Exact Mass: 852.2054105999999

4-Aminobutanoyl-CoA

C25H43N8O17P3S (852.168)

An aminobutanoyl-CoA resulting from the formal condensation of the thiol group of coenzyme A with the carboxylic acid group of 4-aminobutanoic acid.

L-3-Aminobutyryl-CoA

C25H43N8O17P3S (852.168)

L-3-Aminobutyryl-CoA is found in the lysine fermentation to acetate and butyrate pathway. L-3-Aminobutyryl-CoA is produced from a reaction between (S)-5-amino-3-oxohexanoate and acetyl-CoA, with acetoacetate as a byproduct. L-3-aminobutyryl-CoA breaks down to form ammonia and crotonyl-CoA, a reaction catalyzed by 3-aminobutyryl-CoA ammonia-lyase. L-3-Aminobutyryl-CoA is found in the lysine fermentation to acetate and butyrate pathway. L-3-Aminobutyryl-CoA is produced from a reaction between (S)-5-amino-3-oxohexanoate and acetyl-CoA, with acetoacetate as a byproduct.

3-aminobutyryl-CoA

C25H43N8O17P3S (852.168)

An aminobutanoyl-CoA resulting from the formal condensation of the thiol group of coenzyme A with the carboxy group of 3-aminobutanoic acid.

Smilaside H

C42H44O19 (852.2477)

Smilaside I

C42H44O19 (852.2477)

1beta,3beta,4beta-trihydroxy-5alpha-{[3-[4-[1beta-(6-O-(5-(E)-caffeoylquinic acid)-beta-D-glucopyranosyl)oxy]-3-hydroxyphenyl]-(E)-1-oxo-2-propenyl]oxy}cyclohexanecarboxylic acid|viarumacid A

C38H44O22 (852.2324)

joziknipholone A|joziknipholone B

C48H36O15 (852.2054)

(1,3-O-di-p-coumaroyl-6-O-feruloyl)-beta-D-fructofuranosyl-(2->1)-(6-O-acetyl)-alpha-D-glucopyranoside|smilaside I

C42H44O19 (852.2477)

6-O-[4-O-(6-O-syringyloyl-beta-D-glucopyranosyl)vanilloyl]-beta-D-glucopyranosyl 4-hydroxy-3,5-dimethylbenzoate

C38H44O22 (852.2324)

(1,3-O-di-p-coumaroyl-6-O-feruloyl)-beta-D-fructofuranosyl-(2->1)-(2-O-acetyl)-alpha-D-glucopyranoside|smilaside H

C42H44O19 (852.2477)

3S-aminobutanoyl-CoA

C25H43N8O17P3S (852.168)

Bis(4-dodecylphenyl)iodoniumhexaflurorantimonate

C36H58F6ISb (852.2525)

1,2,3-Propanetriyl tri(2H29)pentadecanoate

C48H5D87O6 (852.2355)

(S)-(-)-[(S)-2-DI(3,5-XYLYL)PHOSPHINOFERROCENYL][2-DI(4-TRIFLUOROMETHYLPHENYL)PHOSPHINOPHENYL]METHANOL

C47H40F6FeOP2 (852.1808)

2,5-Dihydro-2,5-dioctyl-3,6-bis[5-(trimethylstannyl)-2-thienyl]pyrrolo[3,4-c]pyrrole-1,4-dione

C36H56N2O2S2Sn2 (852.1827)

(OC-6-33)-Bis[3,5-difluoro-2-(2-pyridinyl-kN)phenyl-kC][tetrakis(1H-pyrazolato-kN1)borato(1-)-kN2,kN2]-iridium

C34H24BF4IrN10 (852.1844)

Disodium 2-(3-{4-tert-butyl-7-[ethyl(3-sulfonatopropyl)amino]chromenium-2-yl}prop-2-en-1-ylidene)-3-(3-carboxypropyl)-3-methyl-1-(3-sulfonatopropyl)indoline-5-sulfonate

C37H46N2Na2O12S3 (852.2008)

Disodium 2-(3-{2-tert-butyl-7-[ethyl(3-sulfonatopropyl)amino]chromenium-4-yl}prop-2-en-1-ylidene)-3-(3-carboxypropyl)-3-methyl-1-(3-sulfonatopropyl)indoline-5-sulfonate

C37H46N2Na2O12S3 (852.2008)

Dimethylglycine-CoA; (Acyl-CoA); [M+H]+

C25H43N8O17P3S (852.168)

Alpha-Aminobutyric Acid-CoA; (Acyl-CoA); [M+H]+

C25H43N8O17P3S (852.168)

Alpha-Aminoisobutyric Acid-CoA; (Acyl-CoA); [M+H]+

C25H43N8O17P3S (852.168)

L-3-aminobutanoyl-CoA

C25H43N8O17P3S (852.168)

A 3-aminobutyryl-CoA having that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of L-3-aminobutanoic acid.

Aminobutanoyl-CoA

C25H43N8O17P3S (852.168)

(5-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-4-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl)methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

[(2r,3r,4s,5s)-5-{[(2r,3r,4s,5s,6r)-6-[(acetyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxy-4-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

(9's)-1',5-bis(3-acetyl-2,6-dihydroxy-4-methoxyphenyl)-1,4',5',8-tetrahydroxy-2',6-dimethyl-9'h-[2,9'-bianthracene]-9,10,10'-trione

C48H36O15 (852.2054)

[(2r,3s,4s,5s)-5-{[(2r,3r,4s,5s,6r)-6-[(acetyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy}-4-hydroxy-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

1',5-bis(3-acetyl-2,6-dihydroxy-4-methoxyphenyl)-1,4',5',8-tetrahydroxy-2',6-dimethyl-9'h-[2,9'-bianthracene]-9,10,10'-trione

C48H36O15 (852.2054)

[5-({6-[(acetyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl}oxy)-3-hydroxy-4-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

[(2r,3r,4s,5s)-5-{[(2r,3r,4s,5s,6r)-3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-4-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

(1s,3r,4r,5r)-3-{[(2e)-3-(4-{[(2s,3r,4s,5s,6r)-6-{[(1s,3r,4r,5r)-3-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexanecarbonyloxy]methyl}-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid

C38H44O22 (852.2324)

3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

C38H44O22 (852.2324)

[(2r,3s,4s,5s)-5-{[(2r,3r,4s,5s,6r)-3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-hydroxy-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5-({[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxolan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C42H44O19 (852.2477)

(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3-methoxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoyloxy)methyl]oxan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

C38H44O22 (852.2324)