Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB07543"
Predicate | Value (sorted: default) |
---|---|
rdfs:label |
"(2S)-1-(9H-Carbazol-4-yloxy)-3-(isopropylamino)propan-2-ol"
|
rdf:type | |
drugbank:description |
"
experimental
This compound belongs to the carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
Carbazoles
Organic Compounds
Heterocyclic Compounds
Indoles and Derivatives
Carbazoles
Indoles
Phenol Ethers
Alkyl Aryl Ethers
Pyrroles
Secondary Alcohols
1,2-Aminoalcohols
Polyamines
Dialkylamines
indole
phenol ether
alkyl aryl ether
benzene
pyrrole
1,2-aminoalcohol
secondary alcohol
secondary amine
polyamine
ether
secondary aliphatic amine
amine
alcohol
organonitrogen compound
logP
3.12
ALOGPS
logS
-4
ALOGPS
Water Solubility
3.10e-02 g/l
ALOGPS
logP
2.71
ChemAxon
IUPAC Name
[(2S)-3-(9H-carbazol-4-yloxy)-2-hydroxypropyl](propan-2-yl)amine
ChemAxon
Traditional IUPAC Name
[(2S)-3-(9H-carbazol-4-yloxy)-2-hydroxypropyl](isopropyl)amine
ChemAxon
Molecular Weight
298.3795
ChemAxon
Monoisotopic Weight
298.168127958
ChemAxon
SMILES
[H][C@](O)(CNC(C)C)COC1=CC=CC2=C1C1=C(N2)C=CC=C1
ChemAxon
Molecular Formula
C18H22N2O2
ChemAxon
InChI
InChI=1S/C18H22N2O2/c1-12(2)19-10-13(21)11-22-17-9-5-8-16-18(17)14-6-3-4-7-15(14)20-16/h3-9,12-13,19-21H,10-11H2,1-2H3/t13-/m0/s1
ChemAxon
InChIKey
InChIKey=BQXQGZPYHWWCEB-ZDUSSCGKSA-N
ChemAxon
Polar Surface Area (PSA)
57.28
ChemAxon
Refractivity
87.79
ChemAxon
Polarizability
34.14
ChemAxon
Rotatable Bond Count
6
ChemAxon
H Bond Acceptor Count
3
ChemAxon
H Bond Donor Count
3
ChemAxon
pKa (strongest acidic)
14.03
ChemAxon
pKa (strongest basic)
9.67
ChemAxon
Physiological Charge
1
ChemAxon
Number of Rings
3
ChemAxon
Bioavailability
1
ChemAxon
Rule of Five
true
ChemAxon
Ghose Filter
true
ChemAxon
MDDR-Like Rule
true
ChemAxon
PubChem Compound
13023332
PubChem Substance
99444014
PDB
CAU
BE0001248
Lysozyme
Enterobacteria phage T4
# Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/10592235
unknown
Lysozyme
Involved in lysozyme activity
Helps to release the mature phage particles from the cell wall by breaking down the peptidoglycan
E
Cytoplasmic
None
10.08
18636.0
Enterobacteria phage T4
GenBank Gene Database
X04567
GenBank Protein Database
15261
UniProtKB
P00720
UniProt Accession
LYS_BPT4
EC 3.2.1.17
Endolysin
Lysis protein
Muramidase
>Lysozyme
MNIFEMLRIDEGLRLKIYKDTEGYYTIGIGHLLTKSPSLNAAKSELDKAIGRNCNGVITK
DEAEKLFNQDVDAAVRGILRNAKLKPVYDSLDAVRRCALINMVFQMGETGVAGFTNSLRM
LQQKRWDEAAVNLAKSRWYNQTPNRAKRVITTFRTGTWDAYKNL
>495 bp
ATGAATATATTTGAAATGTTACGTATAGATGAACGTCTTAGACTTAAAATCTATAAAGAC
ACAGAAGGCTATTACACTATTGGCATCGGTCATTTGCTTACAAAAAGTCCATCACTTAAT
GCTGCTAAATCTGAATTAGATAAAGCTATTGGGCGTAATTGCAATGGTGTAATTACAAAA
GATGAGGCTGAAAAACTCTTTAATCAGGATGTTGATGCTGCTGTTCGCGGAATTCTGAGA
AATGCTAAATTAAAACCGGTTTATGATTCTCTTGATGCGGTTCGTCGCTGTGCATTGATT
AATATGGTTTTCCAAATGGGAGAAACCGGTGTGGCAGGATTTACTAACTCTTTACGTATG
CTTCAACAAAAACGCTGGGATGAAGCAGCAGTTAACTTAGCTAAAAGTATATGGTATAAT
CAAACACCTAATCGCGCAAAACGAGTCATTACAACGTTTAGAACTGGCACTTGGGACGCG
TATAAAAATCTATAA
PF00959
Phage_lysozyme
function
hydrolase activity, acting on glycosyl bonds
function
hydrolase activity, hydrolyzing O-glycosyl compounds
function
lysozyme activity
function
catalytic activity
function
hydrolase activity
process
physiological process
process
catabolism
process
cellular catabolism
process
metabolism
process
cell wall catabolism
process
peptidoglycan catabolism
process
macromolecule metabolism
process
carbohydrate metabolism
process
cellular carbohydrate metabolism
process
peptidoglycan metabolism
BE0000694
Beta-2 adrenergic receptor
Human
# Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/10592235
unknown
Beta-2 adrenergic receptor
Involved in beta2-adrenergic receptor activity
Beta-adrenergic receptors mediate the catecholamine- induced activation of adenylate cyclase through the action of G proteins. The beta-2-adrenergic receptor binds epinephrine with an approximately 30-fold greater affinity than it does norepinephrine
ADRB2
5q31-q32
Membrane; multi-pass membrane protein
35-58
72-95
107-129
151-174
197-220
275-298
306-329
7.44
46557.0
Human
HUGO Gene Nomenclature Committee (HGNC)
HGNC:286
GenAtlas
ADRB2
GeneCards
ADRB2
GenBank Gene Database
Y00106
GenBank Protein Database
29371
IUPHAR
29
Guide to Pharmacology
4
UniProtKB
P07550
UniProt Accession
ADRB2_HUMAN
Beta-2 adrenoceptor
Beta-2 adrenoreceptor
>Beta-2 adrenergic receptor
MGQPGNGSAFLLAPNRSHAPDHDVTQQRDEVWVVGMGIVMSLIVLAIVFGNVLVITAIAK
FERLQTVTNYFITSLACADLVMGLAVVPFGAAHILMKMWTFGNFWCEFWTSIDVLCVTAS
IETLCVIAVDRYFAITSPFKYQSLLTKNKARVIILMVWIVSGLTSFLPIQMHWYRATHQE
AINCYANETCCDFFTNQAYAIASSIVSFYVPLVIMVFVYSRVFQEAKRQLQKIDKSEGRF
HVQNLSQVEQDGRTGHGLRRSSKFCLKEHKALKTLGIIMGTFTLCWLPFFIVNIVHVIQD
NLIRKEVYILLNWIGYVNSGFNPLIYCRSPDFRIAFQELLCLRRSSLKAYGNGYSSNGNT
GEQSGYHVEQEKENKLLCEDLPGTEDFVGHQGTVPSDNIDSQGRNCSTNDSLL
>1242 bp
ATGGGGCAACCCGGGAACGGCAGCGCCTTCTTGCTGGCACCCAATAGAAGCCATGCGCCG
GACCACGACGTCACGCAGCAAAGGGACGAGGTGTGGGTGGTGGGCATGGGCATCGTCATG
TCTCTCATCGTCCTGGCCATCGTGTTTGGCAATGTGCTGGTCATCACAGCCATTGCCAAG
TTCGAGCGTCTGCAGACGGTCACCAACTACTTCATCACTTCACTGGCCTGTGCTGATCTG
GTCATGGGCCTGGCAGTGGTGCCCTTTGGGGCCGCCCATATTCTTATGAAAATGTGGACT
TTTGGCAACTTCTGGTGCGAGTTTTGGACTTCCATTGATGTGCTGTGCGTCACGGCCAGC
ATTGAGACCCTGTGCGTGATCGCAGTGGATCGCTACTTTGCCATTACTTCACCTTTCAAG
TACCAGAGCCTGCTGACCAAGAATAAGGCCCGGGTGATCATTCTGATGGTGTGGATTGTG
TCAGGCCTTACCTCCTTCTTGCCCATTCAGATGCACTGGTACCGGGCCACCCACCAGGAA
GCCATCAACTGCTATGCCAATGAGACCTGCTGTGACTTCTTCACGAACCAAGCCTATGCC
ATTGCCTCTTCCATCGTGTCCTTCTACGTTCCCCTGGTGATCATGGTCTTCGTCTACTCC
AGGGTCTTTCAGGAGGCCAAAAGGCAGCTCCAGAAGATTGACAAATCTGAGGGCCGCTTC
CATGTCCAGAACCTTAGCCAGGTGGAGCAGGATGGGCGGACGGGGCATGGACTCCGCAGA
TCTTCCAAGTTCTGCTTGAAGGAGCACAAAGCCCTCAAGACGTTAGGCATCATCATGGGC
ACTTTCACCCTCTGCTGGCTGCCCTTCTTCATCGTTAACATTGTGCATGTGATCCAGGAT
AACCTCATCCGTAAGGAAGTTTACATCCTCCTAAATTGGATAGGCTATGTCAATTCTGGT
TTCAATCCCCTTATCTACTGCCGGAGCCCAGATTTCAGGATTGCCTTCCAGGAGCTTCTG
TGCCTGCGCAGGTCTTCTTTGAAGGCCTATGGGAATGGCTACTCCAGCAACGGCAACACA
GGGGAGCAGAGTGGATATCACGTGGAACAGGAGAAAGAAAATAAACTGCTGTGTGAAGAC
CTCCCAGGCACGGAAGACTTTGTGGGCCATCAAGGTACTGTGCCTAGCGATAACATTGAT
TCACAAGGGAGGAATTGTAGTACAAATGACTCACTGCTGTAA
PF00001
7tm_1
component
intrinsic to membrane
component
integral to membrane
component
membrane
component
cell
function
amine receptor activity
function
signal transducer activity
function
adrenoceptor activity
function
receptor activity
function
beta-adrenergic receptor activity
function
transmembrane receptor activity
function
beta2-adrenergic receptor activity
function
G-protein coupled receptor activity
function
rhodopsin-like receptor activity
process
cell surface receptor linked signal transduction
process
G-protein coupled receptor protein signaling pathway
process
cellular process
process
cell communication
process
signal transduction
"
|
All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines3/drugbank_small.nt
The resource does not appear as an object