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Molecule
ID:133654
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₃BrN₂O₅
Molecular Mass
333.13532
Exact Mass
332.00078353
Charge
0
InChI
InChI=1S/C11H13BrN2O5/c12-2-1-6-4-14(11(18)13-10(6)17)9-3-7(16)8(5-15)19-9/h1-2,4,7-9,15-16H,3,5H2,(H,13,17,18)/b2-1-/t7-,8?,9+/m0/s1
InChIKey
ODZBBRURCPAEIQ-LVHJSNLWSA-N
Canonic Smiles
Br/C=C\c1cn([C@H]2C[C@@H](C(O2)CO)O)c(=O)[nH]c1=O
Isomeric Smiles
c1c(c(=O)[nH]c(=O)n1[C@H]1C[C@@H](C(O1)CO)O)/C=C\Br
Calculated Properties
JChem
Acid pKa
9.341513
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-0.49662927
LogD (pH = 7.4)
-0.5014516
Log P
-0.49656743
Molar Refractivity
67.6767
Polarizability
26.512186
Polar Surface Area
99.1
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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IUPAC name
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IUPAC Traditional name
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MDL Number
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PubChem SID
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CAS Number
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PubChem CID
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
16219063
Commercial Catalog
Sigma Aldrich
B9647
Names and Identifiers
Synonyms
(E)-5-(2-Bromovinyl)-2′-deoxyuridine
BVdU
IUPAC name
5-[(Z)-2-bromoethenyl]-1-[(2R,4S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione
IUPAC Traditional name
5-[(Z)-2-bromoethenyl]-1-[(2R,4S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-pyrimidine-2,4-dione
Registration numbers
MDL Number
MFCD00058585
PubChem SID
24278280
162227931
CAS Number
69304-47-8
PubChem CID
16219063
Properties
Safety Information
Storage Temperature
2-8°C
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
RTECS
YU7355000
Source
German water hazard class
3
Source
Pharmacology Properties
Gene Information
human ... HV1S(3365)
Source
Molecule Details
Sigma Aldrich
B9647
Biochem/physiol Actions
An exceptionally potent inhibitor of Herpes simplex virus type 1.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay