Angiogenesis(血管生成)
- Cat.No. 产品名称 Information
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GC67940
BTK inhibitor 10
-
GC67857
(R)-Elsubrutinib
-
GC67708
PLN-1474
-
GC65909
Bexotegrast
-
GC65597
Abciximab
-
GC65529
TRAP-6 amide
A peptide PAR1 agonist
-
GC65455
c(phg-isoDGR-(NMe)k)
-
GC65439
GB-88
-
GC65312
AZ8838
-
GC64979
I-191
I-191 is a potent PAR2 antagonist that inhibits multiple PAR2-induced signaling pathways and functional responses. I-191 also inhibits ERK1/2 phosphorylation, RhoA activation, and inhibition of forskolin-stimulated cAMP accumulation induced by micromolar concentrations of biased ligand GB88.
-
GC64932
αvβ5 integrin-IN-1
-
GC64819
Elsubrutinib
-
GC64571
Sibrafiban
-
GC49882
Hemokinin 1 (human) (trifluoroacetate salt)
A peptide agonist of NK1 receptors
-
GC49873
Protectin D1 methyl ester
An esterified form of protectin D1
-
GC49808
12-methyl Tridecanoic Acid
A methylated fatty acid
-
GC49799
Apatinib-d8
An internal standard for the quantification of apatinib
-
GC64360
BTK inhibitor 18
-
GC64347
Vorapaxar sulfate
A PAR1 antagonist
-
GC64212
Valategrast hydrochloride
-
GC64120
TAK-020
-
GC63896
AS-1763
-
GC63846
BIIB091
-
GC63797
(S)-Sunvozertinib
DZD9008 (Sunvozertinib) is an oral, potent, irreversible, wild type-selective EGFR inhibitor against EGFR or HER2 Exon20ins and other mutations with IC50 ranging from 0.4 nM to 2.1 nM for mutant EGFR.
-
GC49716
Cyclo(RGDyK) (trifluoroacetate salt)
A cyclic peptide ligand of αVβ3 integrin
-
GC49713
SIKVAV (acetate)
A laminin α1-derived peptide
-
GC49686
N-desmethyl Regorafenib N-oxide
An active metabolite of regorafenib
-
GC49562
4-methoxy Estrone
An active metabolite of estrone
-
GC63658
Atopaxar
Atopaxar(E5555,ER-172594-00) is a potent, orally active, selective and reversible thrombin receptor protease-activated receptor-1 (PAR-1) antagonist.
-
GC63540
SCH79797
An antagonist of PAR1
-
GC63490
Valategrast
-
GC63232
Tolebrutinib
Tolebrutinib (SAR442168, PRN2246, BTKi'168, BTKi('168)) is an oral, CNS-penetrant, irreversible inhibitor of Bruton's tyrosine kinase (BTK) with IC50s of 0.4 nM and 0.7 nM in Ramos B cells and in HMC microglia cells, respectively.
-
GC63229
TL-895
TL-895 is a potent, orally active, ATP-competitive, and highly selective irreversible BTK inhibitor with IC50 and Ki of 1.5 nM and 11.9 nM, respectively.
-
GC62872
BMS-587101
-
GC49433
Capsiate
A capsaicin analog with diverse biological activities
-
GC49358
Sildenafil Chlorosulfonyl
An intermediate in the synthesis of sildenafil
-
GC49349
O-Desethyl Sildenafil
A metabolite of sildenafil
-
GC49221
QLT0267
An ILK inhibitor
-
GC62614
SJF620 hydrochloride
-
GC62566
αvβ1 integrin-IN-1 TFA
-
GC62515
Pirtobrutinib
A BTK inhibitor
-
GC62498
BTK inhibitor 17
-
GC62469
Protease-Activated Receptor-1, PAR-1 Agonist TFA
-
GC62397
RO0270608
-
GC62380
αvβ1 integrin-IN-1
-
GC62255
N-piperidine Ibrutinib hydrochloride
N-piperidine Ibrutinib hydrochloride, a reversible Ibrutinib derivative, is a potent BTK inhibitor with IC50s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively.
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GC62182
Echistatin TFA
-
GC62143
Carotegrast methyl
-
GC62101
PAR-2-IN-1
IUN76750 is a PAR-2 signaling pathway inhibitor.
-
GC61777
RWJ-56110 dihydrochloride