Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
21228 | SNG-1153 | 1446712-19-1 | 98% Min. | |
SNG-1153 is a modulator of estrogen receptor ER-alpha36. | ||||
81498 | Seltorexant | 1293281-49-8 | 98% Min. | |
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor | ||||
20123103 | (S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)- 1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol | 2301974-60-5 | 98% Min. | |
20103002 | Senaparib | 1401682-78-7 | ≧98.0% | |
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with | ||||
2091901 | SAR 131675 | 1433953-83-3 | 98% Min. | |
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine | ||||
2091205 | (1S,5R)-1-(3-fluorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one | 528587-70-4 | 98% Min. | |
2071609 | SJB2-043 | 63388-44-3 | 98% Min. | |
SJB2-043 is an inhibitor of USP1 target ID1 degradation in leukemic cells. | ||||
2071521 | Spastazoline | 2351882-11-4 | 98% Min. | |
Spastazoline is a novel inhibitor for aaa+ (atpases associated with diverse cellular | ||||
2071510 | SB 225002 | 18298-32-4 | 98% Min. | |
2071501 | SCH-23390 maleate | 87134-87-0 | 98% Min. | |
SCH-23390 hydrochloride is a potent dopamine receptor antagonist (Ki values are 0.2 n | ||||
202331 | ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol | 1369767-20-3 | ≧96.0% | |
The bulk may be provided by custom synthesis. | ||||
2062002 | (S)-4-(((1-Propyl-1H-imidazol-5-yl)methyl)sulfinyl)aniline | 497223-38-8 | 96% Min. | |
2051514 | SJ000291942 | 425613-09-8 | 98% Min. | |
SJ000291942 is a bone morphogenic protein (BMP) signaling activator. | ||||
2051502 | Selinexor HCl | Unknown (HCl) | 98% Min. | |
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO | ||||
2051501 | Selinexor free base | 1393477-72-9 (free base) | 98% Min. | |
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO | ||||
2041504 | Simurosertib | 1330782-76-7 | 98% Min. | |
Simurosertib, also known as TAK-931, is an orally bioavailable inhibitor of cell divi | ||||
204609 | SGC2085 free base | 1821908-48-8 (free base) | 98% Min. | |
SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1 | ||||
204501 | Segetalin B | 164991-89-3 | 98% Min. | |
Segetalin B is natural product isolated from Seeds of Vaccaria Segetalis. Segetalin B | ||||
112592 | S26131 | 296280-56-3 | 98% Min. | |
S26131 is a bioactive chemical. | ||||
111896 | SI113 | 1392816-46-4 | 98% Min. | |
SI113 is a specific inhibitor of the Sgk1 kinase activity, counteracting cancer cell | ||||
196301 | 3-[(1S)-1-aminoethyl]-8-chloro-2-phenyl-1,2-dihydroisoquinolin-1-one | 1350643-72-9 | 96% Min. | |
52001 | Selisistat ( EX-527 ) | 49843-98-3 | ≧98.0% | |
Selisistatwas the first identified potent and cell permeable SIRT1-specific inhibitor | ||||
193261 | ST-193 | 489416-12-8 | >98% | |
ST-193 is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, La | ||||
193209 | SPL-707 | 2195361-33-0 | >98% | |
SPL-707 is the first selective and orally active SPPL2a inhibitor. It shows adequate | ||||
193122 | SHP394 | 2055757-40-7 | >98% | |
SHP394 is a potent and orally active SHP2 inhibitor (IC50 = 23 nM) with high lipophil | ||||
193113 | SGC-GAK-1 | 2226517-76-4 | >98% | |
SGC-GAK-1 is a potent and selective GAK kinase probe which targets the ATP-binding si | ||||
19314 | SU 5214 | 186611-04-1 | >98% | |
SU 5214 is a modulator of tyrosine kinase signal transduction. | ||||
192278 | Silvestrol | 697235-38-4 | >98% | |
Silvestrol, a member of flavagline family of natural products from the genus of Aglai | ||||
192276 | Selpercatinib | 2152628-33-4 | >98% | |
Selpercatinib is a tyrosine kinase inhibitor with antineoplastic properties. | ||||
192215 | SM16 | 614749-78-9 | >98% | |
SM16 is a novel Type I TGF-β signaling inhibitor. |
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