Search More · GCI-TPs

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

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

12 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

17 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

17 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

19 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

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

Upstream Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Abiotic

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Upstream Precursor

GERJHTAILGEDCS-UHFFFAOYSA-N

CCCC(=O)NC(CC1=CC(=C(C=C1)O)Cl)C(=O)NCCCNCCCCNCCCN

Environmental

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Upstream Precursor

GERJHTAILGEDCS-UHFFFAOYSA-N

CCCC(=O)NC(CC1=CC(=C(C=C1)O)Cl)C(=O)NCCCNCCCCNCCCN

Abiotic

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Upstream Precursor

GERJHTAILGEDCS-UHFFFAOYSA-N

CCCC(=O)NC(CC1=CC(=C(C=C1)O)Cl)C(=O)NCCCNCCCCNCCCN

Abiotic

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Upstream Precursor

GERJHTAILGEDCS-UHFFFAOYSA-N

CCCC(=O)NC(CC1=CC(=C(C=C1)O)Cl)C(=O)NCCCNCCCCNCCCN

Environmental

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Upstream Precursor

NZWKBAAJWUHDSR-UHFFFAOYSA-N

CCCC(=O)NC(CC1=CC(=C(C(=C1)Cl)O)Cl)C(=O)NCCCNCCCCNCCCN

Abiotic

Product

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Previewing top 6 entries. If you want the full results, please use the download button above.

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Abiotic

Downstream Successor

FERIUCNNQQJTOY-UHFFFAOYSA-N

Butyric Acid

C(CCC)(O)=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

FERIUCNNQQJTOY-UHFFFAOYSA-N

Butyric Acid

C(CCC)(O)=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

AKXKFZDCRYJKTF-UHFFFAOYSA-N

Reuterin

C(CC=O)O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

PCXDJQZLDDHMGX-UHFFFAOYSA-N

Propanal, 3-amino-

NCCC=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

XFNJVJPLKCPIBV-UHFFFAOYSA-N

1,3-Propanediamine

C(CN)CN

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

DNSISZSEWVHGLH-UHFFFAOYSA-N

Butyramide

NC(CCC)=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Abiotic

Downstream Successor

DNSISZSEWVHGLH-UHFFFAOYSA-N

Butyramide

NC(CCC)=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Environmental

Downstream Successor

DNSISZSEWVHGLH-UHFFFAOYSA-N

Butyramide

NC(CCC)=O

Precursor

DTWANULJDRVTFI-UHFFFAOYSA-N

N-[3-[[4-[(3-Aminopropyl)amino]butyl]amino]propyl]-4-hydroxy-alpha-[(1-oxobutyl)amino]benzenepropanamide

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)NCCCNCCCCNCCCN

Abiotic

Downstream Successor

VURXKSHTHQFAQS-UHFFFAOYSA-N

2-(Butanoylamino)-3-(4-hydroxyphenyl)propanoic acid

CCCC(=O)NC(CC1=CC=C(C=C1)O)C(=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.

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