Vismodegib free base
To Order Contact us: lieven@wlsolutions.be
Masupirdine (free base) |
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| HY-109118 | 1mg | EUR 223 |
R406 (free base) |
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| HY-11108 | 10mM/1mL | EUR 231 |
ITI214 (free base) |
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| HY-12501 | 100mg | EUR 2943 |
AS2863619 (free base) |
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| HY-126675 | 5mg | EUR 1175 |
AZD3839 (free base) |
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| HY-13438 | 50mg | EUR 1014 |
RPR107393 free base |
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| HY-100299 | 1mg | EUR 481 |
FR167344 free base |
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| HY-100301 | 1mg | EUR 2637 |
FR183998 free base |
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| HY-100302 | 1mg | EUR 1127 |
FR194738 free base |
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| HY-100303 | 1mg | EUR 1990 |
Vatalanib (free base) |
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| HY-10203 | 5mg | EUR 119 |
YM158 (free base) |
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| HY-U00355 | 1mg | EUR 2309 |
R406(free base) |
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| E1KS1533 | 2mg | EUR 521 |
TMB free base |
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| TB0954 | 1g | EUR 70.88 |
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 |
Xylazine (free base) |
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| Q-1445.0025 | 25.0g | EUR 321 |
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Description: Sum Formula: C12H16N2S; CAS# [7361-61-7] |
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R406 (free base) |
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| A5880-100 | 100 mg | EUR 1210 |
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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 514 |
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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 166 |
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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 264 |
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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 81 |
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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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Rucaparib (free base) |
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| A8893-10 | 10 mg | EUR 200 |
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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 1036 |
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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 137 |
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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 142 |
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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 456 |
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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 572 |
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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 258 |
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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 142 |
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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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Ruxolitinib (free base) |
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| 10-042 | 25 mg | EUR 348.5 |
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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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MCC950 (Free base) |
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| B1031-1 | EUR 153 | |
MCC950 (Free base) |
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| B1031-5 | EUR 457 | |
Apatinib (Free base) |
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| B1613-25 | EUR 414 | |
Apatinib (Free base) |
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| B1613-5 | EUR 142 | |
Carubicin (Free base) |
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| B1853-1 | EUR 153 | |
Carubicin (Free base) |
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| B1853-5 | EUR 457 | |
Anlotinib, free base |
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| B2156-25 | EUR 588 | |
Anlotinib, free base |
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| B2156-5 | EUR 185 | |
FIPI (free base) |
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| B2372-25 | EUR 631 | |
FIPI (free base) |
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| B2372-5 | EUR 196 | |
Terbinafine (Free base) |
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| B2423-250 | EUR 207 | |
Terbinafine (Free base) |
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| B2423-50 | EUR 120 | |
PLX5622 (free base) |
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| B2965-25 | 25 mg | EUR 753 |
PLX5622 (free base) |
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| B2965-5 | 5 mg | EUR 227 |
THZ1 (Free base) |
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| 9664-25 | EUR 1023 | |
THZ1 (Free base) |
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| 9664-5 | EUR 294 | |
Vatalanib, Free Base |
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| 2026-25 | EUR 305 | |
Vatalanib, Free Base |
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| 2026-5 | EUR 126 | |
Erlotinib, Free Base |
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| 2048-100 | EUR 158 | |
Erlotinib, Free Base |
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| 2048-1000 | EUR 387 | |
Sunitinib, Free base |
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| 2097-100 | EUR 191 | |
Sunitinib, Free base |
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| 2097-1000 | EUR 501 | |
Sunitinib, Free base |
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| 2097-25 | EUR 115 | |
Lapatinib, Free base |
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| 2138-100 | EUR 387 | |
Lapatinib, Free base |
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| 2138-25 | EUR 191 | |
Ruxolitinib, Free base |
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| 2139-100 | Ask for price | |
Ruxolitinib, Free base |
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| 2139-25 | EUR 533 | |
Ruxolitinib, Free base |
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| 2139-5 | EUR 207 | |
Imatinib, Free base |
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| 2141-100 | EUR 147 | |
Imatinib, Free base |
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| 2141-1000 | EUR 419 | |
Linsitinib, Free base |
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| 2294-25 | EUR 566 | |
Linsitinib, Free base |
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| 2294-5 | EUR 185 | |
Tipifarnib, Free base |
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| 2296-1 | EUR 142 | |
Tipifarnib, Free base |
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| 2296-5 | EUR 414 | |
Vismodegib |
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| HY-10440 | 10mM/1mL | EUR 126 |
Vismodegib |
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| 20-abx076843 |
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Vismodegib |
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| 20-abx182703 |
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JTV-519 (free base) |
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| HY-15293A | 5mg | EUR 567 |
RGB-286638 (free base) |
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| HY-15504A | 100mg | EUR 2804 |
DOV-216,303 (Free Base) |
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| HY-18332C | 10mM/1mL | EUR 492 |
SB-334867 (free base) |
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| HY-10895A | 10mg | EUR 215 |
SNT-207858 (free base) |
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| HY-11030A | 10mg | EUR 911 |
APX-115 (free base) |
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| HY-120801A | 5mg | EUR 223 |
LY-2584702 (free base) |
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| HY-12493 | 5mg | EUR 165 |
Genz-123346 (free base) |
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| HY-12744 | 10mM/1mL | EUR 189 |
YHO-13351 (free base) |
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| HY-12758A | 10mM/1mL | EUR 176 |
FK-448 Free base |
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| HY-100193 | 10mg | EUR 1887 |
KW-8232 free base |
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| HY-100304 | 10mg | EUR 5018 |
YM-53601 free base |
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| HY-100313 | 1mg | EUR 1559 |
AV-412 (free base) |
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| HY-10346A | 5mg | EUR 173 |
CP-319340(free base) |
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| HY-U00270 | 5mg | EUR 877 |
Staurosporine, >99% Free Base |
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| BC090-001 | 1mg | EUR 246 |
Staurosporine, >99% Free Base |
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| BC090-005 | 5mg | EUR 340 |
Vandetanib, >99% Free Base |
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| BC098-025 | 25mg | EUR 232 |