRXNS-UHFFFAOYSA-N

N-(o-Carboxybenzoyl)-DL-glutamic acid

OC(=O)CCC(C(=O)O)NC(=O)C1=CC=CC=C1C(=O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Downstream Successor

RDVIGUDHFHRUKP-UHFFFAOYSA-N

2-(4-Hydroxyphthalimido)glutaric acid

OC(=O)CCC(C(=O)O)N1C(=O)C2=CC=C(C=C2C1=O)O

Precursor

FEFFSKLJNYRHQN-UHFFFAOYSA-N

N-Phthaloyl-DL-glutamic acid

c1ccc2c(c1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O

Abiotic

Downstream Successor

FWTQBDLDGNNHLC-UHFFFAOYSA-N

OC(=O)CCC(C(=O)O)N1C(=O)C2C=CC(=O)C=C2C1=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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.