Newest Products

AFN-1252

CAT#: 526918
CAS#: 620175-39-5

AFN-1252, also known as AFN-12520000; API-1252; Debio-1452, is an enoyl-(acyl-carrier protein) reductase fabl...

Vatiquinone

CAT#: 319685
CAS#: 1213269-98-7

Vatiquinone, also known as EPI 743, is an orally bioavailable para-benzoquinone being developed for inherited...

RBN012759

CAT#: 207164
CAS#: 2360851-29-0

RBN012759 is a potent and selective PARP14 inhibitor which decreases protumor macrophage gene expression and elicits...

Adavivint

CAT#: 573428
CAS#: 1467093-03-3 (free base)

Adavivint, also known as SM04690, is a small-molecule inhibitor of the Wnt pathway which is being investigated as a...

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...

ML109

CAT#: 555782
CAS#: 1186649-91-1

ML-109, also known as CID-25246343, is a potent and full thyroid stimulating hormone receptor (TSHR) agonist. ML109...

ALC-0315

CAT#: 556006
CAS#: 2036272-55-4

ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily material, It has attracted...

Merafloxacin

CAT#: 333957
CAS#: 91188-00-0

Merafloxacin, also known as CI 934, is a fluoroquinolone antibacterial, which was also identified as a −1 PRF...

RU320521

CAT#: 555738
CAS#: 2262452-06-0

RU320521, also known as RU521; RU.521 is a potent and selective inhibitor of cGAS, inhibiting cGAS-mediated...

MUN36378

CAT#: 556026
CAS#: 2243736-37-8

MUN36378 is a FTO inhibitor for treatment of leukemia. This compound was first reported in patent WO 2018157842. This...

PS210

CAT#: 562629
CAS#: 1221962-86-2

PS210 is a substrate-selective inhibitor of protein kinase PDK1. It acts by binding to the PIF-pocket allosteric...

CUN79177

CAT#: 556025
CAS#: 2270879-17-7

CUN79177, also known as BRM/BRG1 ATP Inhibitor-1, is an orally Active Inhibitors (IC50=5 nM) of Brahma Homolog...

E3L-4133

CAT#: 555511
CAS#: 1264754-13-3

E3L-4133, also known as E3 ligase Ligand 5, is an E3 ligase Ligand that can be used in PROTAC (proteolysis targeting...

Ribociclib HCl

CAT#: 206739
CAS#: 1211443-80-9 (HCl)

Ribociclib hydrochloride is an potent and orally available cyclin-dependent kinase (CDK) inhibitor targeting cyclin...

ERD-308

CAT#: 407957
CAS#: 2320561-35-9

ERD-308 is a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Estrogen Receptor (ER) ERD-308 achieves...

Darinaparsin

CAT#: 200850
CAS#: 69819-86-9

Darinaparsin, also know as ZIO-101 and SP-02, is a small-molecule organic arsenical with potential antineoplastic...

Vardenafil hydrochloride trihydrate

CAT#: 326826
CAS#: 330808-88-3

Vardenafil, also known as BAY 38-9456, is a PDE5 inhibitor used for treating erectile dysfunction. Vardenafil (VAR)...

DUN41875

CAT#: 556024
CAS#: 1295541-87-5

DUN41875, also known as SCD1 inhibitor-4, is a potent, orally active stearoylCoA desaturase-1 (SCD1) inhibitor. SCD1...

GSK620

CAT#: 555971
CAS#: 2088410-46-0

GSK620 is a Potent, selective, and Highly Soluble Bromo and Extraterminal Domain (BET) Second Bromodomain (BD2)...

Maropitant free base

CAT#: 120201
CAS#: 147116-67-4 (free base)

Maropitan, also known as CJ 11972, is a neurokinin (NK1) receptor antagonist, which was developed by Zoetis...

XL092

CAT#: 555990
CAS#: 2367004-54-2

XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and MER, with IC50 values in...

Sildenafil Citrate

CAT#: 318693
CAS#: 171599-83-0 (citrate)

Sildenafil is a selective inhibitor of PDE5 (type 5 cGMP phosphodiesterase) which catalyzes the hydrolysis of...

Oxytocin acetate

CAT#: 319932
CAS#: 6233-83-6 (acetate)

Oxytocin is a medication and hormone. As a medication, it is used to cause contraction of the uterus, which is used...

BDP9066

CAT#: 563970
CAS#: 2226507-04-4

BDP9066 is a potent and selective MRCK inhibitor with an IC50 of 64 nM for MRCKβ in SCC12 cells, Ki values of 0.0136...

CC90001 free base

CAT#: 555913
CAS#: 1403859-14-2 (free base)

CC-90001 is a potent and selective JNK inhibitor, which is 12.9-fold more potent for JNK1 inhibition than JNK2 in a...