Search More · GCI-TPs

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

Precursor

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

11 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

6 steps

Dead-End Product

LXNSRSYDQMJXSI-KTAJNNJTSA-N

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

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

5 steps

Dead-End Product

OZMYWEVXZYFPQA-KTAJNNJTSA-N

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

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

5 steps

Dead-End Product

PVWXFQHGTABOBD-HYXAFXHYSA-N

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

Previewing top 9 entries. If you want the full results, please use the download button above.

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

DHMQDGOQFOQNFH-UHFFFAOYSA-N

Glycine

C(CN)(O)=O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

LYIIBVSRGJSHAV-UHFFFAOYSA-N

Aminoacetaldehyde

NCC=O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

PIICEJLVQHRZGT-UHFFFAOYSA-N

Ethylenediamine

NCCN

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

RPNUMPOLZDHAAY-UHFFFAOYSA-N

Diethylenetriamine

C(CN)NCCN

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

FEGRFLSNPCOSRJ-UHFFFAOYSA-N

2-((2-Aminoethyl)amino)acetaldehyde

C(CN)NCC=O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

BKSKQIPHTTWTDW-UHFFFAOYSA-N

2-[(2-Hydroxyethyl)amino]acetaldehyde

N(CC=O)CCO

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

VILCJCGEZXAXTO-UHFFFAOYSA-N

Triethylenetetramine

N(CCN)CCNCCN

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

PEJTZZJLRKCVBP-UHFFFAOYSA-N

2-[2-(2-Aminoethylamino)ethylamino]acetaldehyde

C(CNCCNCCN)=O

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Abiotic

Downstream Successor

FAGUFWYHJQFNRV-UHFFFAOYSA-N

Tetraethylenepentamine

C(CNCCNCCNCCN)N

Precursor

LRSGPYSVXWNMKD-UHFFFAOYSA-N

21-amino-N-(2-((2-((2-((2-aminoethyl)amino)ethyl)amino)ethyl)amino)ethyl)-9-(1-hydroxynonyl)-9,12,15,18-tetraazahenicosanamide

CCCCCCCCC(C(CCCCCCCC(=O)NCCNCCNCCNCCN)NCCNCCNCCNCCN)O

Environmental

Downstream Successor

FAGUFWYHJQFNRV-UHFFFAOYSA-N

Tetraethylenepentamine

C(CNCCNCCNCCN)N

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

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

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