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2158-02-3 | morpholine-4-carboxamide
CAS No: 2158-02-3 Catalog No: AG00BV51 MDL No:MFCD00085717
Product Description
Catalog Number:
AG00BV51
Chemical Name:
morpholine-4-carboxamide
CAS Number:
2158-02-3
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
MDL Number:
MFCD00085717
IUPAC Name:
morpholine-4-carboxamide
InChI:
InChI=1S/C5H10N2O2/c6-5(8)7-1-3-9-4-2-7/h1-4H2,(H2,6,8)
InChI Key:
ZKWFSTHEYLJLEL-UHFFFAOYSA-N
SMILES:
NC(=O)N1CCOCC1
EC Number:
218-474-4
NSC Number:
10542
Properties
Complexity:
110
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
130.074g/mol
Formal Charge:
0
Heavy Atom Count:
9
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
130.147g/mol
Monoisotopic Mass:
130.074g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
55.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.2
Literature
| Title | Journal |
|---|---|
| Synthesis, antitumor, antitrypanosomal and antileishmanial activities of benzo[4,5]canthin-6-ones bearing the N'-(Substituted benzylidene)-carbohydrazide and N-Alkylcarboxamide groups at C-2. | Chemical & pharmaceutical bulletin 20120101 |
| Asymmetric synthesis of (+)-galbelgin, (-)-kadangustin J, (-)-cyclogalgravin and (-)-pycnanthulignenes A and B, three structurally distinct lignan classes, using a common chiral precursor. | The Journal of organic chemistry 20110819 |
| New classes of alanine racemase inhibitors identified by high-throughput screening show antimicrobial activity against Mycobacterium tuberculosis. | PloS one 20110101 |
| Modeling of human prokineticin receptors: interactions with novel small-molecule binders and potential off-target drugs. | PloS one 20110101 |
| The oxytocin-oxytocin receptor system and its antagonists as tocolytic agents. | International journal of endocrinology 20110101 |
| Structural insights into substrate specificity in variants of N-acetylneuraminic Acid lyase produced by directed evolution. | Journal of molecular biology 20101119 |
| In vitro metabolism of indomethacin morpholinylamide (BML-190), an inverse agonist for the peripheral cannabinoid receptor (CB(2)) in rat liver microsomes. | European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 20100911 |
| BML-111, a lipoxin receptor agonist, modulates the immune response and reduces the severity of collagen-induced arthritis. | Inflammation research : official journal of the European Histamine Research Society ... [et al.] 20080401 |
| Lewis base activation of Lewis acids: catalytic, enantioselective vinylogous aldol addition reactions. | The Journal of organic chemistry 20070720 |
| Cannabinoids stimulate fibroblastic colony formation by bone marrow cells indirectly via CB2 receptors. | Calcified tissue international 20070101 |
| Lewis base activation of Lewis acids. Vinylogous aldol addition reactions of conjugated N,O-silyl ketene acetals to aldehydes. | Journal of the American Chemical Society 20060201 |
| Syntheses and neuraminidase inhibitory activity of multisubstituted cyclopentane amide derivatives. | Journal of medicinal chemistry 20040408 |
| Reduction of human monocytic cell neurotoxicity and cytokine secretion by ligands of the cannabinoid-type CB2 receptor. | British journal of pharmacology 20030601 |
| BML-190 and AM251 act as inverse agonists at the human cannabinoid CB2 receptor: signalling via cAMP and inositol phosphates. | FEBS letters 20030211 |
| Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor alpha release in vitro and in vivo. | Journal of medicinal chemistry 20010802 |
| Effects of cannabinoids on LPS-stimulated inflammatory mediator release from macrophages: involvement of eicosanoids. | Journal of cellular biochemistry 20010101 |
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