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IDO-IN-1

CAT#: 406739
CAS#: 914638-30-5

IDO-IN-1 is a potent and selective indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50 of 59 nM. IDO-IN-1 showed...
10mg
Not available
25mg
Not available
50mg
USD 450
100mg
USD 750
200mg
USD 950
500mg
USD 1450
1g
USD 2450
2g
USD 3950
5g
Ask price
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Ravoxertinib

CAT#: 206065
CAS#: 1453848-26-4

Ravoxertinib also known as GDC-0994 and RG7842, is an orally available inhibitor of extracellular signal-regulated...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 650
200mg
USD 950
500mg
USD 1650
1g
USD 2850
2g
USD 4850
5g
Ask price
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LDN-193189

CAT#: 501105
CAS#: 1062368-24-4 (free base)

LDN193189 is a highly potent small molecule BMP inhibitor with IC50 of 5 and 30 nM for ALK2 and ALK3, respectively....
10mg
USD 90
25mg
USD 150
50mg
USD 250
100mg
USD 450
200mg
USD 750
500mg
USD 1450
1g
USD 2650
2g
USD 3850
5g
Ask price
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UNC-1999

CAT#: 406266
CAS#: 1431612-23-5

UNC1999, the first orally bioavailable inhibitor that has high in vitro potency for wildtype and mutant EZH2 as well...
10mg
USD 90
25mg
USD 150
50mg
USD 250
100mg
USD 450
200mg
USD 850
500mg
USD 1950
1g
USD 2950
2g
USD 4850
5g
USD 7650
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EPZ015666 (GSK3235025)

CAT#: 407226
CAS#: 1616391-65-1

EPZ015666, also known as GSK3235025, is a potent and selective and orally active PRMT5 inhibitor with a half-maximal...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 650
200mg
USD 1050
500mg
USD 2150
1g
USD 3250
2g
USD 4650
5g
USD 8450
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GSK591

CAT#: 407273
CAS#: 1616391-87-7

GSK591, also known as EPZ015866 and GSK3203591, is a chemical probe for PRMT5. In an in vitro biochemical assay,...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 750
200mg
USD 1250
500mg
USD 1950
1g
USD 3250
2g
USD 4350
5g
USD 7850
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CPI203

CAT#: 407122
CAS#: 1446144-04-2

CPI203, also known as TEN010, JQ-2; RO6870810 and RG6146, is a potent and orally active BET bromodomain inhibitor....
10mg
USD 190
25mg
USD 350
50mg
USD 550
100mg
USD 950
200mg
USD 1650
500mg
USD 2450
1g
USD 3250
2g
USD 3950
5g
USD 6950
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BMS-986205

CAT#: 206817
CAS#: 1923833-60-6 (free base)

Linrodostat, also known as BMS-986205, ONO-7701 and F001287, a potent and selective, orally active IDO1 inhibitor...
25mg
USD 150
50mg
USD 250
100mg
USD 450
200mg
USD 750
500mg
USD 1250
1g
USD 2150
2g
USD 3850
5g
USD 6950
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BAY-598 R-isomer

CAT#: 407403
CAS#: 1906920-28-2 (BAY598 R-isomer)

BAY-598 R-isomer is the R-isomer of BAY589. BAY-598 R-isomer may be used as a reference compound. BAY-598 is a...
5mg
USD 150
10mg
USD 250
25mg
USD 450
50mg
USD 750
100mg
USD 1250
200mg
USD 1950
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BAY-598

CAT#: 407278
CAS#: 1906919-67-2 (S-isomer)

BAY-598 is a potent, peptide-competitive chemical probe for SMYD2. BAY-598 has a unique chemotype relative to the...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 750
200mg
USD 1250
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Cilofexor

CAT#: 561844
CAS#: 1418274-28-8

Cilofexor, also known as GS-9674, is a farnesoid X receptor (FXR) agonist. The nonsteroidal FXR agonist cilofexor...
25mg
USD 365
50mg
USD 650
100mg
USD 1150
200mg
USD 2050
500mg
USD 2950
1g
USD 3950
2g
USD 6650
5g
USD 14950
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Tropifexor

CAT#: 329514
CAS#: 1383816-29-2

Tropifexor, also known as LJN452, is a farnesoid X receptor agonist for the Treatment of Cholestatic Liver Diseases...
5mg
USD 150
10mg
USD 250
25mg
USD 450
50mg
USD 750
100mg
USD 1250
200mg
USD 1850
500mg
USD 2950
1g
USD 3950
2g
USD 6950
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E7820

CAT#: 201090
CAS#: 289483-69-8

E7820 is a small molecule and aromatic sulfonamide derivative with potential antiangiogenic and antitumor activities....
50mg
USD 450
100mg
USD 750
200mg
USD 1250
500mg
USD 1950
1g
USD 2950
2g
USD 4650
5g
USD 7950
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SIS-17

CAT#: 555620
CAS#: 2374313-54-7

SIS17 is a potent and selective HDAC 11 inhibitor with an IC50 value of 0.83 μM. SIS17, is active in cells and...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 750
200mg
USD 1250
500mg
USD 1950
1g
USD 2950
2g
USD 4650
5g
USD 7650
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TD-139

CAT#: 528908
CAS#: 1450824-22-2

TD-139 is a galectin-3 inhibitor potentially for the treatment of idiopathic pulmonary fibrosis (IPF)
10mg
USD 450
25mg
USD 850
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Pexidartinib HCl

CAT#: 207104
CAS#: 2040295-03-0 (HCl)

Pexidartinib, also know as PLX-3397, is a CSF1R inhibitor with IC50 of 20 nM in development by Plexxikon for the...
100mg
USD 150
200mg
USD 250
500mg
USD 450
1g
USD 750
2g
USD 1250
5g
USD 2650
10g
USD 3850
20g
USD 6850
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Sardomozide HCl

CAT#: 200411
CAS#: 138794-73-7 (HCl salt)

Sardomozide HCl, also known as SAM486A or CGP48664, is a second-generation polyamine synthesis inhibitor, which...
5mg
USD 90
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 750
200mg
USD 1250
500mg
USD 2150
1g
USD 3650
2g
USD 5650
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RP-54745

CAT#: 555619
CAS#: 135330-08-4

RP-54745
1g
USD 3250
2g
USD 5450
5g
USD 7650
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XMD16-5

CAT#: 407372
CAS#: 1345098-78-3

XMD16-5 is a tyrosine kinase nonreceptor 2(TNK2) inhibitor. TNK2 mutations have been found in renal cancer cells and...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 850
200mg
USD 1450
500mg
USD 2150
1g
USD 3250
2g
USD 4950
5g
USD 7950
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XMD8-87

CAT#: 407375
CAS#: 1234480-46-6

XMD8-87 is a TNK2 inhibitor. XMD8-87 showed activity in the inhibition of TNK2 phosphorylation. XMD8-87 and XMD16-5...
10mg
USD 150
25mg
USD 250
50mg
USD 450
100mg
USD 750
200mg
USD 1250
500mg
USD 2150
1g
USD 3250
2g
USD 5450
5g
USD 9850
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MRTX1257

CAT#: 207086
CAS#: 2206736-04-9

MRTX1257 is a potent, selective, covalent and irreversible inhibitor of KRAS G12C, MRTX1257 inhibited KRAS dependent...
5mg
USD 150
10mg
USD 250
25mg
USD 450
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Rimeporide free base

CAT#: 330211
CAS#: 187870-78-6

Rimeporide, alaso known as EMD87580, is a potent, selective sodium hydrogen exchanger NHE1 inhibitor, show promise as...
1g
USD 3250
2g
USD 5650
5g
USD 7650
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DASA-58

CAT#: 555616
CAS#: 1203494-49-8

DASa-58, also known as ML-203 and NCGC00185916, is a selective activator of pyruvate kinase M2 (PKM2; AC50 = 38 nM in...
200mg
USD 1450
500mg
USD 2050
1g
USD 2950
2g
USD 5650
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SNJ-1945

CAT#: 564979
CAS#: 854402-59-8

SNJ-1945 is a calpain inhibitor with more favorable retinal penetration, high oral bioavailability, and long...
5mg
USD 190
10mg
USD 350
25mg
USD 650
50mg
USD 1050
100mg
USD 1750
200mg
USD 2950
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iCRT14

CAT#: 555248
CAS#: 677331-12-3

iCRT14 is a potent inhibitor of β-catenin-responsive transcription (CRT) that inhibits Wnt signaling in a reporter...
25mg
USD 150
50mg
USD 250
100mg
USD 450
200mg
USD 750
500mg
USD 1350
1g
USD 2450
2g
USD 4250