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Carbonic Anhydrase
Signaling Pathways
Apoptosis
♦
Bcl-2
(
10
)
♦
p53
(
11
)
♦
Caspase
(
10
)
♦
TNFa
(
4
)
♦
Mdm2
(
14
)
♦
c-RET
(
4
)
♦
IAP
(
6
)
♦
PERK
(
4
)
♦
PD-1/PD-L1
(
11
)
♦
Survivin
(
1
)
PI3K/Akt/mTOR
♦
PI3K
(
62
)
♦
Akt
(
18
)
♦
mTOR
(
21
)
♦
GSK-3
(
17
)
♦
ATM/ATR
(
0
)
♦
PDK-1
(
4
)
♦
S6 kinase
(
6
)
♦
AMPK
(
8
)
♦
DNA-PK
(
3
)
Epigenetics
♦
HDAC
(
2
)
♦
HIF
(
8
)
♦
PARP
(
0
)
♦
JAK
(
33
)
♦
Aurora Kinase
(
23
)
♦
Histone Acetyltransferase
(
6
)
♦
Histone Demethylase
(
9
)
♦
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
(
1
)
♦
FAK
(
0
)
♦
HSP
(
0
)
♦
Dynamin
(
3
)
♦
PAK
(
3
)
♦
Integrin
(
8
)
♦
Microtubule Associated
(
24
)
♦
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
(
359
)
♦
Others 2
(
433
)
♦
Others 3
(
330
)
♦
Others 4
(
296
)
♦
Others 5
(
250
)
♦
Others 6
(
233
)
♦
Others 7
(
229
)
New Products
♦
New1
(
29061
)
♦
New2
(
3627
)
♦
New3
(
862
)
Product Type
Natural Products
♦
Natural Products 1
(
444
)
Peptides
♦
Peptides 1
(
1998
)
Antibodies
Amino Acids
♦
Amino Acids 1
(
389
)
PROTACs
♦
PROTACs 1
(
40
)
Fine Intermediates/Building Blocks
Others
Dorzolamide HCl
Catalog No:
V0893
CAS No. (CAS Registry Number):
130693-82-2
Price:
$0/g
Description: Dorzolamide HCl (also known as MK-507, or L-671152 HCl; L671152; MK507; trade name Trusopt) is a water-soluble, potent inhibitor of human carbonic anhydrase II and IV with Ki of 1.9 ...
Topiramate
Catalog No:
V0894
CAS No. (CAS Registry Number):
97240-79-4
Price:
$0/g
Description: Topiramate (also known as MCN 4853, RWJ 17021) is a novel, potent, anticonvulsant (antiepilepsy) drug and is a mutil-targeted inhibitor that has been r...
U-104
Catalog No:
V0895
CAS No. (CAS Registry Number):
178606-66-1
Price:
$0/g
Description: U-104 (also known as MST-104, SLC-0111 and NSC 213841) is a novel and potent inhibitor of transmembrane carbonic anhydrase (CA) with Ki of 45.1 nM and 4.5 nM for CA IX and CA XII, re...
Tioxolone
Catalog No:
V0896
CAS No. (CAS Registry Number):
4991-65-5
Price:
$0/g
Description: Tioxolone is a potent metalloenzyme carbonic anhydrase I inhibitor with a Ki of 91 NM. Tioxolone is reported to possess cytostatic, antipsoriatic, antibacterial and anti-mycotic propertie...
Methocarbamol
Catalog No:
V0897
CAS No. (CAS Registry Number):
532-03-6
Price:
$0/g
Description: Methocarbamol (formerly also known as AHR 85) is a potent carbonic anhydrase inhibitor, and is used as a central muscle relaxant to treat skeletal muscle spasms. This compound i...
Brinzolamide
Catalog No:
V0898
CAS No. (CAS Registry Number):
138890-62-7
Price:
$0/g
Description: Brinzolamide (formerly also known as AL-4862) is a highly potent and selective carbonic anhydrase II inhibitor with IC50 of 3.19 nM. References: Surv Ophthalmol. 2000 ...
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