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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
25139Olomorasibum2771246-13-898% Min.
Olomorasibumis a Kirsten rat sarcoma viral oncogene homolog (KRAS) inhibitor, antineo
25116Orelabrutinib1655504-04-398% Min.
Orelabrutinib, also known as ICP-022, is a potent, orally active, and irreversible Br
25083Orteronel566939-85-398% Min.
Orterone, also known as TAK-700, is an orally bioavailable non-steroidal androgen syn
25060OPN expression inhibitor 12257492-95-698% Min.
OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
25040Opiranserin HCl1440796-75-7 (HCl)98% Min.
Opiranserin HCl is a glycine transporter inhibitor and serotonin receptor antagonist.
24091Ocedurenone1359969-24-698% Min.
Ocedurenone is a non-steroidal mineralocorticoid receptor antagonist.
24047Opevesostat2231294-96-398% Min.
Opevesostat is cholesterol side-chain cleavage enzyme (CYP11A1) inhibitor.
24046Olverembatinib (GZD824)1257628-77-598% Min.
Olverembatinib, also known as GZD824, is a novel orally bioavailable inhibitor agains
20642OATD-022146132-73-0≧98.0%
OATD-02, an orally available dual arginase inhibitor (ARG1 and ARG2), is in phase I c
20625Orismilast ( LEO-32731 )1353546-86-7≧98.0%
Orismilast is a phosphodiesterase type 4 (PDE4) inhibitor.
20600Odevixibat501692-44-098% Min.
Odevixibat, also known as AZD 8294, is a potent, once-daily, non-systemic ileal bile
20571O4I4412008-21-098% Min.
O4I4 (compound 23) is a OCT4-inducing compound with metabolical stability.
20537orforglipron2212020-52-398% Min.
Orforglipron, also known as LY3502970, and OWL-833, is a Novel Non-Peptidyl Oral Gluc
20530omaveloxolone1474034-05-398% Min.
Omaveloxolone, also known as RTA-408, is a member of the synthetic oleanane triterpen
20505Osanetant160492-56-8 (free base)98% Min.
Osanetant is a tachykinin NK3 antagonist potentially for the treatment of schizophren
20314Obicetrapib866399-87-398% Min.
Obicetrapib (also known as AMG-899, TA-8995, and DEX-001) is a cholesteryl ester tran
20305ONC201 HCl1638178-82-198% Min.
ONC-201, also known as TIC10 and imipridone, is a potent, orally active, and stable s
2091912OUN209852244520-98-598% Min.
OUN20985, also known as Homo-PROTAC cereblon degrader 1, is a cereblon degrader. OUN2
208191OATD-01 (GLPG-4716)2088453-21-6≧98.0%
OATD-01 (GLPG-4716), a dual inhibitor of acidic mammalian chitinase (AMCase) and chit
2071536Oroxylin A480-11-598% Min.
Oroxylin A is a flavonoid that inhibits decreases in cell viability and increases in
2071504O3041261289-04-698% Min.
O-304 is a pan-activator of AMP-activated protein kinase (AMPK). It increases levels
20791Olutasidenib1887014-12-198%
Olutasidenib (FT-2102) is a potent mutant-selective IDH1 inhibitor. Olutasidenib (FT-
2051503OUN87710502887-71-098% Min.
OUN87710, also known as MMP-9-IN-1 is a specific matrix metalloproteinase-9 (MMP-9) i
2041232-oxo-5,5-diphenyltetrahydro-4-furancarboxylic acid79371-39-4≧96.0%
111895Oteseconazole1340593-59-0≧98.0%
Oteseconazole, also known as VT-1161,is the first Approved Orally Bioavailable and Se
111891ONC2061638178-87-698% Min.
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th
193186Ogerin 1309198-71-7>98%
Ogerin is a selective GPR68 PAM, suppressing recall in fear conditioning in wild-type
1810162ONO-85905801802661-73-9>98%
ONO-8590580 is a GABAA α5 negative allosteric modulator.
186291Ombrabulin HCl253426-24-3>98%
Ombrabulin is a synthetic water-soluble analogue of combretastatin A4, derived from t
186154Oligomycin A579-13-5>98%
Oligomycin A, also known as MCH 32, is an inhibitor of ATP synthase.