| R10797 |
CWHM-12 |
CWHM-12 a novel small molecule inhibitor of αV integrins with IC50s of 1.8/0.8/1
|
| R10799 |
LCL161 Enantiomer |
LCL161 is an orally bioavailable second mitochondrial-derived activator of caspa
|
| R10801 |
Deltarasin |
Deltarasin is a small molecular inhibitor of KRAS-PDEδ interaction with Kd of 38
|
| R10802 |
Nutlin-3 |
MDM2 antagonist nutlin-3 is a potent inducer of apoptosis.
|
| R10803 |
PX478 dihydrochloride |
PX-478 2HCl is an orally active, and selective hypoxia-inducible factor-1α (HIF-
|
| R10804 |
INNO-206; Aldoxorubicin HCl |
|
| R10805 |
Elacridar HCl |
Elacridar hydrochloride is a P-glycoprotein inhibitor, and has been used both in
|
| R10808 |
PTZ-343; phenothiazine sodium salt |
PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi
|
| R10809 |
Golotimod; SCV 07 |
Golotimod is an orally bioavailable synthetic peptide containing the amino acids
|
| R10810 |
Uramustine |
Uramustine is a chemotherapy drug which belongs to the class of alkylating agent
|
| R10813 |
ARRY-520 |
KSP inhibitor ARRY-520 specifically inhibits KSP (kinesin-5 or Eg5) with potenti
|
| R10814 |
Muscimol HBr |
Muscimol hydrobromide is a potent but toxic structural analog of g-aminobutyric
|
| R10815 |
Oprozomib (ONX 0912; PR047) |
Oprozomib (ONX 0912) is an orally bioavailable inhibitor for CT-L activity of 20
|
| R10816 |
Tretazicar (CB 1954) |
Tretazicar (CB 1954), an antitumor prodrug, is highly selective against the Walk
|
| R10817 |
Pelitrexol |
Pelitrexol (AG 2037) is an inhibitor of glycinamide ribonucleotide formyltransfe
|
| R10818 |
Varlitinib; ARRY 543 |
Varlitinib is a selective and potent ErbB1(EGFR) and ErbB2(HER2) inhibitor with
|
| R10820 |
RO08-2750 |
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) i
|
| R10821 |
(1R,2R)-2-fluorocyclopropanecarboxylic acid |
|
| R10822 |
PTZ-343 |
PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi
|
| R10823 |
BOC-4-HYDROXY-L-PYRROLIDINE LACTONE |
|
| R10825 |
Gemcitabine elaidate(CP-4126; CO-101) |
Gemcitabine elaidate(CP-4126; CO-101) is a lipophilic, unsaturated fatty acid es
|
| R10827 |
RG7112 (Synonyms: RO5045337) |
RG7112 is the first clinical small-molecule MDM2 inhibitor designed to occupy th
|
| R10828 |
HO-3867 |
HO-3867, an analog of curcumin, is a selective STAT3 inhibitor.
|
| R10829 |
SCH772984 |
SCH772984 is a novel, specific inhibitor of ERK1/2 with IC50 of 4 nM and 1 nM in
|
| R10830 |
Tenofovir disoproxil fumarate |
Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inh
|