Search More · GCI-TPs

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Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

4 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

RHEQJJIPJSSFDP-UHFFFAOYSA-O

CC[S+](CCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)=O)Cl

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

LIDCXUIQZSKVQO-UHFFFAOYSA-N

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)=O

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

LIDCXUIQZSKVQO-UHFFFAOYSA-N

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)=O

Environmental

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

LIDCXUIQZSKVQO-UHFFFAOYSA-N

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)=O

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

ZYZPYRVCJRRZQC-UHFFFAOYSA-O

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCC[S+](CC)Cl

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

JRUDIXBODSNWIA-UHFFFAOYSA-N

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)(=O)=O

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Upstream Precursor

QQJRITRHFCHEBO-UHFFFAOYSA-N

CCS(CCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCS(CC)=O)=O

Abiotic

Product

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

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

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

DGVVWUTYPXICAM-UHFFFAOYSA-N

2-Mercaptoethanol

OCCS

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

DNJIEGIFACGWOD-UHFFFAOYSA-N

Ethanethiol

CCS

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Abiotic

Downstream Successor

DNJIEGIFACGWOD-UHFFFAOYSA-N

Ethanethiol

CCS

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

DNJIEGIFACGWOD-UHFFFAOYSA-N

Ethanethiol

CCS

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

GUCBUVXBLCUMPZ-UHFFFAOYSA-N

3-(Aminomethyl)benzaldehyde

C1=CC(=CC(=C1)CN)C=O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Abiotic

Downstream Successor

GUCBUVXBLCUMPZ-UHFFFAOYSA-N

3-(Aminomethyl)benzaldehyde

C1=CC(=CC(=C1)CN)C=O

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Abiotic

Downstream Successor

FDLQZKYLHJJBHD-UHFFFAOYSA-N

1,3-Benzenedimethanamine

NCc1cccc(c1)CN

Precursor

YWYGCKLOQIMVCI-UHFFFAOYSA-N

1-(2-Ethylsulfanylethyl)-3-[[3-[(2-ethylsulfanylethylcarbamoylamino)methyl]phenyl]methyl]urea

CCSCCNC(=O)NCC1=CC(=CC=C1)CNC(=O)NCCSCC

Environmental

Downstream Successor

FDLQZKYLHJJBHD-UHFFFAOYSA-N

1,3-Benzenedimethanamine

NCc1cccc(c1)CN

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

No Original Precursors

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