Search More · GCI-TPs

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

7 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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

Upstream Precursor

TUZAVLAUJHUFLA-UHFFFAOYSA-N

Bz-Arg-4-Abz-OH.HCl

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)C(=O)O

Abiotic

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

TUZAVLAUJHUFLA-UHFFFAOYSA-N

Bz-Arg-4-Abz-OH.HCl

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)C(=O)O

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

TUZAVLAUJHUFLA-UHFFFAOYSA-N

Bz-Arg-4-Abz-OH.HCl

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)C(=O)O

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

RKDYKIHMFYAPMZ-UHFFFAOYSA-N

Benzoyl-DL-arginine p-nitroanilide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

RKDYKIHMFYAPMZ-UHFFFAOYSA-N

Benzoyl-DL-arginine p-nitroanilide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

RKDYKIHMFYAPMZ-UHFFFAOYSA-N

Benzoyl-DL-arginine p-nitroanilide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

RKDYKIHMFYAPMZ-UHFFFAOYSA-N

Benzoyl-DL-arginine p-nitroanilide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

RKDYKIHMFYAPMZ-UHFFFAOYSA-N

Benzoyl-DL-arginine p-nitroanilide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

DEFAKPKFXYITPZ-UHFFFAOYSA-N

N-(4-((Aminoiminomethyl)amino)-1-((2-naphthalenylamino)carbonyl)butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC3=CC=CC=C3C=C2

Environmental

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Upstream Precursor

YXDSWEZHWDTWLL-FQEVSTJZSA-N

N-[(2S)-5-(diaminomethylideneamino)-1-[(4-methoxynaphthalen-2-yl)amino]-1-oxopentan-2-yl]benzamide

COC1=CC(=CC2=CC=CC=C21)NC(=O)[C@H](CCCN=C(N)N)NC(=O)C3=CC=CC=C3

Abiotic

Product

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Abiotic

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

KXDAEFPNCMNJSK-UHFFFAOYSA-N

Benzamide

C1=CC=CC(=C1)C(=O)N

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Abiotic

Downstream Successor

ULEBESPCVWBNIF-UHFFFAOYSA-N

2-Amino-5-(diaminomethylideneamino)pentanamide

NC(CCCN=C(N)N)C(=O)N

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

ULEBESPCVWBNIF-UHFFFAOYSA-N

2-Amino-5-(diaminomethylideneamino)pentanamide

NC(CCCN=C(N)N)C(=O)N

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Abiotic

Downstream Successor

BMFMQGXDDJALKQ-UHFFFAOYSA-N

5-Guanidino-2-hydroxypentanoic acid

C(CC(C(=O)O)O)CN=C(N)N

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

BMFMQGXDDJALKQ-UHFFFAOYSA-N

5-Guanidino-2-hydroxypentanoic acid

C(CC(C(=O)O)O)CN=C(N)N

Precursor

UMKJQJGLFKDADN-UHFFFAOYSA-N

N-(1-(aminocarbonyl)-4-{[amino(imino)methyl]amino}butyl)benzamide

C1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)N

Environmental

Downstream Successor

SWVVCZUQYOEUQV-UHFFFAOYSA-N

5-(Diaminomethylideneamino)-2-hydroxypentanamide

C(CC(C(=O)N)O)CN=C(N)N

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

No Original Precursors

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