Search More · GCI-TPs

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

13 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

10 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

13 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

13 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

3 steps

Dead-End Product

LYGJENNIWJXYER-UHFFFAOYSA-N

Nitromethane

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

3 steps

Dead-End Product

ADCROEZEFWMOOY-UHFFFAOYSA-N

Methanamine, N-methylene-, N-oxide

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

6 steps

Dead-End Product

UEAPBSCGXILXLY-UHFFFAOYSA-N

OC(=O)CS(=O)=O

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

7 steps

Dead-End Product

FNKQFBWKNIGIOS-UHFFFAOYSA-N

Furan-2,5-diol

c1c(oc(c1)O)O

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

Upstream Precursor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Environmental

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Environmental

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

CCTNCMQFNYAVGH-UHFFFAOYSA-N

1-N'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfonyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)(=O)=O

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Upstream Precursor

CCTNCMQFNYAVGH-UHFFFAOYSA-N

1-N'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfonyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)(=O)=O

Abiotic

Product

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Downstream Successor

ROSDSFDQCJNGOL-UHFFFAOYSA-O

Dimethylaminium

C[NH2+]C

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

ROSDSFDQCJNGOL-UHFFFAOYSA-O

Dimethylaminium

C[NH2+]C

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

NESLOYMMIUOLMU-UHFFFAOYSA-N

(1-Amino-2-nitroethenyl)(methyl)amine

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

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

PXXMACVFIPNJOH-UHFFFAOYSA-N

NC(=C[N+](=O)[O-])NCCS(=O)CC1=CC=C(O1)CN(C)C

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Downstream Successor

VMXUWOKSQNHOCA-UHFFFAOYSA-O

Dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium

CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)C[NH+](C)C

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

CMHAMFZTWQLSGA-UHFFFAOYSA-N

2-[[5-[(Dimethylamino)methyl]furan-2-yl]methylsulfinyl]acetaldehyde

C(CS(=O)CC1=CC=C(O1)CN(C)C)=O

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Abiotic

Downstream Successor

CMHAMFZTWQLSGA-UHFFFAOYSA-N

2-[[5-[(Dimethylamino)methyl]furan-2-yl]methylsulfinyl]acetaldehyde

C(CS(=O)CC1=CC=C(O1)CN(C)C)=O

Precursor

SKHXRNHSZTXSLP-UHFFFAOYSA-N

Ranitidine S-oxide

CNC(=C[N+](=O)[O-])NCCS(CC1=CC=C(O1)CN(C)C)=O

Environmental

Downstream Successor

CMHAMFZTWQLSGA-UHFFFAOYSA-N

2-[[5-[(Dimethylamino)methyl]furan-2-yl]methylsulfinyl]acetaldehyde

C(CS(=O)CC1=CC=C(O1)CN(C)C)=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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