Search More · GCI-TPs

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

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

6 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

7 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

4 steps

Dead-End Product

CCGKOQOJPYTBIH-UHFFFAOYSA-N

Ketene

C(=C)=O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

7 steps

Dead-End Product

PEKFLTXLZKCYTB-UHFFFAOYSA-N

C(=O)(CN(C(=O)O)Cl)O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

3 steps

Dead-End Product

WXJOJAFDOAYUNG-UHFFFAOYSA-N

C(=O)(N(CCCCCCN(C(=O)O)Cl)Cl)O

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

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

WERYXYBDKMZEQL-UHFFFAOYSA-N

1,4-Butanediol

C(CCO)CO

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

Abiotic

Downstream Successor

XXMIOPMDWAUFGU-UHFFFAOYSA-N

1,6-Hexanediol

C(CCCO)CCO

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

XXMIOPMDWAUFGU-UHFFFAOYSA-N

1,6-Hexanediol

C(CCCO)CCO

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

FPFTWHJPEMPAGE-UHFFFAOYSA-N

Hexanal, 6-hydroxy-

C(CCCO)CC=O

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

HDIHOAXFFROQHR-UHFFFAOYSA-N

Hexamethylenediamine carbamate

C(CCCNC(=O)O)CCN

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

Abiotic

Downstream Successor

HMBNQNDUEFFFNZ-UHFFFAOYSA-N

1,4-Butanediol monovinyl ether

C=COCCCCO

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

HMBNQNDUEFFFNZ-UHFFFAOYSA-N

1,4-Butanediol monovinyl ether

C=COCCCCO

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

Abiotic

Downstream Successor

APKFLZGRWMXNNV-UHFFFAOYSA-L

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

Precursor

HYUMTLCJAKNRKM-UHFFFAOYSA-N

11,18-Dioxa-2,9,20,27-tetraazaoctacosanedioic acid, 10,19-dioxo-, 1,28-bis(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)NCCCCCCNC(=O)OCCCCCCOC(=O)NCCCCCCNC(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

APKFLZGRWMXNNV-UHFFFAOYSA-L

N(C(=O)[O-])CCCCCCNC(=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.

No All Precursors

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