Vismodegib free base
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Vatalanib, Free Base |
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| 2026-5 | EUR 151.2 | |
Erlotinib, Free Base |
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| 2048-100 | EUR 189.6 | |
Erlotinib, Free Base |
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| 2048-1000 | EUR 464.4 | |
Sunitinib, Free base |
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| 2097-100 | EUR 229.2 | |
Sunitinib, Free base |
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| 2097-1000 | EUR 601.2 | |
Sunitinib, Free base |
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| 2097-25 | EUR 138 | |
Ruxolitinib (free base) |
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| 10-042 | 25 mg | EUR 418.2 |
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Description: Antineoplastic, anti-inflammatory and immunomodulating agent. Orally bioavailable potent ATP mimetic that inhibits both JAK1 and JAK2 with IC50 values of 2.7 and 4.5nM, respectively and is less selective for JAK3 (IC50=322nM). Affects DC differentiation and function, leading to impaired T cell activation. Used in the treatment of myeloproliferative neoplasms and psoriasis. Anticancer agent. Shown to induce apoptosis and autophagy. Potent and selective inhibitor of HIV-1 replication and virus reactivation in vitro. It is investigated against the spread of the SARS-CoV-2 (COVID-19). |
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Lapatinib, Free base |
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| 2138-100 | EUR 464.4 | |
Lapatinib, Free base |
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| 2138-25 | EUR 229.2 | |
Ruxolitinib, Free base |
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| 2139-100 | Ask for price | |
Ruxolitinib, Free base |
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| 2139-25 | EUR 639.6 | |
Ruxolitinib, Free base |
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| 2139-5 | EUR 248.4 | |
Imatinib, Free base |
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| 2141-100 | EUR 176.4 | |
Imatinib, Free base |
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| 2141-1000 | EUR 502.8 | |
Linsitinib, Free base |
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| 2294-25 | EUR 679.2 | |
Linsitinib, Free base |
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| 2294-5 | EUR 222 | |
Tipifarnib, Free base |
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| 2296-1 | EUR 170.4 | |
Tipifarnib, Free base |
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| 2296-5 | EUR 496.8 | |
Rucaparib (free base) |
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| A8893-10 | 10 mg | EUR 240 |
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Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. |
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Rucaparib (free base) |
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| A8893-200 | 200 mg | EUR 1243.2 |
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Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. |
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Rucaparib (free base) |
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| A8893-5 | 5 mg | EUR 164.4 |
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Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. |
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Rucaparib (free base) |
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| A8893-5.1 | 10 mM (in 1mL DMSO) | EUR 170.4 |
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Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. |
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Rucaparib (free base) |
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| A8893-50 | 50 mg | EUR 547.2 |
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Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. |
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LY2835219 free base |
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| A3575-100 | 100 mg | EUR 686.4 |
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Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity. |
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LY2835219 free base |
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| A3575-25 | 25 mg | EUR 309.6 |
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Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity. |
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LY2835219 free base |
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| A3575-5 | 5 mg | EUR 170.4 |
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Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity. |
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R406 (free base) |
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| A5880-100 | 100 mg | EUR 1452 |
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Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins. |
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R406 (free base) |
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| A5880-25 | 25 mg | EUR 616.8 |
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Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins. |
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R406 (free base) |
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| A5880-5 | 5 mg | EUR 199.2 |
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Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins. |
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R406 (free base) |
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| A5880-5.1 | 10 mM (in 1mL DMSO) | EUR 316.8 |
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Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins. |
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R406 (free base) |
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| A5880-S | Evaluation Sample | EUR 97.2 |
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Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins. |
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THZ1 (Free base) |
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| 9664-25 | EUR 1227.6 | |
THZ1 (Free base) |
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| 9664-5 | EUR 352.8 | |
MCC950 (Free base) |
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| B1031-1 | EUR 183.6 | |
MCC950 (Free base) |
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| B1031-5 | EUR 548.4 | |
FIPI (free base) |
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| B2372-25 | EUR 757.2 | |
FIPI (free base) |
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| B2372-5 | EUR 235.2 | |
Terbinafine (Free base) |
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| B2423-250 | EUR 248.4 | |
Terbinafine (Free base) |
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| B2423-50 | EUR 144 | |
PLX5622 (free base) |
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| B2965-25 | 25 mg | EUR 903.6 |
PLX5622 (free base) |
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| B2965-5 | 5 mg | EUR 272.4 |
Apatinib (Free base) |
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| B1613-25 | EUR 496.8 | |
Apatinib (Free base) |
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| B1613-5 | EUR 170.4 | |
Carubicin (Free base) |
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| B1853-1 | EUR 183.6 | |
Carubicin (Free base) |
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| B1853-5 | EUR 548.4 | |
AZD4547, Free Base |
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| ADC-P-063 | unit | Ask for price |
AZD8055, Free Base |
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| ADC-P-064 | unit | Ask for price |
Cyclopamine, Free Base |
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| ADC-P-079 | unit | Ask for price |
Ixabepilone, Free Base |
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| ADC-P-104 | unit | Ask for price |
R406(free base) |
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| E1KS1533 | 2mg | EUR 625.2 |
Ripasudil free base |
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| HY-15685A | 10mg | EUR 489.6 |
Vatalanib (free base) |
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| HY-10203 | 5mg | EUR 142.8 |
RPR107393 free base |
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| HY-100299 | 1mg | EUR 577.2 |
FR167344 free base |
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| HY-100301 | 1mg | EUR 3164.4 |
FR183998 free base |
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| HY-100302 | 1mg | EUR 1352.4 |
FR194738 free base |
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| HY-100303 | 1mg | EUR 2388 |
YM158 (free base) |
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| HY-U00355 | 1mg | EUR 2770.8 |
Masupirdine (free base) |
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| HY-109118 | 1mg | EUR 267.6 |
R406 (free base) |
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| HY-11108 | 10mM/1mL | EUR 277.2 |
ITI214 (free base) |
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| HY-12501 | 100mg | EUR 3531.6 |
AS2863619 (free base) |
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| HY-126675 | 5mg | EUR 1410 |
AZD3839 (free base) |
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| HY-13438 | 50mg | EUR 1216.8 |
TMB free base |
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| TB0954 | 1g | EUR 85.06 |
Xylazine (free base) |
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| Q-1445.0025 | 25.0g | EUR 385.2 |
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Description: Sum Formula: C12H16N2S; CAS# [7361-61-7] |
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Vismodegib |
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| 20-abx076843 |
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Vismodegib |
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| 20-abx182703 |
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Vismodegib |
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| HY-10440 | 10mM/1mL | EUR 151.2 |
RGB-286638, free base |
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| 2886-25 | EUR 907.2 | |
RGB-286638, free base |
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| 2886-5 | EUR 274.8 | |
GSK-J4 (Free base) |
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| 2762-1 | EUR 144 | |
GSK-J4 (Free base) |
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| 2762-5 | EUR 314.4 | |
StemRegenin 1, Free base |
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| 2642-1 | EUR 157.2 | |
StemRegenin 1, Free base |
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| 2642-5 | EUR 398.4 | |
AM-095 free base |
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| A3167-10 | 10 mg | EUR 254.4 |
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Description: AM095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (LPA1) with IC50 values of 0.73 and 0.98 ?M for mouse or recombinant human LPA1, respectively [1]. |
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AM-095 free base |
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| A3167-100 | 100 mg | EUR 964.8 |
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Description: AM095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (LPA1) with IC50 values of 0.73 and 0.98 ?M for mouse or recombinant human LPA1, respectively [1]. |
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AM-095 free base |
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| A3167-200 | 200 mg | EUR 1382.4 |
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Description: AM095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (LPA1) with IC50 values of 0.73 and 0.98 ?M for mouse or recombinant human LPA1, respectively [1]. |
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AM-095 free base |
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| A3167-5 | 5 mg | EUR 199.2 |
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Description: AM095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (LPA1) with IC50 values of 0.73 and 0.98 ?M for mouse or recombinant human LPA1, respectively [1]. |
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AM-095 free base |
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| A3167-50 | 50 mg | EUR 686.4 |
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Description: AM095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (LPA1) with IC50 values of 0.73 and 0.98 ?M for mouse or recombinant human LPA1, respectively [1]. |
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SGI-1776 free base |
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| A4192-10 | 10 mg | EUR 296.4 |
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Description: SGI-1776 free base, N-((1-methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, is a potent ATP-competitive inhibitor of the serine/threonine family of Pim kinase, an enzyme regulating cell survival. |
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SGI-1776 free base |
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| A4192-5 | 5 mg | EUR 184.8 |
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Description: SGI-1776 free base, N-((1-methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, is a potent ATP-competitive inhibitor of the serine/threonine family of Pim kinase, an enzyme regulating cell survival. |
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SGI-1776 free base |
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| A4192-5.1 | 10 mM (in 1mL DMSO) | EUR 199.2 |
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Description: SGI-1776 free base, N-((1-methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, is a potent ATP-competitive inhibitor of the serine/threonine family of Pim kinase, an enzyme regulating cell survival. |
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SGI-1776 free base |
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| A4192-50 | 50 mg | EUR 630 |
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Description: SGI-1776 free base, N-((1-methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, is a potent ATP-competitive inhibitor of the serine/threonine family of Pim kinase, an enzyme regulating cell survival. |
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SGI-1776 free base |
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| A4192-S | Evaluation Sample | EUR 97.2 |
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Description: SGI-1776 free base, N-((1-methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, is a potent ATP-competitive inhibitor of the serine/threonine family of Pim kinase, an enzyme regulating cell survival. |
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L-Arginine free base |
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| AB0205 | 100g | EUR 75.78 |
GSK J4 free base |
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| B5959-10 | 10 mg | EUR 447.6 |
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Description: GSK J4 free base |
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GSK J4 free base |
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| B5959-50 | 50 mg | EUR 1437.6 |
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Description: GSK J4 free base |
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