Sonidegib free base

Sonidegib free base 

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Sonidegib (diphosphate)

HY-16582 100mg
EUR 154.76
Description: Sonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectively[1].

Sonidegib diphosphate

T15727-10mg 10mg Ask for price
Description: Sonidegib diphosphate

Sonidegib diphosphate

T15727-1g 1g Ask for price
Description: Sonidegib diphosphate

Sonidegib diphosphate

T15727-1mg 1mg Ask for price
Description: Sonidegib diphosphate

Sonidegib diphosphate

T15727-50mg 50mg Ask for price
Description: Sonidegib diphosphate

Sonidegib diphosphate

T15727-5mg 5mg Ask for price
Description: Sonidegib diphosphate

Sonidegib (LDE-225)

205510 25.0mg
EUR 90

Sonidegib metabolite M48

HY-117229 Get quote Ask for price
Description: Sonidegib metabolite M48 is the main circulating metabolite of Sonidegib. Sonidegib is a hedgehog pathway inhibitor. M48 showed a much longer Tmax (60 h) than Sonidegib[1].

LDE225 (NVP-LDE225, Sonidegib)

MBS385025-100mg 100mg
EUR 345

LDE225 (NVP-LDE225, Sonidegib)

MBS385025-10mg 10mg
EUR 160

LDE225 (NVP-LDE225, Sonidegib)

MBS385025-1mLinDMSO 1mL(inDMSO)
EUR 140

LDE225 (NVP-LDE225, Sonidegib)

MBS385025-50mg 50mg
EUR 240

LDE225 (NVP-LDE225, Sonidegib)

MBS385025-5mg 5mg
EUR 140

Sonidegib Hydrazo Impurity-D8

ESS0501-5mg 5 mg
EUR 700

I-37 free base (2359690-13-2(free base))

MBS5759495-10mg 10mg
EUR 470

I-37 free base (2359690-13-2(free base))

MBS5759495-1mg 1mg
EUR 210

I-37 free base (2359690-13-2(free base))

MBS5759495-25mg 25mg
EUR 780

I-37 free base (2359690-13-2(free base))

MBS5759495-50mg 50mg
EUR 1130

I-37 free base (2359690-13-2(free base))

MBS5759495-5mg 5mg
EUR 335

I-37 free base( 2359690-13-2(free base))

T8721L-10mg 10mg Ask for price
Description: I-37 free base( 2359690-13-2(free base))

I-37 free base( 2359690-13-2(free base))

T8721L-1g 1g Ask for price
Description: I-37 free base( 2359690-13-2(free base))

I-37 free base( 2359690-13-2(free base))

T8721L-1mg 1mg Ask for price
Description: I-37 free base( 2359690-13-2(free base))

I-37 free base( 2359690-13-2(free base))

T8721L-50mg 50mg Ask for price
Description: I-37 free base( 2359690-13-2(free base))

I-37 free base( 2359690-13-2(free base))

T8721L-5mg 5mg Ask for price
Description: I-37 free base( 2359690-13-2(free base))

EDC free base

GM6988 5g
EUR 116.06

TMB free base

TB0954 1g
EUR 85.06

S107 free base

530577 100.0mg
EUR 750

NG25 free base

562503 5.0mg
EUR 485

R406 (free base)

A5880-100 100 mg
EUR 800
Description: Tyrosine Kinase|Spleen Tyrosine Kinase (Syk)

R406 (free base)

A5880-25 25 mg
EUR 320
Description: Tyrosine Kinase|Spleen Tyrosine Kinase (Syk)

R406 (free base)

A5880-5 5 mg
EUR 80
Description: Tyrosine Kinase|Spleen Tyrosine Kinase (Syk)

R406 (free base)

A5880-5.1 10 mM (in 1mL DMSO)
EUR 148
Description: Tyrosine Kinase|Spleen Tyrosine Kinase (Syk)

R406 (free base)

A5880-S Evaluation Sample
EUR 24
Description: Tyrosine Kinase|Spleen Tyrosine Kinase (Syk)

THZ1 (Free base)

9664-25 each
EUR 1227.6

THZ1 (Free base)

9664-5 each
EUR 352.8

K201 free base

414202 5.0mg
EUR 288

FIPI free base

407955 200.0mg
EUR 1050

FIPI (free base)

B2372-25 each
EUR 757.2

FIPI (free base)

B2372-5 each
EUR 235.2

R406(free base)

MBS131267-100mg 100mg
EUR 1065

R406(free base)

MBS131267-500mg 500mg
EUR 2775

SIS3 (free base)

HY-100444 10 mg
EUR 1244.61
Description: SIS3 free base is a potent and selective inhibitor of Smad3 phosphorylation. SIS3 free base inhibits the myofibroblast differentiation of fibroblasts by TGF-β1. SIS3 free base does not affect the phosphorylation of Smad2[1].

R406 (free base)

HY-11108 10mM/1mL
EUR 465.38
Description: R406 free base is an orally available and competitive Syk/FLT3 inhibitor for ATP binding with a Ki of 30 nM, potently inhibits Syk kinase activity in vitro with an IC50 of 41 nM, measured at an ATP concentration corresponding to its Km value. R406 free base reduces immune complex-mediated inflammation[1]. R406 free base also inhibits Lyn (IC50=63 nM) and Lck (IC50=37 nM)[2].

R406(free base)

E1KS1533 2mg
EUR 362.4

R406 free base

MBS3606124-10mg 10mg
EUR 305

R406 free base

MBS3606124-25mg 25mg
EUR 405

R406 free base

MBS3606124-2mg 2mg
EUR 235

R406 free base

MBS3606124-50mg 50mg
EUR 620

R406 free base

MBS3606124-5mg 5mg
EUR 260

R788 free base

MBS3606474-10mg 10mg
EUR 315

R788 free base

MBS3606474-25mg 25mg
EUR 430

R788 free base

MBS3606474-2mg 2mg
EUR 225

R788 free base

MBS3606474-5mg 5mg
EUR 260

R788 free base

MBS3606474-5x25mg 5x25mg
EUR 1620

SIS3 free base

MBS5767611-5mg 5mg
EUR 915

SIS3 free base

MBS5767611-5x5mg 5x5mg
EUR 3970

R406 (free base)

MBS8506526-2mg 2mg
EUR 440

R406 (free base)

MBS8506526-5x2mg 5x2mg
EUR 1835

R406 free base

T2467-10mg 10mg Ask for price
Description: R406 free base

R406 free base

T2467-1g 1g Ask for price
Description: R406 free base

R406 free base

T2467-1mg 1mg Ask for price
Description: R406 free base

R406 free base

T2467-50mg 50mg Ask for price
Description: R406 free base

R406 free base

T2467-5mg 5mg Ask for price
Description: R406 free base

SIS3 free base

T12923-10mg 10mg Ask for price
Description: SIS3 free base

SIS3 free base

T12923-1g 1g Ask for price
Description: SIS3 free base

SIS3 free base

T12923-1mg 1mg Ask for price
Description: SIS3 free base

SIS3 free base

T12923-50mg 50mg Ask for price
Description: SIS3 free base

SIS3 free base

T12923-5mg 5mg Ask for price
Description: SIS3 free base

ML355 free base

533249 50.0mg
EUR 350

ML241 free base

406621 10.0mg
EUR 90

MS023 free base

407274 10.0mg
EUR 150

LYS01 free base

407398 10.0mg
EUR 150

ML298 free base

407464 5.0mg
EUR 240

M2698 free base

407496 200.0mg
EUR 2950

AZ505 free base

407948 5.0mg
EUR 150

MA242 (free base)

HY-112816A Get quote Ask for price
Description: MA242 free base is a specific dual inhibitor of MDM2 and NFAT1. MA242 free base directly binds both MDM2 and NFAT1 with high affinity, induces their protein degradation, and inhibits NFAT1-mediated transcription of MDM2. MA242 free base induces apoptosis in pancreatic cancer cell lines regardless of p53 status[1].

YM158 (free base)

HY-U00355 1mg
EUR 2770.8

YM543 (free base)

HY-122613 Get quote Ask for price
Description: YM543 free base is a potent and orally active sodium-glucose cotransporter (SGLT) 2 inhibitor. YM543 free base reduces blood glucose levels. YM543 free base can be used in research of diabetes[1][2].

M1069 (free base)

HY-148088A Get quote Ask for price
Description: M1069 (free base) is a selective and orall active, dual A2A/A2B adenosine receptor antagonist with a selectivity of >100 fold against the A1 and A3 receptors. M1069 (free base) counteracts immune-suppressive mechanisms of adenosine, and exhibits anti-tumor activity[1][2][3].

AM095 free base

MBS3840238-10mg 10mg
EUR 230

AM095 free base

MBS3840238-25mg 25mg
EUR 370

AM095 free base

MBS3840238-5mg 5mg
EUR 190

AM095 free base

MBS3840238-5x25mg 5x25mg
EUR 1655

YM158 free base

MBS5766149-5mg 5mg
EUR 915

Sonidegib free base