Search More · GCI-TPs

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

Upstream Precursor

HYAFETHFCAUJAY-UHFFFAOYSA-N

Pioglitazone

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)S3

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

HYAFETHFCAUJAY-UHFFFAOYSA-N

Pioglitazone

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)S3

Environmental

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

HYAFETHFCAUJAY-UHFFFAOYSA-N

Pioglitazone

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)S3

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

GAMHVUDORKUXFO-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-1-oxo-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)S3=O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

XBSDTROMDVOABL-UHFFFAOYSA-N

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)S3(=O)=O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

GNIYIMIGTRZUPL-UHFFFAOYSA-N

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3=O)O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

WLDVNJMEAWRPJF-UHFFFAOYSA-N

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)[S+]3Cl)O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

SMZVWNWMJCDBPK-UHFFFAOYSA-O

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)NC(=O)[S+]3Cl

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Upstream Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Product

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

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

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

KKADPXVIOXHVKN-UHFFFAOYSA-N

4-Hydroxyphenylpyruvic Acid

OC(=O)C(CC1=CC=C(C=C1)O)=O

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

YNRKXBSUORGBIU-UHFFFAOYSA-N

Thiohydroxamsaure

C(=S)(NO)O

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

CKPRPBAANRHUNY-UHFFFAOYSA-N

OC1=CC=C(C=C1)CC2C(=O)N(C(=O)S2)O

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

CKPRPBAANRHUNY-UHFFFAOYSA-N

OC1=CC=C(C=C1)CC2C(=O)N(C(=O)S2)O

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

CKPRPBAANRHUNY-UHFFFAOYSA-N

OC1=CC=C(C=C1)CC2C(=O)N(C(=O)S2)O

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

OUJMXIPHUCDRAS-UHFFFAOYSA-N

5-Ethyl-2-pyridineethanol

CCC1=CN=C(C=C1)CCO

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

OUJMXIPHUCDRAS-UHFFFAOYSA-N

5-Ethyl-2-pyridineethanol

CCC1=CN=C(C=C1)CCO

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

OUJMXIPHUCDRAS-UHFFFAOYSA-N

5-Ethyl-2-pyridineethanol

CCC1=CN=C(C=C1)CCO

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

NQQYNWRMNDJLKG-UHFFFAOYSA-N

oxocarbamothioic S-acid

C(=O)(N=O)S

Precursor

XLJQTZALGFITPY-UHFFFAOYSA-N

5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-3-hydroxy-1,3-thiazolidine-2,4-dione

CCC1=CN=C(C=C1)CCOC2=CC=C(C=C2)CC3C(=O)N(C(=O)S3)O

Abiotic

Downstream Successor

KFUWSJNHJGDTBY-UHFFFAOYSA-N

2-(5-Ethylpyridin-2-YL)acetaldehyde

CCC1=CN=C(C=C1)CC=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.

No Dead-Ends

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

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