Others 15

ADC Related

ADC Antibody ADC Cytotoxin ADC Linker ADCs Drug-Linker Conjugates for ADC
Angiogenesis

5-alpha Reductase ALK Bcr-Abl BTK EGFR FAK FLT3 HER-2 HIF Src Syk VDA VEGFR
Anti-infection

Antibiotic Arenavirus Bacterial CMV EBV Enterovirus Filovirus Fungal Gli HBV HCV HCV Protease HIV HSV Influenza Virus Parasite RABV Reverse Transcriptase RSV SARS-CoV TMV Virus Protease
Apoptosis

Apoptosis ASK Bcl-2 Caspase c-Myc c-RET Cytohesin DAPK Ferroptosis FKBP IAP Mdm2 p53 PD-1 PD-L1 PERK PKD Ras RIP kinase ROS Survivin Thymidylate Synthase TNF Receptor TNFa TRADD
Autophagy

Autophagy LRRK2 Mitophagy OGA ULK
Cell Cycle

Antifolate APC Aurora Kinase BMI-1 CDK Chk c-Myc Eukaryotic Initiation Factor G-quadruplex HDAC HSP Kinesin LIMK Mad2 Microtubule(Tubulin) Mps1 Nucleoside Antimetabolite/Analog Nur77 p21 PAK PERK PFKFB PLK PPAR Ras Rho ROCK SRPK TOPK Topoisomerase Wee1
Cytoskeletal Signaling

Arp2 3 Complex Bcr-Abl Cardiac Myosin Dynamin Gap Junction Protein HSP Integrin Kinesin Microtubule Associated MLCK Myosin PAK TACC3 Wntbeta-catenin
DNA Damage

ATM(ATR) CRISPR(Cas9) DNA alkylator DNA Stain DNA(RNA) Synthesis GAK HDAC HSP Nucleoside Antimetabolite(Analog) OGG1 p97 PARG PARP RAD51 RNR Sirtuin SMN Telomerase Topoisomerase
Endocrinology & Hormones

5-alpha Reductase ACE Adrenergic Receptor Androgen Receptor Aromatase Estrogenprogestogen Receptor Glucocorticoid Receptor GPR Mineralocorticoid Receptor RAAS THR TSH Receptor
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain EZH1 2 HDAC HIF Histone Acetyltransferase Histone Demethylase Histone Methyltransferase JAK MAT MicroRNA MLL Pim PKC Protein Arginine Deiminase Sirtuin Small Interfering RNA (siRNA) SMYD

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Others 15

Others 15 related products

Cat No.	Product Name	CAS No.	Product Description
V92227	Methyl 9(S),10(R)-epoxy-13(S)-hydroxy-11(E)-octadecenoate	71201-26-8	Methyl 9(S),10(R)-epoxy-13(S)-hydroxy-11(E)-octadecenoate is an ester product.
V92346	Methyl cis-12-octadecenoate	2733-86-0	Methyl cis-12-octadecenoate is an oleic acid derivative obtained by Witting reaction and can be used for human metabolism studies.
V92224	Methyl cis-9,10-methylenehexadecanoate	36254-90-7	Methyl cis-9,10-methylenehexadecanoate is an ester product.
V90033	Methyl Red sodium salt	845-10-3	Methyl Red sodium salt is a biomaterial or organic compound that can be used in life science research.
V89443	Methyl-4-oxoretinoate	38030-58-9	Methyl-4-oxoretinoate is a derivative of retinoic acid.
V92045	Methylbiocin	23370-12-9	Methylbiocin is an ATP-competitive inhibitor of human CMG helicase (hCMG helicase) with IC50 of 59 µM.
V89382	Metoxadiazone	60589-06-2	Metoxadiazone is an insecticide that is effective against a wide range of insect species, including cockroaches and ants.
V89735	Metronidazole/BSA		Metronidazole/BSA is an antigen-adjuvant conjugate of metronidazole conjugated to bovine serum albumin (BSA).
V89746	Metronidazole/KLH		Metronidazole/KLH is an antigen-adjuvant conjugate of metronidazole conjugated to hemocyanin (KLH).
V88905	METTL3-IN-7		METTL3-IN-7 (F039-0002) is a potent METTL3 inhibitor.
V88904	METTL3-IN-8	932512-38-4	METTL3-IN-8 (7460-0250) is a potent METTL3 inhibitor.
V92577	MFCD30718058	1621274-17-6
V92585	MFCD31707644	1810068-35-9
V91161	mgc(3Me)JF549		mgc(3Me)JF549 is a Golgi probe with an excitation wavelength of 561 nm.
V89426	Mianserin impurity-1	73771-03-6	Mianserin impurity-1 is a reference substance for mianserin impurity.
V86987	MIP-1095 TFA		MIP-1095 (RPS-001) TFA is an effective inhibitor of PSMA with good biodistribution rate and can efficiently target tumor lesions.
V89275	MK-6240 Precursor	1841444-11-8	MK-6240 Precursor (6e) is a precursor for the synthesis of (18)F]-MK-6240.
V91845	MMA-NODAGA	1440903-11-6	MMA-NODAGA is a chelating agent used for site-specific labeling of target proteins containing unpaired cysteines.
V89788	MNI-caged-L-glutamate TFA	2226362-29-2	MNI-caged-L-glutamate TFA is a reagent that can quickly and effectively release neuroactive amino acids.
V91849	Moxilubant	146978-48-5	Moxilubant (CGS-25019C;LTB-019) is an orally active BLT1 antagonist that inhibits LTB4 signaling with a potency of 2 ~ 4 nM.