Angiogenesis - InvivoChem

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Signaling Pathways
Apoptosis
- ♦ Bcl-2(11)
- ♦ p53(11)
- ♦ Caspase(10)
- ♦ TNFa(4)
- ♦ Mdm2(15)
- ♦ c-RET(4)
- ♦ IAP(6)
- ♦ PERK(4)
- ♦ PD-1/PD-L1(11)
- ♦ Survivin(1)
PI3K/Akt/mTOR
- ♦ PI3K (62)
- ♦ Akt (19)
- ♦ mTOR (21)
- ♦ GSK-3 (17)
- ♦ ATM/ATR (0)
- ♦ PDK-1 (4)
- ♦ S6 kinase (6)
- ♦ AMPK (8)
- ♦ DNA-PK (3)
Epigenetics
- ♦ HDAC(2)
- ♦ HIF(7)
- ♦ PARP(0)
- ♦ JAK(33)
- ♦ Aurora Kinase(23)
- ♦ Histone Acetyltransferase (6)
- ♦ Histone Demethylase(10)
- ♦ Histone Methyltransferase (26)
- ♦ DNA Methyltransferase(8)
- ♦ Epigenetic Reader Domain (19)
- ♦ Sirtuin (11)
- ♦ Pim (6)
MAPK
- ♦ MEK(18)
- ♦ ERK(8)
- ♦ Raf(15)
- ♦ JNK(7)
- ♦ p38 MAPK(13)
Protein Tyrosine Kinase
- ♦ VEGFR (46)
- ♦ EGFR (40)
- ♦ PDGFR(11)
- ♦ c-MET (14)
- ♦ HER-2(2)
- ♦ ALK(10)
- ♦ FLT3 (8)
- ♦ FGFR (10)
- ♦ IFG-1R(8)
- ♦ c-Kit(3)
- ♦ Tie-2(1)
- ♦ CSF-1R(2)
- ♦ TAM Receptor (6)
- ♦ Trk receptor(3)
- ♦ c-RET(0)
Angiogenesis
- ♦ VEGFR (1)
- ♦ EGFR (0)
- ♦ PDGFR (0)
- ♦ HIF (0)
- ♦ HER-2 (0)
- ♦ JAK (0)
- ♦ FLT3 (0)
- ♦ FGFR (0)
- ♦ BTK (7)
- ♦ Syk(6)
- ♦ FAK (8)
- ♦ Src (8)
- ♦ Bcr-Abl (10)
- ♦ VDA (3)
Proteases
- ♦ Proteasome (13)
- ♦ Cysteine Protease (11)
- ♦ Serine Protease(5)
- ♦ Gamma-secretase (10)
- ♦ HCV Protease (5)
- ♦ HIV Protease(7)
- ♦ MMP (6)
- ♦ DPP-4 (8)
- ♦ Caspase (0)
NF-kB
- ♦ NOD1 (2)
- ♦ IκB/IKK(14)
- ♦ NF-κB(6)
- ♦ HDAC (0)
Autophagy
- ♦ Autophagy (20)
- ♦ LRRK2 (5)
JAK/STAT
- ♦ JAK (1)
- ♦ STAT(0)
- ♦ EGFR (0)
- ♦ Pim (0)
Metabolism
- ♦ PDE (26)
- ♦ P450 (e.g. CYP) (24)
- ♦ PPAR (16)
- ♦ Phospholipase (7)
- ♦ DHFR(5)
- ♦ Dehydrogenase (19)
- ♦ HSP (20)
- ♦ Carbonic Anhydrase (16)
- ♦ MAO (0)
- ♦ FAAH (5)
- ♦ CETP(4)
- ♦ Transferase (8)
- ♦ HMG-CoA Reductase(11)
- ♦ Hydroxylase (8)
- ♦ IDO (4)
- ♦ Retinoid Receptor (5)
- ♦ Factor Xa (4)
- ♦ AhR (3)
- ♦ Ferroptosis(3)
- ♦ Casein Kinase (4)
- ♦ NAMPT (3)
Neuronal Signaling
- ♦ 5-HT Receptor (0)
- ♦ COX (40)
- ♦ GluR (16)
- ♦ Adrenergic Receptor(0)
- ♦ AChR Receptor (47)
- ♦ Histamine Receptor (0)
- ♦ Dopamine Receptor (0)
- ♦ Opioid Receptor (0)
- ♦ GABA Receptor (0)
- ♦ P-gp (0)
- ♦ CaMK (8)
- ♦ P2 Receptor (7)
- ♦ OX Receptor (0)
- ♦ MT Receptor (0)
- ♦ BACE (2)
- ♦ Gamma-secretase (0)
- ♦ Beta Amyloid (1)
Ubiquitin
- ♦ E2 conjugating (1)
- ♦ p97 (3)
- ♦ E3 Ligase (0)
- ♦ DUB (8)
- ♦ Proteasome (0)
Stem Cells/Wnt
- ♦ Hedgehog/Smoothened ROCK (0)
- ♦ ROCK(0)
- ♦ Wnt/beta-catenin (0)
- ♦ Gamma-secretase (0)
- ♦ Casein Kinase (0)
- ♦ TGF–beta/Smad (0)
- ♦ STAT (9)
- ♦ JAK (0)
- ♦ GSK-3 (0)
DNA Damage
- ♦ Telomerase(2)
- ♦ Topoisomerase (36)
- ♦ DNA/RNA Synthesis (65)
- ♦ HDAC (38)
- ♦ ATM/ATR (14)
- ♦ PARP (28)
- ♦ Sirtuin (0)
GPCR & G Protein
- ♦ cAMP (1)
- ♦ Adenosine Receptor (4)
- ♦ Vasopressin Receptor (3)
- ♦ CXCR (3)
- ♦ CaSR (2)
- ♦ PAFR (2)
- ♦ CGRP Receptor (1)
- ♦ LPA Receptor (2)
- ♦ SGLT (4)
- ♦ S1P Receptor (7)
- ♦ Endothelin Receptor (7)
- ♦ Cannabinoid Receptor (7)
- ♦ 5-HT Receptor (63)
- ♦ Adrenergic Receptor (65)
- ♦ Histamine Receptor (41)
- ♦ Dopamine Receptor (28)
- ♦ Opioid Receptor (9)
- ♦ Hedgehog/Smoothened ROCK (11)
- ♦ OX Receptor (7)
- ♦ MT Receptor (2)
TGF-beta/Smad
- ♦ MT Receptor (20)
- ♦ Bcr-Abl (0)
- ♦ ROCK (20)
- ♦ PKC (9)
Cell Cycle
- ♦ CDK (38)
- ♦ Rho (13)
- ♦ PLK (10)
- ♦ Chk (6)
- ♦ Aurora Kinase (0)
- ♦ ROCK (0)
- ♦ PD-1/PD-L1 (0)
- ♦ c-Myc (2)
- ♦ Wee1 (1)
- ♦ APC (1)
Cytoskeletal Signaling
- ♦ Bcr-Abl(1)
- ♦ Wnt/beta-catenin (10)
- ♦ PKC (0)
- ♦ FAK(0)
- ♦ HSP (0)
- ♦ Dynamin (3)
- ♦ PAK (3)
- ♦ Integrin (8)
- ♦ Microtubule Associated(25)
- ♦ Kinesin (6)
Transmembrane
- ♦ P-gp (6)
- ♦ Proton Pump (10)
- ♦ GABA Receptor (11)
- ♦ Sodium Channel (27)
- ♦ Potassium Channel (16)
- ♦ Calcium Channel (33)
- ♦ ATPase (0)
- ♦ CRM1 (1)
- ♦ TRPV (0)
- ♦ CFTR (0)
- ♦ OCT (0)
Endocrinology & Hormones
- ♦ Opioid Receptor (0)
- ♦ Glucocorticoid Receptor(5)
- ♦ Estrogen/progestogen Receptor (34)
- ♦ Androgen Receptor (13)
- ♦ RAAS (27)
- ♦ Aromatase(5)
- ♦ GPR(5)
- ♦ 5-alpha Reductase (2)
Microbiology
- ♦ HCV Protease (0)
- ♦ HIV Protease (0)
- ♦ CCR (1)
- ♦ Reverse Transcriptase(27)
- ♦ Integrase (0)
Others
- ♦ gp120/CD4 (2)
- ♦ FXR(4)
- ♦ PKA (2)
- ♦ Thrombin (4)
- ♦ Liver X receptor (3)
- ♦ IL Receptor (0)
- ♦ Others 1(362)
- ♦ Others 2(433)
- ♦ Others 3(331)
- ♦ Others 4(295)
- ♦ Others 5(250)
- ♦ Others 6(466)
- ♦ Others 7(230)
New Products
- ♦ New1(25677)
- ♦ New2(6771)
- ♦ New3(1062)

Product Type
Natural Products
- ♦ Natural Products 1(443)
Peptides
- ♦ Peptides 1(1957)
Antibodies
Amino Acids
- ♦ Amino Acids 1(384)
PROTACs
- ♦ PROTACs 1(29)
Fine Intermediates/Building Blocks
Others

Bulletin Board

ALG1001 (Risuteganib; Luminate)

Catalog No： V0194

CAS No. (CAS Registry Number)： 1307293-62-4

Price： $0/g

Description: ALG1001 (discontinued, also known as Risuteganib and Luminate, developed by Allegro Ophthalmics) is a potent and selective small peptide with a sequence of Gly-Arg-Gly...

Ibrutinib (PCI-32765)

Catalog No： V0643

CAS No. (CAS Registry Number)： 936563-96-1

Price： $0/g

Description: Ibrutinib (formerly PCI32765; trade name Imbruvica), an approved anticancer drug, is a covalent/irreversible and orally bioavailable Brutons tyrosine kinase (Btk) inhibitor...

Spebrutinib (CC292; AVL292)

Catalog No： V0644

CAS No. (CAS Registry Number)： 1202757-89-8

Price： $0/g

Description: Spebrutinib (formerly AVL-292; CC-292; SBT) is a covalent/irreversible, orally bioactive, and highly selective inhibitor of Bruton's agammaglobulinemia tyrosine kinase/BTK inhibitor w...

CNX-774

Catalog No： V0645

CAS No. (CAS Registry Number)： 1202759-32-7

Price： $0/g

Description: CNX-774 (CNX774) is an irreversible/covalent, orally bioavailable, and highly selective inhibitor of BTK (Bruton's tyrosine kinase) with potential anticancer activity. It inhibits BTK...

CGI1746

Catalog No： V0646

CAS No. (CAS Registry Number)： 910232-84-7

Price： $0/g

Description: CGI1746 (CGI-1746) is a reversible/non-covalent and highly selective small-molecule inhibitor of the Bruton's tyrosine kinase-Btk with potential anti-inflammatory activity. It inhibit...

LFM-A13

Catalog No： V0647

CAS No. (CAS Registry Number)： 244240-24-2

Price： $0/g

Description: LFM-A13 (LFM-A1-3) is a novel, potent and specific Bruton's tyrosine kinase (BTK) inhibitor with potential anticancer activity. It inhibits BTK with an IC50 of 2.5 μM, and shows 100-f...

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