Telbivudine - ≥98% , DNA polymerase/reverse transcriptase inhibitor, CAS No.3424-98-4, DNA polymerase/reverse transcriptase inhibitor

CAS: 3424-98-4 Cat. No.: T129668 Formule: C₁₀H₁₄N₂O₅ Poids moléculaire: 242.23 Numéro CE: 608-961-3

QUALITÉ & PURETÉ ≥98%

Synonyms

BP-58605 | DB01265 | Epavudine;L-Thymidine;NV 02B | Telbivudine (Sebivo, Tyzeka) | beta-L-Thymidine | Tyzeka | AC-5632 | AS-35209 | beta-L-2'-Deoxythymidine | Telbivudina | TELBIVUDINE (MART.) | CHEBI:63624 | NB 02B | Telbivudine (USAN/INN) | 1-(2-Deoxy-b

Storage

Store at 2-8°C

Shipped In

Wet ice

Vue d’ensemble

Telbivudine is a potent, and selective HBV reverse transcriptase inhibitor, used to treat HBV infection.
A specific hepatitis B virus (HBV) replication inhibitor

Spécifications

Synonymes

BP-58605 | DB01265 | Epavudine;L-Thymidine;NV 02B | Telbivudine (Sebivo, Tyzeka) | beta-L-Thymidine | Tyzeka | AC-5632 | AS-35209 | beta-L-2'-Deoxythymidine | Telbivudina | TELBIVUDINE (MART.) | CHEBI:63624 | NB 02B | Telbivudine (USAN/INN) | 1-(2-Deoxy-b

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

Telbivudine is a nucleoside analog. A specific inhibitor of hepatitis B virus (HBV) replication. Antiviral.Antiviral agent. Thymidine analog. Shows immunomodulatory effects. Suppresses programmed death ligand 1 expression on T cells. Orally active. Potent

Conditions de stockage de stockage

Store at 2-8°C

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Mécanisme d'action

DNA polymerase/reverse transcriptase inhibitor

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureté

≥98%

Propriétés du produit

ALogP

-1.2

Noms et identifiants

Pubchem Sid

488188284

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488188284

Sourires canoniques

CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O

IUPAC Name

1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

InChIKey

IQFYYKKMVGJFEH-CSMHCCOUSA-N

INCHI

1S/C10H14N2O5/c1-5-3-12(10(16)11-9(5)15)8-2-6(14)7(4-13)17-8/h3,6-8,13-14H,2,4H2,1H3,(H,11,15,16)/t6-,7+,8+/m1/s1

Isomères SMILES

CC1=CN(C(=O)NC1=O)[C@@H]2C[C@H]([C@@H](O2)CO)O

WGK Allemagne

3

RTECS

UV9048500

Poids moléculaire

242.23

Reaxy-Rn

889638

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=889638&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Classe Pyrimidine nucleosides
      • Subclass Pyrimidine 2'-deoxyribonucleosides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Classe: Pyrimidine nucleosides
• Subclass: Pyrimidine 2'-deoxyribonucleosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine 2'-deoxyribonucleosides
• Alternative Parents: Pyrimidones Hydropyrimidines Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Ureas Secondary alcohols Lactams Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidine 2'-deoxyribonucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Tetrahydrofuran - Vinylogous amide - Lactam - Secondary alcohol - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.
• External Descriptors: pyrimidine 2'-deoxyribonucleoside

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water (48 mg/ml at 25 °C), DMSO (48 mg/ml at 25 °C), and ethanol (2 mg/ml at 25 °C)
• Poids moléculaire: 242.230 g/mol
• XLogP3: -1.200
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 242.09 Da
• Monoisotopic Mass: 242.09 Da
• Topological Polar Surface Area: 99.100 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 381.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1