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Cyclo(L-Pro-L-Tyr)

HCID 119404
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
4549-02-4
Standard SMILES
O=C1N[C@@H](Cc2ccc(O)cc2)C(=O)N2CCC[C@@H]12
InChIKey
LSGOTAXPWMCUCK-RYUDHWBXSA-N
Molecular formula
C14H16N2O3
Average molar mass
260.29 g/mol
Monoisotopic mass
260.11609237

Overview

Maculosin is a homodetic cyclic peptide that is a dipeptide composed of L-proline and L-tyrosine joined by peptide linkages. It has a role as a metabolite. It is a homodetic cyclic peptide, a member of phenols, a dipeptide and a pyrrolopyrazine. It is functionally related to a L-proline and a L-tyrosine.

Names & identifiers

Preferred name
Cyclo(L-Pro-L-Tyr)
IUPAC
(3S,8aS)-3-[(4-hydroxyphenyl)methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione
English name
MACULOSIN
Molecular formula
C14H16N2O3
Molecular weight
260.29

Names & synonyms

MaculosinCyclo(L-pro-L-tyr)4549-02-4DTXSID30196526(3S,8aS)-3-[(4-hydroxyphenyl)methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dioneCHEBI:6631(3S,8aS)-3-((4-hydroxyphenyl)methyl)-2,3,6,7,8,8a-hexahydropyrrolo(1,2-a)pyrazine-1,4-dioneRefChem:800441DTXCID70119017Cyclo(-Pro-Tyr)(3s,8as)-3-(4-hydroxybenzyl)hexahydropyrrolo[1,2-a]pyrazine-1,4-dioneCYCLO-(L-TYROSINE-L-PROLINE) INHIBITOR
Show more names
A-19C0/4/49ML-1532IIMaculosin TFAAntibiotic A-19CCyclo(L-Tyr-L-Pro-)MACULOSIN USP/EP/BP
Cyclo(L-prolinyl-L-tyrosine)(3S,8aS)-Hexahydro-3-[(4-hydroxyphenyl)methyl]pyrrolo[1,2-a]pyrazine-1,4-dione(3S,8AR)-3-(4-HYDROXYBENZYL)HEXAHYDROPYRROLO[1,2-A]PYRAZINE-1,4-DIONEcyclo(pro-tyr)MFCD030934671w1yCyclo-(L-Pro-L-Tyr)CHEMBL359788

Database identifiers

Properties

Computed structural propertiesFilling in

XLogP
1
Topological polar surface area
69.6 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
3
Rotatable bonds
2
Heavy atoms
19
Formal charge
0
Complexity
377

Experimental & physicochemical properties

DrugsPharmaceuticals -> Listed in ZINC15

Physicochemical properties

Melting point
156 · 156-159 °C
Boiling point
581.4 · 581.4±43.0 °C(Predicted)
Density
1.36 · 1.36±0.1 g/cm3(Predicted)
storage temp.
-15 °C · -15°C
solubility
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
form
A solid
pka
9.92 · 9.92±0.15(Predicted)
color
White to off-white
Symbol(GHS)
8 · GHS08,GHS06
Signal word
Danger
Hazard statements
301 · H301-H311-H331-H371
Precautionary statements
280 · P280-P302+P352-P312-P322-P361-P363-P405-P501-P260-P264-P270-P309+P311-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Danger

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

P260, P261, P262, P264, P270, P271, P280, P301+P316, P302+P352, P304+P340, P308+P316, P316, P321, P330, P361+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Hazard information

Hazard Classes and CategoriesAcute Tox. 3 (100%)

Safety data

Signal word
Danger
Symbol(GHS)
GHS08,GHS06
Hazard statements
H301-H311-H331-H371
Precautionary statements
P280-P302+P352-P312-P322-P361-P363-P405-P501-P260-P264-P270-P309+P311-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501

Chemistry & industry

Applications · 3 items

DescriptionMaculosin is a diketopiperazine metabolite produced by A. alternata, L. capsici, Streptomyces, and the Gram-negative, nonobligate predator bacterial strain 679-2. It acts as a host-specific phytotoxin, inducing formation of weeping necrotic lesions in leaves of spotted knapweed (C. maculosa) when used at a concentration of 10 μM. Maculosin reduces the growth of the plant pathogenic bacteria X. axonopodis and R. solanacearum (MICs = 31.25 μg/ml) as well as the pathogenic oomycetes P. cactorum, P. capsici, P. cinnamomi, P. infestans, and P. ultimum when used at concentrations ranging from 10 to 100 mg/ml. Maculosin also inhibits the growth of M. luteus, M. smegmatis, S. cerevisiae, C. albicans, C. neoformans, and A. niger when used in combination with pyrrolnitrin or banegasin.

UsesCyclo(L-Pro-L-Tyr) (maculosin) is a diketopiperazine formed by the fusion of tyrosine and proline, reported as a secondary metabolite of fungi and bacteria. In Pseudomonas aeruginosa, cyclo(L-Pro-L-Tyr) is capable of activating N-acylhomoserine lactones (AHLs). Cyclo(L-Pro-L-Tyr) is also capable of activating or antagonizing other LuxR-based quorum-sensing systems. While the mode of action of cyclo(L-Pro-L-Tyr) is not known, its activity suggests the existence of cross talk among bacterial signalling systems. Cyclo(L-Pro-L-Tyr) was identified as a host-specific toxin produced by Alternaria alternata on spotted knapweed.

UsesCyclo(L-prolinyl-L-tyrosine) is a diketopiperazine derivative isolated from Bacillus thuringiensis and Bacillus endophyticus.

Additional notes

DefinitionChEBI: A homodetic cyclic peptide that is a dipeptide composed of L-proline and L-tyrosine joined by peptide linkages.

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
CAS
4549-02-4
PubChem CID
119404
DTXSID
DTXSID30196526
ChEMBL
CHEMBL359788
ChEBI
CHEBI:6631
EC Number
686-487-6
Nikkaji
J92.068A