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102849-12-7 | L-Lysine,N2-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-
CAS No: 102849-12-7 Catalog No: AG01CC6Z MDL No:MFCD16661254
Product Description
Catalog Number:
AG01CC6Z
Chemical Name:
L-Lysine,N2-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-
CAS Number:
102849-12-7
Molecular Formula:
C23H33N5O7S
Molecular Weight:
523.6024
MDL Number:
MFCD16661254
IUPAC Name:
(2S)-6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-2-[3-(2,5-dioxopyrrol-1-yl)propanoylamino]hexanoic acid
InChI:
InChI=1S/C23H33N5O7S/c29-17(7-2-1-6-16-21-15(13-36-16)26-23(35)27-21)24-11-4-3-5-14(22(33)34)25-18(30)10-12-28-19(31)8-9-20(28)32/h8-9,14-16,21H,1-7,10-13H2,(H,24,29)(H,25,30)(H,33,34)(H2,26,27,35)/t14-,15-,16-,21-/m0/s1
InChI Key:
KWNGAZCDAJSVLC-OSAWLIQMSA-N
SMILES:
O=C(CCCC[C@@H]1SC[C@H]2[C@@H]1NC(=O)N2)NCCCC[C@@H](C(=O)O)NC(=O)CCN1C(=O)C=CC1=O
Properties
Complexity:
893
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
4
Defined Bond Stereocenter Count:
0
Exact Mass:
523.21g/mol
Formal Charge:
0
Heavy Atom Count:
36
Hydrogen Bond Acceptor Count:
8
Hydrogen Bond Donor Count:
5
Isotope Atom Count:
0
Molecular Weight:
523.605g/mol
Monoisotopic Mass:
523.21g/mol
Rotatable Bond Count:
15
Topological Polar Surface Area:
199A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7
Literature
| Title | Journal |
|---|---|
| Effect of oxybutynin and imidafenacin on central muscarinic receptor occupancy and cognitive function: a monkey PET study with [(11)C](+)3-MPB. | NeuroImage 20110901 |
| Validation of reference tissue model of PET ligand [¹¹C]+3-MPB for the muscarinic cholinergic receptor in the living brain of conscious monkey. | Synapse (New York, N.Y.) 20110601 |
| Muscarinic receptor occupancy and cognitive impairment: a PET study with [11C](+)3-MPB and scopolamine in conscious monkeys. | Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20110601 |
| Thiols in the alphaIIbbeta3 integrin are necessary for platelet aggregation. | British journal of haematology 20080701 |
| Chemical modification of mono-cysteine mutants allows a more global look at conformations of the epsilon subunit of the ATP synthase from Escherichia coli. | Journal of bioenergetics and biomembranes 20070201 |
| Redox control of changes in protein sulfhydryl levels during human sperm capacitation. | Free radical biology & medicine 20031115 |
| Regulation of protein tyrosine phosphatase 1B in intact cells by S-nitrosothiols. | Archives of biochemistry and biophysics 20030215 |
| Helix packing in subunit a of the Escherichia coli ATP synthase as determined by chemical labeling and proteolysis of the cysteine-substituted protein. | Biochemistry 20030121 |
| Disulfide exchange in domain 2 of CD4 is required for entry of HIV-1. | Nature immunology 20020801 |
| Characterization of redox-active proteins on cell surface. | Methods in enzymology 20020101 |
| Measurement of reduction of disulfide bonds in plasmin by phosphoglycerate kinase. | Methods in enzymology 20020101 |
| PET imaging of ischemic neuronal death in the hippocampus of living monkeys. | Hippocampus 20020101 |
| Identification of redox-active proteins on cell surface. | Methods in enzymology 20020101 |
| Cryopreservation alters membrane sulfhydryl status of bull spermatozoa: protection by oxidized glutathione. | Molecular reproduction and development 20011201 |
| Protein disulfide isomerase and sulfhydryl-dependent pathways in platelet activation. | Biochemistry 20010522 |
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