Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB02894"
| Predicate | Value (sorted: default) |
|---|---|
| rdfs:label |
"Sulfamic Acid 2,3-O-(1-Methylethylidene)-4,5-O-Sulfonyl-Beta-Fructopyranose Ester"
|
| rdf:type | |
| drugbank:description |
"
experimental
This compound belongs to the dioxolopyrans. These are compounds containing a dioxolopyran moiety, which consistts of a dioxole ring fused to a pyran ring.
Dioxolopyrans
Organic Compounds
Heterocyclic Compounds
Dioxolopyrans
Sulfuric Acid Diesters
Oxanes
Sulfuric Acid Amide Esters
1,3-Dioxolanes
Acetals
Polyamines
sulfuric acid diester
sulfuric acid amide ester
oxane
sulfuric acid derivative
meta-dioxolane
ether
acetal
polyamine
logP
-0.51
ALOGPS
logS
-1.6
ALOGPS
Water Solubility
1.01e+01 g/l
ALOGPS
logP
-0.62
ChemAxon
IUPAC Name
[(1S,2R,6S,9S)-11,11-dimethyl-4,4-dioxo-3,5,8,10,12-pentaoxa-4$l^{6}-thiatricyclo[7.3.0.0^{2,6}]dodecan-9-yl]methyl sulfamate
ChemAxon
Traditional IUPAC Name
[(1S,2R,6S,9S)-11,11-dimethyl-4,4-dioxo-3,5,8,10,12-pentaoxa-4$l^{6}-thiatricyclo[7.3.0.0^{2,6}]dodecan-9-yl]methyl sulfamate
ChemAxon
Molecular Weight
361.346
ChemAxon
Monoisotopic Weight
361.013737085
ChemAxon
SMILES
CC1(C)O[C@H]2[C@H]3OS(=O)(=O)O[C@H]3CO[C@@]2(COS(N)(=O)=O)O1
ChemAxon
Molecular Formula
C9H15NO10S2
ChemAxon
InChI
InChI=1S/C9H15NO10S2/c1-8(2)17-7-6-5(18-22(13,14)19-6)3-15-9(7,20-8)4-16-21(10,11)12/h5-7H,3-4H2,1-2H3,(H2,10,11,12)/t5-,6-,7-,9-/m0/s1
ChemAxon
InChIKey
InChIKey=GGOAQSGCBDRTHT-AZRUVXNYSA-N
ChemAxon
Polar Surface Area (PSA)
149.68
ChemAxon
Refractivity
66.31
ChemAxon
Polarizability
30.73
ChemAxon
Rotatable Bond Count
3
ChemAxon
H Bond Acceptor Count
8
ChemAxon
H Bond Donor Count
1
ChemAxon
pKa (strongest acidic)
11.09
ChemAxon
pKa (strongest basic)
-4
ChemAxon
Physiological Charge
0
ChemAxon
Number of Rings
3
ChemAxon
Bioavailability
1
ChemAxon
Rule of Five
true
ChemAxon
PubChem Compound
46936520
PubChem Substance
46507400
BindingDB
13057
PDB
SMS
BE0000322
Carbonic anhydrase 2
Human
# Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284
# Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423
unknown
Carbonic anhydrase 2
Inorganic ion transport and metabolism
Reversible hydration of carbon dioxide
CA2
8q22
Cytoplasm
None
7.47
29115.0
Human
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1373
GenAtlas
CA2
GeneCards
CA2
GenBank Gene Database
M77181
GenBank Protein Database
179780
UniProtKB
P00918
UniProt Accession
CAH2_HUMAN
CA-II
Carbonate dehydratase II
Carbonic anhydrase C
Carbonic anhydrase II
EC 4.2.1.1
>Carbonic anhydrase 2
SHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRILN
NGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHLV
HWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDPR
GLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELMV
DNWRPAQPLKNRQIKASFK
>783 bp
ATGTCCCATCACTGGGGGTACGGCAAACACAACGGACCTGAGCACTGGCATAAGGACTTC
CCCATTGCCAAGGGAGAGCGCCAGTCCCCTGTTGACATCGACACTCATACAGCCAAGTAT
GACCCTTCCCTGAAGCCCCTGTCTGTTTCCTATGATCAAGCAACTTCCCTGAGGATCCTC
AACAATGGTCATGCTTTCAACGTGGAGTTTGATGACTCTCAGGACAAAGCAGTGCTCAAG
GGAGGACCCCTGGATGGCACTTACAGATTGATTCAGTTTCACTTTCACTGGGGTTCACTT
GATGGACAAGGTTCAGAGCATACTGTGGATAAAAAGAAATATGCTGCAGAACTTCACTTG
GTTCACTGGAACACCAAATATGGGGATTTTGGGAAAGCTGTGCAGCAACCTGATGGACTG
GCCGTTCTAGGTATTTTTTTGAAGGTTGGCAGCGCTAAACCGGGCCTTCAGAAAGTTGTT
GATGTGCTGGATTCCATTAAAACAAAGGGCAAGAGTGCTGACTTCACTAACTTCGATCCT
CGTGGCCTCCTTCCTGAATCCTTGGATTACTGGACCTACCCAGGCTCACTGACCACCCCT
CCTCTTCTGGAATGTGTGACCTGGATTGTGCTCAAGGAACCCATCAGCGTCAGCAGCGAG
CAGGTGTTGAAATTCCGTAAACTTAACTTCAATGGGGAGGGTGAACCCGAAGAACTGATG
GTGGACAACTGGCGCCCAGCTCAGCCACTGAAGAACAGGCAAATCAAAGCTTCCTTCAAA
TAA
PF00194
Carb_anhydrase
function
carbon-oxygen lyase activity
function
binding
function
hydro-lyase activity
function
carbonate dehydratase activity
function
catalytic activity
function
lyase activity
function
ion binding
function
cation binding
function
transition metal ion binding
function
zinc ion binding
process
physiological process
process
one-carbon compound metabolism
process
metabolism
process
cellular metabolism
"
|
| owl:sameAs |
All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines3/drugbank_small.nt
The resource does not appear as an object