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Results for "

HL60

" in MedChemExpress (MCE) Product Catalog:

By Targets:	ADC Cytotoxin (5) Akt (1) AMPK (1) Angiotensin-converting Enzyme (ACE) (1) Antibiotic (4) Apoptosis (35) Autophagy (10) Bacterial (7) Bcl-2 Family (1) Bombesin Receptor (1) c-Myc (3) Calcium Channel (1) Cannabinoid Receptor (1) Casein Kinase (1) Caspase (2) Cathepsin (1) CDK (1) Cuproptosis (1) Cytochrome P450 (1) DNA Alkylator/Crosslinker (2) DNA Methyltransferase (1) DNA-PK (1) DNA/RNA Synthesis (10) Drug-Linker Conjugates for ADC (1) EBI2/GPR183 (1) Endogenous Metabolite (9) Epigenetic Reader Domain (1) Farnesyl Transferase (1) Filovirus (1) FLT3 (1) Fungal (1) Glucosylceramide Synthase (GCS) (1) Glyoxalase (GLO) (1) GSK-3 (1) HDAC (3) Histone Acetyltransferase (1) Histone Methyltransferase (1) HIV (2) HSP (1) Integrin (2) Interleukin Related (3) Isotope-Labeled Compounds (3) Lipoxygenase (2) Microtubule/Tubulin (2) mTOR (1) NO Synthase (1) Orthopoxvirus (4) P-glycoprotein (2) Parasite (3) PI3K (2) PKC (3) Polo-like Kinase (PLK) (1) RAR/RXR (1) Reactive Oxygen Species (2) Serotonin Transporter (6) Topoisomerase (4) VD/VDR (2) Xanthine Oxidase (1) β-catenin (1)
By Research Areas:	Cancer (102) Cardiovascular Disease (1) Infection (17) Inflammation/Immunology (18) Metabolic Disease (5) Neurological Disease (7)

By Targets:

ADC Cytotoxin (5)

Akt (1)

AMPK (1)

Angiotensin-converting Enzyme (ACE) (1)

Antibiotic (4)

Apoptosis (35)

Autophagy (10)

Bacterial (7)

Bcl-2 Family (1)

Bombesin Receptor (1)

c-Myc (3)

Calcium Channel (1)

Cannabinoid Receptor (1)

Casein Kinase (1)

Caspase (2)

Cathepsin (1)

CDK (1)

Cuproptosis (1)

Cytochrome P450 (1)

DNA Alkylator/Crosslinker (2)

DNA Methyltransferase (1)

DNA-PK (1)

DNA/RNA Synthesis (10)

Drug-Linker Conjugates for ADC (1)

EBI2/GPR183 (1)

Endogenous Metabolite (9)

Epigenetic Reader Domain (1)

Farnesyl Transferase (1)

Filovirus (1)

FLT3 (1)

Fungal (1)

Glucosylceramide Synthase (GCS) (1)

Glyoxalase (GLO) (1)

GSK-3 (1)

HDAC (3)

Histone Acetyltransferase (1)

Histone Methyltransferase (1)

HIV (2)

HSP (1)

Integrin (2)

Interleukin Related (3)

Isotope-Labeled Compounds (3)

Lipoxygenase (2)

Microtubule/Tubulin (2)

mTOR (1)

NO Synthase (1)

Orthopoxvirus (4)

P-glycoprotein (2)

Parasite (3)

PI3K (2)

PKC (3)

Polo-like Kinase (PLK) (1)

RAR/RXR (1)

Reactive Oxygen Species (2)

Serotonin Transporter (6)

Topoisomerase (4)

VD/VDR (2)

Xanthine Oxidase (1)

β-catenin (1)

By Research Areas:

Cancer (102)

Cardiovascular Disease (1)

Infection (17)

Inflammation/Immunology (18)

Metabolic Disease (5)

Neurological Disease (7)

124

Inhibitors & Agonists

Fluorescent Dye

Peptides

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Sophoraflavanone G 1 Publications Verification Kushenol F	Apoptosis	Cancer
Sophoraflavanone G (Kushenol F) is iaolated from Sophora flavescens and shows anti-tumor and anti-inflammatory properties. Sophoraflavanone G (Kushenol F) induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related pathways .

Neolancerin	Others	Cancer
Neolancerin is a natural product with weak cytotoxic activity against HL-60 cells .

Lepidiline A	Others	Cancer
Lepidiline A shows cytotoxic activity against HL-60 cells with an IC₅₀ of 32.3 μM.

Theasaponin E2	Others	Cancer
Theasaponin E2 shows cytotoxicity against K562 and HL60 cells (IC₅₀: 14.7 μg/mL). Theasaponin E2 can be isolated from Camellia sinensis .

Yadanziolide C	Others	Cancer
Yadanziolide C is a quassinoid with antiproliferative and differentiation-inducing properties in promyelocytic HL-60 cells .

c-Myc inhibitor 14	c-Myc	Cancer
c-Myc inhibitor 14 (Compound 13A) is a c-Myc protein inhibitor. The IC₅₀ value of HL60 inhibitor is <100 nM. c-Myc inhibitor 14 shows antitumor activity .

Lepidiline C	Others	Cancer
Lepidiline C shows cytotoxic activity against HL-60 cells with an IC₅₀ of 27.7 μM.

Caspase-3 activator 3	Caspase Apoptosis	Cancer
Caspase-3 activator 3 (compound 2h) induces apoptosis in HL-60 and K562 cells via significant caspase 3 activation. Caspase-3 activator 3 shows antileukemic acticity against HL-60 and K562 cells, with IC₅₀ values of 42.89 and 33.61 μM, respectively .

Isolupalbigenin	NO Synthase	Inflammation/Immunology
Isolupalbigenin is an inhibitor of NO. Isolupalbigenin has anti-proliferative activity on HL-60 cells with an IC₅₀ of 5.1 μM .

Ustusolate E	Others	Cancer
Ustusolate E is a drimane sesquiterpene with moderate cytotoxicity against HL-60 cells with an IC₅₀ value of 9.0 μM .

Nordalbergin	Others	Cancer
Nordalbergin, a coumarin isolated from the wood bark of Dalbergia sissoo. Nordalbergin shows strong activity in the induction of differentiation of HL-60 .

Viteralone (S)-Viteralone	Others	Cancer
Viteralone (compound 5) is a natural product that can be isolated from Vitex negundo. Viteralone is cytotoxic to HL-60 cancer cells .

Trigoxyphin A	Others	Cancer
Trigoxyphin A is a oxygenated daphnane-type diterpenoids. Trigoxyphin A exhibites strong cytotoxic activity against HL60 and A549 with IC₅₀s of 0.27 and 7.5 μM, respectively .

Ginsenoside F5	Apoptosis	Cancer
Ginsenoside F5, from crude extracts of flower buds of Panax ginseng, remarkably inhibits the growth of HL-60 cells by the apoptosis pathway .

Trimidox VF-233	DNA/RNA Synthesis	Cancer
Trimidox (VF-233) is a ribonucleotide reductase inhibitor with antileukemic activities. Trimidox inhibits the growth of human promyelocytic leukemia HL-60 cells with an IC₅₀ of 35 μM .

Trimidox hydrochloride VF-233 hydrocHLoride	DNA/RNA Synthesis	Cancer
Trimidox hydrochloride (VF-233) is a ribonucleotide reductase inhibitor with antileukemic activities. Trimidox hydrochloride inhibits the growth of human promyelocytic leukemia HL-60 cells with an IC₅₀ of 35 μM .

Epinodosin	Others	Infection Inflammation/Immunology
Epinodosin is a diterpenoid. Epinodosin has moderate cytotoxicity against HL-60 cells with IC₅₀ value of 10.4 μM. Epinodosin can be used for the research of inflammatory diseases .

Shikokianin	Others	Cancer
Shikokianin, a diterpenoid, shows significant cytotoxicity against HL-60 and A-549 cells with IC₅₀ values of 3.4 μM and 18.8 μM, respectively .

BrBzGCp2 S-p-Bromobenzylglutathione cyclopentyl diester	Glyoxalase (GLO)	Neurological Disease Cancer
BrBzGCp2 is a Glyoxalase 1 (GLO1) inhibitor, with a GC₅₀ of 4.23 μM in HL-60 cells. BrBzGCp2 possesses antitumor and neuroprotective activity .

PAO-Nap	Apoptosis	Cancer
PAO-Nap is the modified PAO attached a naphthalimide fluorophore using aminocaproic acid as a linker. PAO induces oxidative stress-mediated apoptosis in HL-60 cells by selectively targeting thioredoxin reductase .

Lewis a trisaccharide Lewis a	Others	Others
Lewis a trisaccharide (Lewis a) is a trisaccharide that has been found to be present in the glycan structures of spermatozoa. Lewis a trisaccharide also is a major component of the glycan structures on the surface of HL-60 cells .

S-(N-PhenethylthiocarbaMoyl)-L-cysteine PEITC-Cys	DNA/RNA Synthesis Cytochrome P450	Cancer
S-(N-PhenethylthiocarbaMoyl)-L-cysteine (PEITC-Cys), an anticarcinogenic agent, has antileukemic activity. S-(N-PhenethylthiocarbaMoyl)-L-cysteine inhibits DNA synthesis in HL60 cells . S-(N-PhenethylthiocarbaMoyl)-L-cysteine is a P450 inhibitor .

Clofilium tosylate
Clofilium tosylate, a potassium channel blocker, induces apoptosis of human promyelocytic leukemia (HL-60) cells via Bcl-2-insensitive activation of caspase-3. Antiarrhythmic agent .

(S)-Erypoegin K	Apoptosis	Cancer
(S)-Erypoegin K is a potent anticancer agent. (S)-Erypoegin K shows potent anti-proliferative activity against HL-60 cells. (S)-Erypoegin K induces apoptosis .

Norglaucine (+)-Norglaucine	Others	Cancer
Norglaucine ((+)-Norglaucine), a cytotoxic alkaloid, exhibits cytotoxicity towards the tumor cell lines B16-F10, HepG2, K562 and HL-60 cells .

Aspochalasin M	Others	Cancer
Aspochalasin M is a colorless solid. Aspochalasin M shows modest activity against HL-60 cells with an IC₅₀ of 20.0 μM. Aspochalasin M has the potential for the research of leukemic disease .

Piptocarphin F	Others	Cancer
Piptocarphin F (Compound 5) is a sesquiterpene lactone. Piptocarphin F shows cytotoxic activity on human leukemia cell line HL-60 (IC₅₀=5.69 μmol*L ^-1) .

Eupalinolide B	Others	Cancer
Eupalinolide B is a germacrane sesquiterpene isolated from Eupatorium lindleyanum. Eupalinolide B demonstrates potent cytotoxicity against A-549, BGC-823 and HL-60 tumour cell lines .

Pulchinenoside E2	Others	Cancer
Pulchinenoside E2 (Compound 8) is a triterpene saponin isolated from the roots of Pulsatilla chinensis. Pulchinenoside E2 shows cytotoxic to HL-60 cells with an IC₅₀ value of 2.6 µg/mL .

Glaucocalyxin B	Autophagy	Cancer
Glaucocalyxin B is an ent kaurane diterpenoid isolated from the Chinese traditional medicine Rabdosia japonica with anticancer and antitumor activity; decreases the growth of HL-60 cells with an IC₅₀ of approximately 5.86 μM at 24 h.

2,3-O-Isopropylidenyl euscaphic acid	Others	Cancer
2,3-O-Isopropylidenyl euscaphic acid, a triterpenoid from the seeds of blackberry (Rubus fructicosus), exhibits cytotoxic activity towards HL-60 human leukaemia cells with IC₅₀ value of 72.8 μM .

Viscidulin III Ganhuangenin	Others	Cancer
Viscidulin III is a compound isolated from the roots of Scutellaria planipes (L.) . Viscidulin III can inhibit the proliferation of HL-60 (IC50= 17.4μM). Viscidulin III is a potential natural tumor inhibitor .

6-Formylpterin	Xanthine Oxidase Apoptosis Reactive Oxygen Species	Metabolic Disease
6-Formylpterin is an inhibitor of Xanthine Oxidase. 6-Formylpterin induces intracellular ROS generation and apoptosis in HL-60 cells. 6-Formylpterin suppresses cell proliferation in PanC-1 cells .

4-Bromo A23187	Calcium Channel Bacterial Apoptosis Antibiotic	Infection Cancer
4-Bromo A23187 is a halogenated analog of the highly selective calcium ionophore A-23187. 4-Bromo A23187, a calcium modulator, induces apoptosis in different cells, including HL-60 cells .

6β,7β-Epoxyasteriscunolide A	Others	Cancer
6β,7β-Epoxyasteriscunolide A, a sesquiterpenoid, shows cytotoxicity against the HL-60 and MOLT-3 leukemia cell lines, with IC₅₀s range 4.1-5.4 μM .

Salvinolone	Bacterial	Inflammation/Immunology Cancer
Salvinolone is active against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). Salvinolone shows cytotoxic activity with an IC₅₀ of 47.6 μM against the HL-60 tumor cell line for 72 h .

Antitrypanosomal agent 13	Parasite	Infection
Antitrypanosomal agent 13 (compound 4b) is a potent antitrypanosomal agent. Antitrypanosomal agent 13 has trypanocidal and cytotoxic activity with GI₅₀ values of 0.18 and 8.4 μM for T. brucei and HL-60, respectively .

Monaspin B	Apoptosis	Cancer
Monaspin B is a natural product produced by the co-culture of Monascus purpureus and Aspergillus oryzae. Monaspin B exerts anti-proliferation activity by inducing apoptosis of HL-60 cells, IC₅₀ 160 nM. Monaspin B has antitumor activity .

FD274	PI3K mTOR	Cancer
FD274 is a highly potent PI3K/mTOR dual inhibitor with IC₅₀s of 0.65 nM, 1.57 nM, 0.65 nM, 0.42 nM, and 2.03 nM against PI3Kα/β/γ/δ and mTOR, respectively. FD274 exhibits significant anti-proliferation of AML cell lines (HL-60 and MOLM-16). FD274 demonstrates dose-dependent inhibition of tumor growth in the HL-60 xenograft model. FD274 has the potential for acute myeloid leukemia research .

Anticancer agent 196	DNA/RNA Synthesis	Cancer
Anticancer agent 196 (compound 1) shows cell cytotoxicity with IC₅₀ values of 7.69 µM and 54.2 µM for HL-60 cells and A549 cells, respectively. Anticancer agent 196 can induce DNA damage .

O-allylvanillin	Others	Others
O-allylvanillin is O-allylchalcone derivative with anti-cancer effects . O-allylvanillin inhibits THP-1, HL60, Hep-G2, MCF-7 cells growth with IC₅₀ values of 74.76 μM, 63.52 μM, 90.99 μM, and 90.11 μM, respectively .

Theasaponin E1	Others	Cancer
Theasaponin E1 is a tea saponin isolated from tea seeds. Theasaponin E1 exhibits potential antitumor activity against human tumor cell lines K562 and HL60. Theasaponin E1 also has quinone reductase (QR)-inducing activity and can act as an anti-tumor agent for cancer prevention .

Ursonic acid methyl ester	Others	Cancer
Ursonic acid methyl ester is an esterified derivative of Ursolic acid (HY-N0140). Ursonic acid methyl ester shows growth inhibitory activity against four tumor cell lines, HL-60, BGC, Bel-7402 and Hela with ED₅₀ values of >100 µg/ml .

Ajoene	Fungal Apoptosis	Infection Cancer
Ajoene, a garlic-derived compound, is an antithrombotic and antifungal agent. Ajoene inhibits proliferation and induces apoptosis of human leukaemia CD34-negative cells including HL-60, U937, HEL and OCIM-I. Anticancer activities .

Anticancer agent 197	DNA/RNA Synthesis	Cancer
Anticancer agent 197 (compound 2b) shows cell cytotoxicity with IC₅₀ values of 10.03 µM and 73.54 µM for HL-60 cells and A549 cells, respectively. Anticancer agent 197 can induce DNA damage .

Asperphenamate	Autophagy Cathepsin	Infection Inflammation/Immunology Cancer
Asperphenamate, a fungal metabolite of Aspergillus flatiipes with anti-cancer effect, exhibits IC₅₀ values of 92.3 μM, 96.5 μM and 97.9 μM in T47D, MDA-MB-231 and HL-60 cells, respectively .

Cat. No.	Product Name	Type

HY-B1046

Clofazimine

5+ Cited Publications

Chromogenic Assays

Clofazimine is an orally-active anti-mycobacterial agent with a wide range of anti-mycobacterial activity including leprosy and tuberculosis. Clofazimine exerts anti-inflammatory activities and anti-tumor activities by interfering DNA replication and inhibiting IL2 (IC₅₀ = 1.10 ± 0.26 μM, Jurkat T) production. Clofazimine can be used in mycobacterial and cancer research .

Cat. No.	Product Name	Target	Research Area

HY-W588250

Surfactin C1	Integrin	Inflammation/Immunology
Surfactin C1 is an amphiphilic biosurfactants. Surfactin C1 inhibits leukemic cell (HL-60) adhesion to human umbilical vein endothelial cells (HUVEC). Surfactin C1 inhibits adhesion melecules expression, such as ICAM-1 and VCAM-1 .

HY-P3736

Myelopeptide-2 MP-2	Interleukin Related	Cancer
Myelopeptide-2 is a peptide originally isolated from the supernatant of porcine bone marrow cell cultures, can restore mitogenic reactivity of human T lymphocytes inhibited by HL-60 leukemia cells or measles virus conditions. Myelopeptide-2 also recover depressed interleukin-2 (IL-2) synthesis and interleukin-2 receptor (IL-2R) expression. Myelopeptide-2 involves in immunity homeostasis, is perspective to be applied in antitumor and antivirus research .

HY-13589

Cemadotin LU103793 free base	Microtubule/Tubulin	Cancer
Cemadotin (LU103793) is an analogue of Dolastatin 15 (HY-P1126) which is naturally occurring cytotoxic peptides. Cemadotin blocks cells at mitosis, and exhibits K_i value of 1 μM for inhibiting tubulin. Cemadotin can be used to research anticancer .

Species:	Human (3)
Tag:	His (3)
Source:	Sf9 insect cells (1) E. coli (2)

Cat. No.	Compare	Product Name	Species	Source

HY-P70990

	PADI4 Protein, Human (His) Protein-Arginine Deiminase Type-4; HL-60 PAD; Peptidylarginine Deiminase IV; Protein-arginine Deiminase type IV; PADI4; PADI5; PDI5	Human	E. coli
	PADI4 is a hydrolase that converts arginine residues in histones to citrulline. PADI4 promotes tumor progression by up-regulating the cytokine receptor CXCR2. PADI4 can also cause inflammation and immune responses. PADI4 Protein, Human (His) is the recombinant human-derived PADI4 protein, expressed by E. coli , with N-6*His labeled tag. The total length of PADI4 Protein, Human (His) is 663 a.a., with molecular weight of 71-78 kDa.

HY-P701030

	PADI4 Protein, Human (Biotinylated, His) Protein-arginine deiminase type-4; HL-60 PAD; HL60 PAD; HL-60; PAD; PAD4; PADI5; PDI5	Human	E. coli
	The PADI4 protein catalyzes the citrullination of arginine residues in proteins such as histones, contributing to the histone code and stem cell regulation. PADI4 Protein, Human (Biotinylated, His) is the recombinant human-derived PADI4 protein, expressed by E. coli , with N-His labeled tag. The total length of PADI4 Protein, Human (Biotinylated, His) is 663 a.a., with molecular weight of 76.6 kDa.

HY-P77121

	PADI4 Protein, Human (sf9, His) Protein-Arginine Deiminase Type-4; HL-60 PAD; Peptidylarginine Deiminase IV; PADI5; PDI5	Human	Sf9 insect cells
	PADI4 is a hydrolase that converts arginine residues in histones to citrulline. PADI4 promotes tumor progression by up-regulating the cytokine receptor CXCR2. PADI4 can also cause inflammation and immune responses. PADI4 Protein, Human (sf9, His) is the recombinant human-derived PADI4 protein, expressed by Sf9 insect cells , with N-His labeled tag. The total length of PADI4 Protein, Human (sf9, His) is 663 a.a., with molecular weight of ~76.3 KDa.

Cat. No.	Product Name	Chemical Structure

HY-B1490AS

Imipramine-d6

Imipramine-d₆ is the deuterium labeled Imipramine hydrochloride. Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6].

HY-B1490S

Imipramine-d4 hydrochloride

Imipramine-d₄ (hydrochloride) is the deuterium labeled Imipramine hydrochloride. Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. Imipramine hydrochloride is a Fascin1 inhibitor with antitumor activities. Imipramine hydrochloride also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine hydrochloride stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine hydrochloride shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6].

HY-B1490AS1

Imipramine-d4

Imipramine-d₄ is deuterium labeled Imipramine. Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6].

HY-B1490S1

Imipramine-d3 hydrochloride

Imipramine-d₃ (hydrochloride) is deuterium labeled Imipramine (hydrochloride). Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6].

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