Exact Mass: 563.1943924
Exact Mass Matches: 563.1943924
Found 263 metabolites which its exact mass value is equals to given mass value 563.1943924
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
UR-12947
C26H37N5O5S2 (563.2235992000001)
Elacridar
C1744 - Multidrug Resistance Modulator
Thiocolchicoside
Thiocolchicoside
N-[(7S)-1,2-dimethoxy-10-(methylthio)-9-oxo-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide is a glycoside. Thiocolchicoside is a semi-synthetic derivative of the colchicine, a natural anti-inflammatory glycoside which originates from the flower seeds of Superba gloriosa. It is a muscle relaxant with anti-inflammatory and analgesic effects. It has potent convulsant activity and should not be administered to individuals prone to seizures. M - Musculo-skeletal system > M03 - Muscle relaxants > M03B - Muscle relaxants, centrally acting agents C78281 - Agent Affecting Musculoskeletal System > C29696 - Muscle Relaxant Thiocolchicoside is a competitive γ-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist in the central nervous system. Thiocolchicoside is a semisynthetic sulfur derivative of colchicoside. Thiocolchicoside is a muscle relaxant and has anti-inflammatory, and analgesic properties[1]. Thiocolchicoside is a competitive γ-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist in the central nervous system. Thiocolchicoside is a semisynthetic sulfur derivative of colchicoside. Thiocolchicoside is a muscle relaxant and has anti-inflammatory, and analgesic properties[1].
Ondena
Daunorubicin hydrochloride appears as orange-red powder. Thin red needles decomposing at 188-190 °C. An anti-cancer drug. Daunorubicin hydrochloride is an anthracycline. Daunorubicin Hydrochloride is the hydrochloride salt of an anthracycline antineoplastic antibiotic with therapeutic effects similar to those of doxorubicin. Daunorubicin exhibits cytotoxic activity through topoisomerase-mediated interaction with DNA, thereby inhibiting DNA replication and repair and RNA and protein synthesis. A very toxic anthracycline aminoglycoside antineoplastic isolated from Streptomyces peucetius and others, used in treatment of LEUKEMIA and other NEOPLASMS. C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor D000970 - Antineoplastic Agents > D059003 - Topoisomerase Inhibitors > D059005 - Topoisomerase II Inhibitors C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C259 - Antineoplastic Antibiotic C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor > C1748 - Topoisomerase Inhibitor C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D004791 - Enzyme Inhibitors Daunorubicin (Daunomycin) hydrochloride is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin hydrochloride inhibits DNA and RNA synthesis. Daunorubicin hydrochloride is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin hydrochloride is also an anthracycline antibiotic. Daunorubicin hydrochloride can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor[1][2][4][5].
7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzo[1,4]thiazine-3,5-dione-(2-O-caffeoyl)-beta-D-glucopyranoside
C26H29NO11S (563.1461244000001)
Ravidomycin
A C-glycosylated naphthoisochromene derivative obtained from Streptomyces ravidus; exhibits antibiotic and anticancer properties.
Daunorubicin HCl (Daunomycin HCl)
C27H30ClNO10 (563.1558150000001)
Cys Gln Gln Trp
Cys Gln Trp Gln
Cys Trp Gln Gln
Asp Asp Glu Trp
Asp Asp Trp Glu
Asp Glu Asp Trp
Asp Glu Trp Asp
Asp Phe Pro Trp
Asp Phe Trp Pro
Asp Ile Met Trp
Asp Ile Trp Met
Asp Leu Met Trp
Asp Leu Trp Met
Asp Met Ile Trp
Asp Met Leu Trp
Asp Met Trp Ile
Asp Met Trp Leu
Asp Pro Phe Trp
Asp Pro Trp Phe
Asp Trp Asp Glu
Asp Trp Glu Asp
Asp Trp Phe Pro
Asp Trp Ile Met
Asp Trp Leu Met
Asp Trp Met Ile
Asp Trp Met Leu
Asp Trp Pro Phe
Glu Asp Asp Trp
Glu Asp Trp Asp
Glu Glu Met Arg
C21H37N7O9S (563.2373352000001)
Glu Glu Arg Met
C21H37N7O9S (563.2373352000001)
Glu Glu Thr Trp
Glu Glu Trp Thr
Glu Met Glu Arg
C21H37N7O9S (563.2373352000001)
Glu Met Arg Glu
C21H37N7O9S (563.2373352000001)
Glu Met Val Trp
Glu Met Trp Val
Glu Arg Glu Met
C21H37N7O9S (563.2373352000001)
Glu Arg Met Glu
C21H37N7O9S (563.2373352000001)
Glu Thr Glu Trp
Glu Thr Trp Glu
Glu Val Met Trp
Glu Val Trp Met
Glu Trp Asp Asp
Glu Trp Glu Thr
Glu Trp Met Val
Glu Trp Thr Glu
Glu Trp Val Met
Phe Asp Pro Trp
Phe Asp Trp Pro
Phe Pro Asp Trp
Phe Pro Trp Asp
Phe Trp Asp Pro
Phe Trp Pro Asp
His Met Asn Tyr
His Met Tyr Asn
His Asn Met Tyr
His Asn Tyr Met
His Tyr Met Asn
His Tyr Asn Met
Ile Asp Met Trp
Ile Asp Trp Met
Ile Met Asp Trp
Ile Met Trp Asp
Ile Trp Asp Met
Ile Trp Met Asp
Leu Asp Met Trp
Leu Asp Trp Met
Leu Met Asp Trp
Leu Met Trp Asp
Leu Trp Asp Met
Leu Trp Met Asp
Met Asp Ile Trp
Met Asp Leu Trp
Met Asp Trp Ile
Met Asp Trp Leu
Met Glu Glu Arg
C21H37N7O9S (563.2373352000001)
Met Glu Arg Glu
C21H37N7O9S (563.2373352000001)
Met Glu Val Trp
Met Glu Trp Val
Met His Asn Tyr
Met His Tyr Asn
Met Ile Asp Trp
Met Ile Trp Asp
Met Leu Asp Trp
Met Leu Trp Asp
Met Met Pro Trp
C26H37N5O5S2 (563.2235992000001)
Met Met Trp Pro
C26H37N5O5S2 (563.2235992000001)
Met Asn His Tyr
Met Asn Asn Trp
Met Asn Trp Asn
Met Asn Tyr His
Met Pro Met Trp
C26H37N5O5S2 (563.2235992000001)
Met Pro Trp Met
C26H37N5O5S2 (563.2235992000001)
Met Arg Glu Glu
C21H37N7O9S (563.2373352000001)
Met Val Glu Trp
Met Val Trp Glu
Met Trp Asp Ile
Met Trp Asp Leu
Met Trp Glu Val
Met Trp Ile Asp
Met Trp Leu Asp
Met Trp Met Pro
C26H37N5O5S2 (563.2235992000001)
Met Trp Asn Asn
Met Trp Pro Met
C26H37N5O5S2 (563.2235992000001)
Met Trp Val Glu
Met Tyr His Asn
Met Tyr Asn His
Asn His Met Tyr
Asn His Tyr Met
Asn Met His Tyr
Asn Met Asn Trp
Asn Met Trp Asn
Asn Met Tyr His
Asn Asn Met Trp
Asn Asn Trp Met
Asn Trp Met Asn
Asn Trp Asn Met
Asn Tyr His Met
Asn Tyr Met His
Pro Asp Phe Trp
Pro Asp Trp Phe
Pro Phe Asp Trp
Pro Phe Trp Asp
Pro Met Met Trp
C26H37N5O5S2 (563.2235992000001)
Pro Met Trp Met
C26H37N5O5S2 (563.2235992000001)
Pro Trp Asp Phe
Pro Trp Phe Asp
Pro Trp Met Met
C26H37N5O5S2 (563.2235992000001)
Gln Cys Gln Trp
Gln Cys Trp Gln
Gln Gln Cys Trp
Gln Gln Trp Cys
Gln Trp Cys Gln
Gln Trp Gln Cys
Arg Glu Glu Met
C21H37N7O9S (563.2373352000001)
Arg Glu Met Glu
C21H37N7O9S (563.2373352000001)
Arg Met Glu Glu
C21H37N7O9S (563.2373352000001)
Thr Glu Glu Trp
Thr Glu Trp Glu
Thr Trp Glu Glu
Val Glu Met Trp
Val Glu Trp Met
Val Met Glu Trp
Val Met Trp Glu
Val Trp Glu Met
Val Trp Met Glu
Trp Cys Gln Gln
Trp Asp Asp Glu
Trp Asp Glu Asp
Trp Asp Phe Pro
Trp Asp Ile Met
Trp Asp Leu Met
Trp Asp Met Ile
Trp Asp Met Leu
Trp Asp Pro Phe
Trp Glu Asp Asp
Trp Glu Glu Thr
Trp Glu Met Val
Trp Glu Thr Glu
Trp Glu Val Met
Trp Phe Asp Pro
Trp Phe Pro Asp
Trp Ile Asp Met
Trp Ile Met Asp
Trp Leu Asp Met
Trp Leu Met Asp
Trp Met Asp Ile
Trp Met Asp Leu
Trp Met Glu Val
Trp Met Ile Asp
Trp Met Leu Asp
Trp Met Met Pro
C26H37N5O5S2 (563.2235992000001)
Trp Met Asn Asn
Trp Met Pro Met
C26H37N5O5S2 (563.2235992000001)
Trp Met Val Glu
Trp Asn Met Asn
Trp Asn Asn Met
Trp Pro Asp Phe
Trp Pro Phe Asp
Trp Pro Met Met
C26H37N5O5S2 (563.2235992000001)
Trp Gln Cys Gln
Trp Gln Gln Cys
Trp Thr Glu Glu
Trp Val Glu Met
Trp Val Met Glu
Tyr His Met Asn
Tyr His Asn Met
Tyr Met His Asn
Tyr Met Asn His
Tyr Asn His Met
Tyr Asn Met His
(7S,9S)-9-acetyl-7-[(2R,4S,5R,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,9,11-trihydroxy-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione,hydrochloride
C27H30ClNO10 (563.1558150000001)
3-[[4-[[diamino(phenylazo)phenyl]azo]-1-naphthyl]azo]-N,N,N-trimethylanilinium chloride
Trimetrexate glucuronate
C471 - Enzyme Inhibitor > C2153 - Dihydrofolate Reductase Inhibitor
Esorubicin hydrochloride
C27H30ClNO10 (563.1558150000001)
C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C259 - Antineoplastic Antibiotic C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor > C1748 - Topoisomerase Inhibitor C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D000970 - Antineoplastic Agents
Daunorubicin Hydrochloride
C27H30ClNO10 (563.1558150000001)
C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor D000970 - Antineoplastic Agents > D059003 - Topoisomerase Inhibitors > D059005 - Topoisomerase II Inhibitors C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C259 - Antineoplastic Antibiotic C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor > C1748 - Topoisomerase Inhibitor C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D004791 - Enzyme Inhibitors Daunorubicin (Daunomycin) hydrochloride is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin hydrochloride inhibits DNA and RNA synthesis. Daunorubicin hydrochloride is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin hydrochloride is also an anthracycline antibiotic. Daunorubicin hydrochloride can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor[1][2][4][5].
4,7,9-trihydroxy-1,3-dimethyl-5-(4,7,9-trihydroxy-1,3-dimethyl-5,10-dioxo-3,4-dihydro-1H-benzo[g]isochromen-6-yl)-3,4-dihydro-1H-benzo[g]isochromen-10-olate
[(2S,3R,4S,5S,6R)-4-amino-2-[(1S,2S,3R,4S,6R)-4,6-diamino-3-[(2R,3R,4R,5S,6R)-3-amino-6-(aminomethyl)-4,5-dihydroxyoxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-3-yl] dihydrogen phosphate
2-amino-N-[[(1R,2S,10R,12R,13S)-12-cyano-7,18-dimethoxy-6,17,21-trimethyl-5,8,16,19-tetraoxo-11,21-diazapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-4(9),6,15(20),17-tetraen-10-yl]methyl]propanamide
Gadolinium(2+);1-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetrazacyclododec-1-yl]propan-2-yloxidanium
V - Various > V08 - Contrast media > V08C - Magnetic resonance imaging contrast media > V08CA - Paramagnetic contrast media
(2S)-2-(benzenesulfonamido)-3-[[2-(4-piperidin-4-ylpiperidin-1-yl)-4-propan-2-yl-1,3-thiazole-5-carbonyl]amino]propanoic acid
C26H37N5O5S2 (563.2235992000001)
Asn-Met-Trp-Asn
A tetrapeptide composed of L-asparagine, L-methionine, L-tryptophan and L-asparagine joined in sequence by peptide linkages.
Protoaphin aglucone(1-)
A phenolate anion that is the conjugate base of protoaphin aglucone, obtained by deprotonation of the phenolic hydroxy group at position 7; major species at pH 7.3.
N-[9-{3-[(2,5-dioxopyrrolidin-1-yl)oxy]-3-oxopropyl}-6-(ethylamino)-2,7-dimethyl-3H-xanthen-3-ylidene]ethanaminium perchlorate
2-[(2R,4aR,12aR)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
2-fluoro-N-[[(4R,5S)-2-[(2R)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4S,5R)-2-[(2S)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4R,5R)-2-[(2R)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-[(2R,4aR,12aS)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
2-fluoro-N-[[(4S,5S)-2-[(2R)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4R,5S)-2-[(2S)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4S,5R)-2-[(2R)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4S,5S)-2-[(2S)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
2-fluoro-N-[[(4R,5R)-2-[(2S)-1-hydroxypropan-2-yl]-4-methyl-1,1-dioxo-8-pyridin-4-yl-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methylbenzenesulfonamide
(3R)-2-[(R)-tert-butylsulfinyl]-4-[3-(3-fluorophenyl)phenyl]-3-(2-hydroxyethyl)-N-(2,2,2-trifluoroethyl)-1,3-dihydropyrrolo[3,4-c]pyridine-6-carboxamide
(3S)-2-[(S)-tert-butylsulfinyl]-4-[3-(3-fluorophenyl)phenyl]-3-(2-hydroxyethyl)-N-(2,2,2-trifluoroethyl)-1,3-dihydropyrrolo[3,4-c]pyridine-6-carboxamide
N-[[(4R,5R)-2-[(2R)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4S,5S)-2-[(2S)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4R,5R)-2-[(2S)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
2,2,2-trifluoro-N-[(5S,6R,9R)-5-methoxy-3,6,9-trimethyl-2-oxo-8-(3,3,3-trifluoropropyl)-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]ethanesulfonamide
2-[(2R,4aS,12aR)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
N-[[(4S,5R)-2-[(2R)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4S,5S)-2-[(2R)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4S,5R)-2-[(2S)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4R,5S)-2-[(2R)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
N-[[(4R,5S)-2-[(2S)-1-hydroxypropan-2-yl]-8-[2-(4-methoxyphenyl)ethynyl]-4-methyl-1,1-dioxo-4,5-dihydro-3H-6,1$l^{6},2-benzoxathiazocin-5-yl]methyl]-N-methyl-2-pyridinecarboxamide
C30H33N3O6S (563.2089958000001)
2-[(2S,4aR,12aS)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
2-[(2S,4aR,12aR)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
2-[(2S,4aS,12aR)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
2-[(2S,4aS,12aS)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-[(4-phenylphenyl)methyl]acetamide
C30H33N3O6S (563.2089958000001)
[(1S)-7-methoxy-2-[(2-methoxyphenyl)methyl]-1-(4-methoxyphenyl)sulfonyl-1-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,3-azetidine]yl]methanol
C30H33N3O6S (563.2089958000001)
2-amino-4-({1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-{[2-hydroxy-3-(4-hydroxy-2-methoxyphenyl)-1-phenylpropyl]sulfanyl}ethyl}-C-hydroxycarbonimidoyl)butanoic acid
C26H33N3O9S (563.1937408000001)