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LY2940680

CAS No.
1258861-20-9
Chemical Name:
LY2940680
Synonyms
Taladegib;NSC7667;NSC 7667;NSC-7667;LY2940680;LY2940680 USP/EP/BP;LY2940680 (Taladegib);Taladegib (LY2940680);LY 2940680; LY2940680;Taladegib hydrochloride
CBNumber:
CB02516035
Molecular Formula:
C26H24F4N6O
Molecular Weight:
512.5
MDL Number:
MFCD21609264
MOL File:
1258861-20-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41
Product description Number Pack Size Price
LY2940680 ≥98% 16264 1mg $68
LY2940680 ≥98% 16264 5mg $179
LY2940680 ≥98% 16264 10mg $322
LY 2940680 FL103462 5mg $344.8
LY 2940680 FL103462 10mg $586.3
More product size

LY2940680 Properties

Boiling point 703.5±60.0 °C(Predicted)
Density 1.39
storage temp. Store at -20°C
solubility insoluble in H2O; ≥5.2 mg/mL in EtOH with ultrasonic; ≥51.3 mg/mL in DMSO with gentle warming and ultrasonic
form crystalline solid
pka 7.94±0.30(Predicted)
color White to off-white
FDA UNII QY8BWX1LJ5
NCI Drug Dictionary taladegib

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)
GHS08
Signal word  Danger
Hazard statements  H360-H373
Precautionary statements  P260-P314-P501
NFPA 704
0
2 0

LY2940680 price More Price(52)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 16264 LY2940680 ≥98% 1258861-20-9 1mg $68 2026-04-30 Buy
Cayman Chemical 16264 LY2940680 ≥98% 1258861-20-9 5mg $179 2026-04-30 Buy
Cayman Chemical 16264 LY2940680 ≥98% 1258861-20-9 10mg $322 2026-04-30 Buy
Biosynth FL103462 LY 2940680 1258861-20-9 5mg $344.8 2026-06-04 Buy
Biosynth FL103462 LY 2940680 1258861-20-9 10mg $586.3 2026-06-04 Buy
Product number Packaging Price Buy
16264 1mg $68 Buy
16264 5mg $179 Buy
16264 10mg $322 Buy
FL103462 5mg $344.8 Buy
FL103462 10mg $586.3 Buy

LY2940680 Chemical Properties,Uses,Production

Uses

Smoothened (Smo) is a GPCR-like receptor that, with Patched, mediates hedgehog (Hh) signaling to regulate gene expression through the Gli transcription factors. LY2940680 is an antitumor agent that binds to the human Smo receptor and inhibits Sonic Hh-induced Gli1 expression (IC50 = ~2.4 nM in vitro). The potential anticancer activity of LY2940680 is currently under clinical investigation.[Cayman Chemical]

Uses

LY2940680 binds to the Smoothened (Smo) receptor and potently inhibits Hedgehog (Hh) signaling.

Biological Activity

ly2940680 is a selective inhibitor of smo receptor and thus inhibits hh signaling pathway [1].smoothened(smo) receptor is a member of class f g protein-coupled receptors, which plays an important role in the main transducer of the hedgehog (hh) signaling pathway that implicated in a wide range of developmental and adult processes [2].ly2940680 is a potent smo receptor inhibitor that binds mostly to extracelluar loops and has a different functioning site with the reported smo receptor inhibitor sant-1 which binds to 7tm [2]. when tested with cell lines containing a mutation in the gene encoding smoothened that researchers had previously observed in patient with cancer who developed resistance to vismodegib, ly2940680 inhibited cell proliferation [3].many studies have shown that hh signaling pathway plays a pivotal role in cscs and hh inhibition caused many aspects of transformation attributed to cscs. in patients with basal cell carcinoma and medulloblastoma, ly2940680 showed good efficacy as a monotherapy [1].

Synthesis

4-Piperidinamine, N-methyl-1-[4-(1-methyl-1H-pyrazol-5-yl)-1-phthalazinyl]-

1258861-50-5

4-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE

189807-21-4

LY2940680

1258861-20-9

Example 14 - Procedure for the synthesis of N-fluoro-N-methyl-N-[1-[4-(1-methyl-1H-pyrazol-5-yl)-1-phthalazinyl]-4-piperidinyl]-2-(trifluoromethyl)benzamide: N-methyl-1-[4-(1-methyl-1H-pyrazol-5-yl)phthalazin-1-yl]piperidin-4-amine (2.8 g, 8.68 mmol) and triethylamine ( 3.36 mL, 26.1 mmol) were dissolved in dichloromethane (30 mL) and 4-fluoro-2-(trifluoromethyl)benzoyl chloride (2.14 mL, 10.42 mmol) was added. The reaction mixture was stirred at room temperature for 3 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure. The resulting residue was purified by fast silica gel chromatography with an eluent ratio of hexane:ethyl acetate:methanol solution of 2M NH3 = 20:5:1 to give the target product, free base, as a yellow foam (3.83 g, 86% yield). Mass spectral analysis showed ES/MS m/z 513.0 ([M+H]+).

target

Smoothened

References

[1]. justilien, v. and a.p. fields, molecular pathways: novel approaches for improved therapeutic targeting of hedgehog signaling in cancer stem cells. clin cancer res, 2015. 21(3): p. 505-13.
[2]. hoch, l., et al., mrt-92 inhibits hedgehog signaling by blocking overlapping binding sites in the transmembrane domain of the smoothened receptor. faseb j, 2015. 29(5): p. 1817-29.
[3]. redmond, e.m., et al., investigational notch and hedgehog inhibitors--therapies for cardiovascular disease. expert opin investig drugs, 2011. 20(12): p. 1649-64.

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View Lastest Price from LY2940680 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Taladegib pictures 2026-07-27 Taladegib
1258861-20-9
$56.00-151.00 99.80% 10g TargetMol Chemicals Inc.
LY2940680 pictures 2019-12-20 LY2940680
1258861-20-9
$1.00 1KG 99% 100kgs Career Henan Chemical Co
  • Taladegib pictures
  • Taladegib
    1258861-20-9
  • $56.00-151.00
  • 99.80%
  • TargetMol Chemicals Inc.
  • LY2940680 pictures
  • LY2940680
    1258861-20-9
  • $1.00
  • 99%
  • Career Henan Chemical Co

LY2940680 Spectrum

Taladegib (LY2940680) 4-Fluoro-N-methyl-N-[1-[4-(1-methyl-1H-pyrazol-5-yl)-1-phthalazinyl]-4-piperidinyl]-2-(trifluoromethyl)benzamide LY 2940680 LY2940680 LY2940680 (Taladegib) Taladegib hydrochloride 4-Fluoro-N-methyl-N-(1-(4-(1-methyl-1H-pyrazol-5-yl)phthalazin-1-yl)piperidin-4-yl)-2-(trifluo 4-Fluoro-N-methyl-N-[1-[4-(1-methyl-1H-pyrazol-5-yl)-1-phthalazinyl]-4-piperidinyl]-2-(trifluoromethyl)benzamide 4-fluoro-N-Methyl-N-(1-(4-(1-Methyl-1H-pyrazol-5-yl)phthalazin-1-yl)piperidin-4-yl)-2-(trifluoroMethyl)benzaMide 4-fluoro-N-Methyl-N-[1-[4-(2-Methylpyrazol-3-yl)phthalazin-1-yl]piperidin-4-yl]-2-(trifluoroMethyl)benzaMide LY 2940680; LY2940680 Benzamide, 4-fluoro-N-methyl-N-[1-[4-(1-methyl-1H-pyrazol-5-yl)-1-phthalazinyl]-4-piperidinyl]-2-(trifluoromethyl)- LY2940680 USP/EP/BP NSC 7667 NSC7667 NSC-7667 LY2940680 Taladegib LY-2940680 Taladegib (LY2940680) ,S2157 Taladegib 1258861-20-9 C26H24F4N6O Inhibitors