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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 847163-28-4 Chemical Structure| 847163-28-4

Structure of ML351
CAS No.: 847163-28-4

Chemical Structure| 847163-28-4

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ML351 is a novel chemotype and the first reported selective inhibitor of 15-LOX-1 with IC50 value of 200 nM.

Synonyms: CID 664510

4.5 *For Research Use Only !

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Product Details of ML351

CAS No. :847163-28-4
Formula : C15H11N3O
M.W : 249.27
SMILES Code : N#CC1=C(NC)OC(C2=C3C=CC=CC3=CC=C2)=N1
Synonyms :
CID 664510
MDL No. :MFCD04183120
InChI Key :DYXYXTDIFMDJIR-UHFFFAOYSA-N
Pubchem ID :664510

Safety of ML351

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P264-P270-P301+P310+P330-P405-P501
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
mouse islets 10 μmol/L 24 hours ML351 reduced 12-HETE release and improved glucose-stimulated insulin secretion. Diabetes. 2017 Nov;66(11):2875-2887
Keratinocytes in human skin equivalents 10 µM 24 or 48 hours ML351 significantly elevated the secretion of CCL2, CCL5, and CXCL10, indicating its enhancement of keratinocyte inflammatory responses. Cell Death Dis. 2025 Jan 22;16(1):39
NHEK/SVTERT3-5 cells 10 µM 24 hours ML351 significantly reduced many metabolites of arachidonic and linoleic acid, indicating its inhibition of lipoxygenase activity. Cell Death Dis. 2025 Jan 22;16(1):39
Primary spinal microglia 100 ng/ml 8 and 24 hours To assess the effect of KLA treatment on 15-LOX-1 protein expression. KLA treatment significantly upregulated 15-LOX-1 protein expression in microglia. Pain. 2018 Dec;159(12):2620-2629
HEK-293T cells 0.1 nM-10 μM 30 minutes To evaluate the inhibitory effects of ML351 and ML127 on 15-LOX-1 and 12-LOX-p activity. ML351 significantly inhibited the activity of 15-LOX-1 and 12-LOX-p at low nanomolar concentrations, while ML127 preferentially reduced 15-LOX-1 activity. Pain. 2018 Dec;159(12):2620-2629
human lung macrophages 10 μM 24 hours To evaluate the inhibitory effect of ML351 on chemokine release induced by LPS and Th2 cytokines. Results showed that ML351 significantly inhibited LPS-induced release of CCL2 and CCL3, as well as IL-4-induced release of CCL13 and CCL22. Br J Pharmacol. 2015 Sep;172(17):4319-30

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6J mice Streptozotocin (STZ)-induced type 1 diabetes model Intraperitoneal injection 10, 24, 48 mg/kg Once daily, starting 5 days before STZ and ending 5 days after the last STZ dose ML351 (10 and 24 mg/kg) prevented diabetes development, reduced β-cell oxidative stress, and preserved β-cell mass. The 48 mg/kg dose was ineffective. Diabetes. 2017 Nov;66(11):2875-2887
Mice Subarachnoid hemorrhage model Intraperitoneal injection 50 mg/kg Administered 5 minutes after SAH induction, assessed 1 and 3 days later To evaluate the impact of ML351 on brain injury after SAH. Results showed that ML351 reduced neuronal cell death and improved neurological outcomes. Stroke. 2019 Feb;50(2):520-523
C57BL6J mice Transient middle cerebral artery occlusion (MCAO) model Intraperitoneal injection 50 mg/kg Single dose ML351 reduced hemorrhagic transformation (HT) in wild-type mice and similarly reduced HT following tPA treatment Stroke. 2017 Feb;48(2):445-451
Male Holtzman Sprague-Dawley rats TLR4-dependent NSAID-unresponsive hyperalgesia model Intrathecal injection 0.1–10 μg/10 μl Single injection, 30 minutes pretreatment To evaluate the inhibitory effects of ML351 and ML127 on TLR4-mediated hyperalgesia. ML351 significantly attenuated hyperalgesia at all tested doses, while ML127 showed dose-dependent inhibition at high doses. Pain. 2018 Dec;159(12):2620-2629
Mice LepRdb/db mice (type 2 diabetes model) Intraperitoneal injection 100mg/kg 7 consecutive days To evaluate the effect of ML351 on vascular function and diastolic function in diabetic mice, results showed that ML351 improved endothelium-dependent vasodilation and left ventricular diastolic function Life Sci. 2021 Nov 1;284:119925
Male Swiss Albino mice Ischemia/recanalization (I/R) model Intraperitoneal injection 50 mg/kg Single dose at recanalization To investigate the effects of ML351 on ischemia/recanalization-induced neuroinflammation. Results showed that ML351 significantly reduced infarct volume, neurological deficit score, and lipid peroxidation, and suppressed inflammasome (NLRP1 and NLRP3) activation. Front Cell Neurosci. 2023 Sep 26;17:1277268
Mice Alox12 knockout mice Intraperitoneal injection 10 mg/kg body weight 5 days prior to STZ treatment, during treatment, and 5 days post-STZ treatment, daily administration To evaluate the protective effect of ML351 on STZ-induced glucose intolerance, results showed that ML351 treatment significantly improved glucose tolerance in Alox12 knockout mice J Biol Chem. 2019 Apr 19;294(16):6612-6620

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.01mL

0.80mL

0.40mL

20.06mL

4.01mL

2.01mL

40.12mL

8.02mL

4.01mL

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