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Tavaborole

CAS No.
174671-46-6
Chemical Name:
Tavaborole
Synonyms
Kerydin;AN-269;AN 2690;CS-1054;avaborole;Tavaborole;Tavalborole;Tavaborole (USAN);Tavaborole (>90%);Tavaborole(AN-2690)
CBNumber:
CB42454906
Molecular Formula:
C7H6BFO2
Molecular Weight:
151.93
MDL Number:
MFCD10699483
MOL File:
174671-46-6.mol
MSDS File:
SDS
Last updated:2023-06-08 09:02:52

Tavaborole Properties

Melting point 120-122℃
Boiling point 230.8±50.0 °C(Predicted)
Density 1.28±0.1 g/cm3(Predicted)
storage temp. -20°C
solubility DMSO (Slightly), Methanol (Slightly)
pka 6.81±0.20(Predicted)
form powder
color white to beige
Stability Hygroscopic
FDA UNII K124A4EUQ3
ATC code D01AE24

SAFETY

Risk and Safety Statements

Tavaborole price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1227 Tavaborole ≥95% (HPLC) 174671-46-6 10MG $115 2023-06-20 Buy
Sigma-Aldrich SML1227 Tavaborole ≥95% (HPLC) 174671-46-6 50MG $451 2023-06-20 Buy
TCI Chemical T3775 Tavaborole 174671-46-6 250MG $257 2024-03-01 Buy
Cayman Chemical 23101 AN-2690 ≥98% 174671-46-6 1g $97 2024-03-01 Buy
Cayman Chemical 23101 AN-2690 ≥98% 174671-46-6 5g $360 2024-03-01 Buy
Product number Packaging Price Buy
SML1227 10MG $115 Buy
SML1227 50MG $451 Buy
T3775 250MG $257 Buy
23101 1g $97 Buy
23101 5g $360 Buy

Tavaborole Chemical Properties,Uses,Production

Description

Tavaborole (Kerydin®), discovered and developed by Anacor, was approved by the US FDA in July 2014. Tavaborole, topical solution, 5% is an oxaborole antifungal indicated for the treatment of onychomycosis of the toenails due to Trichophyton rubrum or Trichophyton mentagrophytes. The mechanism of action of tavaborole is inhibition of fungal protein synthesis, which inhibits an aminoacyl-transfer ribonucleic acid synthetase.

Uses

Tavaborole is a topical treatment of toenail onychomycosis.

Definition

ChEBI: A member of the class of benzoxaboroles that is 1,3-dihydro-1-hydroxy-2,1-benzoxaborole substituted at position 5 by a fluoro group. A topical antifungal agent used for the treatment of onychomycosis (fungal infection of the toenails and fingernails).

General Description

Tavaborole is a boron-based pharmaceutical agent. It has broad-spectrum oxaborole antifungal activity. Due to its low molecular weight, it facilitates maximal nail plate penetration than its predecessors.

Biochem/physiol Actions

Tavaborole (AN2690) is a potent antifungal that targets the post-transfer editing site of leucyl-tRNA synthetase (LeuRS). Tavaborole forms a covalent adduct with the 3′ adenosine of tRNA(leu) at the editing site of fungal, but not bacterial LeuRS, locking the enzyme in an inactive conformation. Tavaborole was recently approved for the treatment of onychomycosis of the toenail in adults.

Synthesis

Three syntheses of tavaborole (XXXII) have been reported. The 26.9 g scale approach started with 2-bromo-5-fluorophenyl methanol (257), which was treated with ethyl vinyl ether (258) to produce o-bromobenzyl alcohol derivative 259 in 82% yield. 259 was then converted into the corresponding phenylboronic acid, followed by the one-pot deprotection and spontaneous cyclization upon treatment with 6 M hydrochloric acid, delivering tavaborole (XXXII) in 43% yield.

Synthesis_174671-46-6

in vitro

an2690 showed the most active against fungi and especially against the dermatophytes t. rubrum and t. mentagrophytes, the primary fungal pathogens causing onychomycosis. in addition, an2690 was identified as having a unique profile of in vitro antidermatophyte activity, maintenance of this activity in the presence of keratin, and exceedingly good penetration of human nails [1].

target

Trichophyton species

References

[1] baker sj, zhang yk, akama t, lau a, zhou h, hernandez v, mao w, alley mr, sanders v, plattner jj. discovery of a new boron-containing antifungal agent, 5-fluoro-1,3-dihydro-1-hydroxy-2,1- benzoxaborole (an2690), for the potential treatment of onychomycosis. j med chem. 2006;49(15):4447-50.
[2] hui x, baker sj, wester rc, barbadillo s, cashmore ak, sanders v, hold km, akama t, zhang yk, plattner jj, maibach hi. in vitro penetration of a novel oxaborole antifungal (an2690) into the human nail plate. j pharm sci. 2007;96(10):2622-31.
[3] markham a. tavaborole: first global approval. drugs. 2014;74(13):1555-8.

1061223-45-7
174671-46-6
Synthesis of Tavaborole from (4-Fluoro-2-(hydroxyMethyl)phenyl)boronic acid
Global( 209)Suppliers
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View Lastest Price from Tavaborole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tavaborole pictures 2023-09-08 Tavaborole
174671-46-6
US $0.00 / KG Ton 1KG Ton 99%+ 2 tons/month Zhuhai Hairuide Bioscience and Technology Co., Ltd
Tavaborole pictures 2021-07-13 Tavaborole
174671-46-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
Tavaborole pictures 2021-07-09 Tavaborole
174671-46-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • Tavaborole pictures
  • Tavaborole
    174671-46-6
  • US $0.00 / KG Ton
  • 99%+
  • Zhuhai Hairuide Bioscience and Technology Co., Ltd
  • Tavaborole pictures
  • Tavaborole
    174671-46-6
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd
  • Tavaborole pictures
  • Tavaborole
    174671-46-6
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd

Tavaborole Spectrum

5-FLUOROBENZO[C][1,2]OXABOROL-1(3H)-OL AN 2690 AN-2690;TAVABOROLE;AN2690 Tavaborole 5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole 5-Fluoro-1,3-dihydro-2,1-benzoxaborol-1-ol AN-2690(Tavaborole) Tavaborole(AN-2690) AN-269 AN-2690;AN2690;AN 2690 5-Fluoro-1-hydroxyl-1,3-dihydrobenzo[c][1,2]oxaborole 5-Fluoro-1-hydroxy-2,1-benzoxaborolane TAVABOROLE; AN2690; AN 2690 avaborole CS-1054 Tavaborole (USAN) 1,3-Dihydro-5-fluoro-1-hydroxy-2,1-benzoxaborole 2,1-Benzoxaborole, 5-fluoro-1,3-dihydro-1-hydroxy- Tavaborole (>90%) 5-Fluoro-2,1-benzoxaborol-1(3H)-ol 5-fluoro-1-hydroxy-3H-2,1-benzoxaborole Tavalborole Kerydin 5-Fluorobenzo[c][1,2]oxaboro-1(3H)-ol 5-FLUOROBENZO[C][1,2]OXABOROL-1(3H)-OL 174671-46-6 5-Fluorobenzo[c][1,2]oxaborole-1(3H)-ol Tavaborole In-House 174671-46-6 174461-46-6