Login
Contact us
0
Search
Toggle navigation
About
About Hodoodo
Contact Hodoodo
About Hodoodo Products
Careers at Hodoodo
Licensing
Remove your patented product from our web
Products
Browse all products
Browse products by research area
Newest stocked products
Featured products
Services
Custom Synthesis
Frequently asked questions
Process Research & Development
Ordering
How To Order
Terms and Conditions
Request Quote
Privacy Policy
Resources
News
Elemental Period Table
Download Hodoodo Catalogues
Amino Acid Nomenclature Guide
Useful Free Databases
NMR Chemical Shifts of Impurities Charts
Drug Synthesis
Structure search
All Products
Featured Products
Newest Products
Research Areas
16
Angiogenesis
Bcr-Abl
BTK
EGFR
FAK
FGFR
FLT3
HIF
JAK
PDGFR
Src
Syk
VDA
VEGFR
Bcl-2
test3
demo333
8
Apoptosis
Caspase
c-RET
IAP
Mdm2
p53
PERK
Survivin
TNF-alpha
2
Autophagy
LRRK2
APC
9
Cell Cycle
Aurora Kinase
CDK
Chk
c-Myc
PLK
Rho
ROCK
Wee1
Akt
11
Cytosketetal Signaling
Bcr-Abl
Dynamin
FAK
HSP
Integrin
Kinesin
Microtubule
PAK
PKC
Wnt/beta-catenin
ATM/ATR
8
DNA Damage
DNA/RNA Synthesis
DNA-PK
HDAC
PARP
Sirtuin
Telomerase
Topoisomerase
5-alpha Reductase
8
Endocrinology & Hormones
Androgen Receptor
Aromatase
Estrogen/progestogen Receptor
Glucocorticoid Receptor
GPR
Opioid Receptor
RAAS
Aurora Kinase
12
Epigenetics
DNA Methyltransferase
Epigenetic Reader Domain
HDAC
HIF
Histone Acetyltransferase
Histone Demethylase
Histone Methyltransferase
JAK
PARP
Pim
Sirtuin
5-HT Receptor
19
GPCR & G Protein
Adenosine Receptor
Adrenergic Receptor
cAMP
Cannabinoid Receptor
CaSR
CGRP Receptor
CXCR
Dopamine Receptor
Hedgehog/Smoothened
Histamine Receptor
LPA Receptor
MT Receptor
Opioid Receptor
OX Receptor
PAFR
S1P Receptor
SGLT
Vasopressin Receptor
EGFR
4
JAK/STAT
JAK
Pim
STAT
ERK
5
MARK
JNK
MEK
p38 MAPK
Raf
ATPase
10
Transmembrane Transporters
Calcium Channel
CFTR
CRM1
GABA Receptor
P-gp
Potassium Channel
Proton Pump
Sodium Channel
TRPV
AhR
20
Metabolism
Carbonic Anhydrase
CETP
Dehydrogenase
DHFR
FAAH
Factor Xa
Ferroptosis
HMG-CoA Reductase
HSP
Hydroxylase
IDO
MAO
P450 (e.g. CYP17)
PDE
Phospholipase (e.g. PLA)
PPAR
Procollagen C Proteinase
Retinoid Receptor
Transferase
CCR
5
Microbiology
HCV Protease
HIV Protease
Integrase
Reverse Transcriptase
5-HT Receptor
17
Neuronal Signaling
AChR
Adrenergic Receptor
BACE
Beta Amyloid
CaMK
COX
Dopamine Receptor
GABA Receptor
Gamma-secretase
GluR
Histamine Receptor
MT Receptor
Opioid Receptor
OX Receptor
P2 Receptor
P-gp
HDAC
4
NF-kB
IκB/IKK
NF-κB
NOD1
Akt
9
PI3K/AKT/mTOR
AMPK
ATM/ATR
DNA-PK
GSK-3
mTOR
PDK-1
PI3K
S6 Kinase
Caspase
9
Proteases
Cysteine Protease
DPP-4
Gamma-secretase
HCV Protease
HIV Protease
MMP
Proteasome
Serine Protease
ALK
16
Protein Tyrosine Kinase
c-Kit
c-Met
c-RET
CSF-1R
EGFR
Ephrin Receptor
FGFR
FLT3
HER2
IGF-1R
PDGFR
TAM Receptor
Tie-2
Trk Receptor
VEGFR
Gamma-secretase
8
Stem Cells / Wnt
GSK-3
Hedgehog/Smoothened
JAK
ROCK
STAT
TGF-beta/Smad
Wnt/beta-catenin
Bcr-Abl
4
TGF-beta /Smad
KC
ROCK
TGF-beta
DUB
5
Ubiquitin
E1 Activating
E2 Conjugating
E3 Ligase
p97
Proteasome
2
Lipid reagent
All lipid reagent
Ionizable lipid
2
Photodynamic therapy
Photodynamic Therapy (PDT)
Porphyrin
Products starting with 'Z'
or product name starting with:
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
« First
‹ Prev
1
...
5
6
7
8
9
...
14
Next ›
Last »
H121011
ZXH-4-137
ZXH-4-137 is a PROTAC compound.
H121010
ZXH-4-130
ZXH-4-130 is a PROTAC compound.
H208314
Z640
Z640 an aPKC agonist. Z640 was further confirmed as a non‑selective aPKC agonist that can activate t…
H208309
ZLD2218
ZLD2218 exhibited the most potent inhibitory activity against BRD4, with the IC50 value of 107 nM, w…
H471195
ZUN04395
featured
ZUN04395, also known as GSK3β inhibitor XI, is a potent inhibitor of glycogen synthase kinase 3β.
H208215
ZAP70-IN-10t
ZAP70-IN-10t is a biochemical
H208212
ZAP70-IN-11
ZAP70-IN-11 is essential for T-cell antigen recognition, and propagate signals from the T-cell recep…
H208188
ZLWH-23
ZLWH-23 displayed efficient reduction against tau hyperphosphorylation on Ser-396 site in Tau (P301L…
H208156
Z56965384
H556104
ZD7114 HCl
ZD7114, also known as ICI-D7114, is a selective adrenoceptor agonist of brown fat and thermogenesis.…
H466275
ZN-3-80
ZN-3-80 is a SARS-CoV-2 PLpro Inhibitor.
H208091
ZE132
featured
ZE132 is a novel potent PD-1/PD-L1 interaction inhibitor that promotes cytotoxic T-cell tumour infil…
H208063
Z4446724338
Z4446724338 is a novel potent dual σ1/2 ligand.
H208062
Z1241145220
Z1241145220 is a novel potent ligand.
H208043
ZB-R-55
ZB-R-55 is a Potent and Selective RIPK1 Inhibitor. ZB-R-55 targets Dual-Pockets for the Treatment o…
H208001
Zn-HTSM
Zn-HTSM is a novel antidiabetic agent for the treatment of type 2 diabetes mellitus (DM).
H466152
ZYDPLA1
ZYDPLA1 is a novel next generation orally active DPP-4 inhibitor to treat Type 2 Diabetes.
H471138
ZD 7155 hydrochloride
featured
ZD 7155 hydrochloride is a potent selective Angiotensin II AT1 antagonist.
H466081
ZG-2033
ZG-2033 is a Novel Potent and Orally Bioavailable Hypoxia-Inducible Factor 2α (HIF-2α) Agonist.
H465982
Zuvotolimod
Zuvotolimod is a biochemical.
H465973
Zilurgisertib
Zilurgisertib is a serine/threonine kinase inhibitor.
H465972
Zevaquenabant
Zevaquenabant , also known as MRI-1867, is a cannabinoid 1 (CB1) receptor antagonist. MRI-1867 is a…
H465971
Zagociguat
Zagociguat is a guanylate cyclase activator.
H465890
ZM241358
ZM241358 is a selective A2A and dual A2A/A1 AR antagonist.
H465822
Z-505
Z-505 is a GHS-R1a ligand.
H471109
ZZW-115 HCl
featured
ZZW-115 HCl is a potent NUPR1 inhibitor. ZZW-115 induces ferroptosis in a mitochondria-dependent man…
H465812
ZB-S-29
ZB-S-29 is a highly efficient SHP2 degrader with a DC50 of 6.02 nM. ZB-S-29 effectively induced the …
H207172
Zunsemetinib
new
featured
Zunsemetinib, also known as ATI-450 and CDD450, is a potent MK2 Inhibitor. ATI-450 binds with high a…
H465743
ZL0590
ZL0590 is a Bromodomain-containing Protein 4 (BRD4) BD1 Inhibitor. ZL0590 targeting a unique, previ…
H465724
ZFH7116
ZFH7116 is a TMPRSS2 inhibitor that potently block SARS-CoV-2 and MERS-CoV viral entry and protect h…
H555051
ZZW-115
new
featured
ZZW-115 is a potent NUPR1 inhibitor. ZZW-115 induces ferroptosis in a mitochondria-dependent manner.…
H465661
ZL3138
ZL3138 is a novel β-catenin/B-cell lymphoma 9 (BCL9) inhibitor, disrupting the β-catenin/BCL9 protei…
H465648
ZG-2006
ZG-2006 is a PHD inhibitor and HIF-2α agonist.
H556040
Zotizalkib
new
featured
Zotizalkib, also known as TPX-0131, is a Potent CNS-penetrant, Next-generation Inhibitor of Wild-typ…
H465630
ZHX-2-45
ZHX-2-45 is a CRBN-based PROTAC.
H465583
ZINC03830212
ZINC03830212 is a SIRT3 activator.
H414734
Ziftomenib
Ziftomenib, also known as KO539, is an orally bioavailable inhibitor of the menin-mixed lineage leuk…
H414733
zifanocyclinum
zifanocyclinum is a tetracycline antibiotic
H414732
zectivimodum
zectivimodum is an immunomodulator
H414731
zavacorilantum
zavacorilantum is a glucocorticoid receptor antagonist
H414730
Zastaprazan
featured
Zastaprazan, also known as JP-1366, is a proton pump inhibitor. JP-1366 mediates strong, selective, …
H5560172
ZINC65362194
ZINC65362194 is a potential bioactive molecule.
H465355
ZY12201
ZY12201 is a novel potent and orally bioavailable TGR5 agonist.
H465332
ZW4864
ZW4864 is an Orally Bioavailable Small-Molecule Inhibitor for the β‑Catenin/B-Cell Lymphoma 9 Protei…
H414654
Zolamine HCl
Zolamine HCl is an Antihistaminic and Topical Anesthetic
H464993
Z-FR-AMC TFA
featured
Z-FR-AMC is a fluorogenic substrate for cathepsin L. Upon enzymatic cleavage by cathepsin L, 7-amino…
H464940
ZSN-76403
featured
ZSN-76403 is an inhibitor of the cytochrome P450 (CYP) isoform CYP2C19 (Ki = 0.25 µM). It is selecti…
H577032
Zifrosilone
Zifrosilone is an acetylcholinesterase inhibitor.
H576994
Zindotrine
Zindotrine is a bronchodilator.
H464828
Zingibroside R1
featured
Zingibroside R1 is a triterpene saponin and an active metabolite of ginsenoside Ro that has been fou…
« First
‹ Prev
1
...
5
6
7
8
9
...
14
Next ›
Last »