Bortezomib, free base, 100mg

Bortezomib, free base, 100mg 

To Order Contact us: lieven@wlsolutions.be

Bortezomib

GP0262-25 25
EUR 216.3

Bortezomib

GP0262-5 5
EUR 98.4

Bortezomib, 99%

BC010-005 5mg Ask for price

Bortezomib, 99%

BC010-010 10mg
EUR 213.6

Bortezomib, 99%

BC010-025 25mg
EUR 264

Bortezomib, 99%

BC010-050 50mg
EUR 327.6

Bortezomib, 99%

BC010-500 500mg
EUR 724.8

Bortezomib (PS-341)

A2614-10 10 mg
EUR 142.8
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (PS-341)

A2614-100 100 mg
EUR 408
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (PS-341)

A2614-25 25 mg
EUR 208.8
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (PS-341)

A2614-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (PS-341)

A2614-500 500 mg
EUR 1005.6
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (PS-341)

A2614-S Evaluation Sample
EUR 97.2
Description: Bortezomib (originally codenamed PS-341) is the first therapeutic proteasome inhibitor to the tested in humans. It is approved in the U.S. for treating relapsed multiple myeloma and mantle cell lymphoma.

Bortezomib (BTZ) Protein (BSA)

20-abx651876
  • EUR 693.60
  • EUR 309.60
  • EUR 2064.00
  • EUR 828.00
  • EUR 510.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

Bortezomib (BTZ) Protein (OVA)

20-abx651877
  • EUR 693.60
  • EUR 309.60
  • EUR 2064.00
  • EUR 828.00
  • EUR 510.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

BSA Conjugated Bortezomib (BTZ)

4-CPK684Ge11
  • EUR 496.32
  • EUR 256.80
  • EUR 1531.20
  • EUR 590.40
  • EUR 1060.80
  • EUR 408.00
  • EUR 3648.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
Description: Recombinant Pan-species Bortezomib expressed in: E.coli

OVA Conjugated Bortezomib (BTZ)

4-CPK684Ge21
  • EUR 496.32
  • EUR 256.80
  • EUR 1531.20
  • EUR 590.40
  • EUR 1060.80
  • EUR 408.00
  • EUR 3648.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
Description: Recombinant Pan-species Bortezomib expressed in: E.coli

Bortezomib (Proteasome inhibitor)

SIH-328-25MG 25 mg
EUR 192
Description: The substance Bortezomib is a proteasome inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white powder which is soluble in 50 mg/ml DMSO, 35 mg/ml Ethanol.

Bortezomib (Proteasome inhibitor)

SIH-328-5MG 5 mg
EUR 138
Description: The substance Bortezomib is a proteasome inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white powder which is soluble in 50 mg/ml DMSO, 35 mg/ml Ethanol.

Biotin-X, free acid:100mg

90053 100MG
EUR 158.4
Description: Minimum order quantity: 1 unit of 100MG

Bioin-XX, free acid: (100mg)

90054 100MG
EUR 258
Description: Minimum order quantity: 1 unit of 100MG

TMB free base

TB0954 1g
EUR 85.06

FIPI (free base)

B2372-25 each
EUR 757.2

FIPI (free base)

B2372-5 each
EUR 235.2

THZ1 (Free base)

9664-25 each
EUR 1227.6

THZ1 (Free base)

9664-5 each
EUR 352.8

R406 (free base)

A5880-100 100 mg
EUR 1452
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.

R406 (free base)

A5880-25 25 mg
EUR 616.8
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.

R406 (free base)

A5880-5 5 mg
EUR 199.2
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.

R406 (free base)

A5880-5.1 10 mM (in 1mL DMSO)
EUR 316.8
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.

R406 (free base)

A5880-S Evaluation Sample
EUR 97.2
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.

R406(free base)

E1KS1533 2mg
EUR 625.2

R406 (free base)

HY-11108 10mM/1mL
EUR 277.2

YM158 (free base)

HY-U00355 1mg
EUR 2770.8

MCC950 (Free base)

B1031-1 each
EUR 183.6

MCC950 (Free base)

B1031-5 each
EUR 548.4

ITI214 (free base)

HY-12501 100mg
EUR 3531.6

PLX5622 (free base)

B2965-25 25 mg
EUR 903.6

PLX5622 (free base)

B2965-5 5 mg
EUR 272.4

AZD4547, Free Base

ADC-P-063 unit Ask for price

AZD8055, Free Base

ADC-P-064 unit Ask for price

AZD3839 (free base)

HY-13438 50mg
EUR 1216.8

Apatinib (Free base)

B1613-25 each
EUR 496.8

Apatinib (Free base)

B1613-5 each
EUR 170.4

Imatinib, Free base

2141-100 each
EUR 176.4

Imatinib, Free base

2141-1000 each
EUR 502.8

FR167344 free base

HY-100301 1mg
EUR 3164.4

FR183998 free base

HY-100302 1mg
EUR 1352.4

FR194738 free base

HY-100303 1mg
EUR 2388

Xylazine (free base)

Q-1445.0025 25.0g
EUR 385.2
Description: Sum Formula: C12H16N2S; CAS# [7361-61-7]

Lapatinib, Free base

2138-100 each
EUR 464.4

Lapatinib, Free base

2138-25 each
EUR 229.2

Erlotinib, Free Base

2048-100 each
EUR 189.6

Erlotinib, Free Base

2048-1000 each
EUR 464.4

Sunitinib, Free base

2097-100 each
EUR 229.2

Sunitinib, Free base

2097-1000 each
EUR 601.2

Sunitinib, Free base

2097-25 each
EUR 138

Vatalanib, Free Base

2026-25 each
EUR 366

Vatalanib, Free Base

2026-5 each
EUR 151.2

LY2835219 free base

A3575-100 100 mg
EUR 686.4
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.

LY2835219 free base

A3575-25 25 mg
EUR 309.6
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.

LY2835219 free base

A3575-5 5 mg
EUR 170.4
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.

Carubicin (Free base)

B1853-1 each
EUR 183.6

Carubicin (Free base)

B1853-5 each
EUR 548.4

Rucaparib (free base)

A8893-10 10 mg
EUR 240
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.

Rucaparib (free base)

A8893-200 200 mg
EUR 1243.2
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.

Rucaparib (free base)

A8893-5 5 mg
EUR 164.4
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.

Rucaparib (free base)

A8893-5.1 10 mM (in 1mL DMSO)
EUR 170.4
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.

Rucaparib (free base)

A8893-50 50 mg
EUR 547.2
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.

RPR107393 free base

HY-100299 1mg
EUR 577.2

Vatalanib (free base)

HY-10203 5mg
EUR 142.8

Ripasudil free base

HY-15685A 10mg
EUR 489.6

AS2863619 (free base)

HY-126675 5mg
EUR 1410

Linsitinib, Free base

2294-25 each
EUR 679.2

Linsitinib, Free base

2294-5 each
EUR 222

Tipifarnib, Free base

2296-1 each
EUR 170.4

Tipifarnib, Free base

2296-5 each
EUR 496.8

Nintedanib (free base)

GW5215-100 100
EUR 274.7

Nintedanib (free base)

GW5215-25 25
EUR 117.8

Terbinafine (Free base)

B2423-250 each
EUR 248.4

Terbinafine (Free base)

B2423-50 each
EUR 144

Ruxolitinib (free base)

10-042 25 mg
EUR 418.2
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).

Bortezomib, free base, 100mg