T0070907 - Moligand™, ≥99% , Antagonist of Peroxisome proliferator-activated receptor-γ, CAS No.313516-66-4, Antagonist of Peroxisome proliferator-activated receptor-γ

CAS: 313516-66-4 Cat. No.: T125937 Molecular Weight: 277.66 EC Number: 631-142-7 PubChem CID: 2777391
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%
Synonyms
N2LK5944GW | Oprea1_586106 | SR-01000392700 | T0070907 | T-0070907 | CHEBI:92553 | EN300-7415023 | FRPJSHKMZHWJBE-UHFFFAOYSA-N | HMS3651P21 | SR-01000392700-1 | HMS3677C22 | HY-13202 | s10640 | 2-CHLORANYL-5-NITRO-N-PYRIDIN-4-YL-BENZAMIDE | SR-01000392700
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
T125937-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$9.90

$14.90
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25mg
T125937-25mg
1

$12.90

$19.90
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50mg
T125937-50mg
1

$22.90

$34.90
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250mg
T125937-250mg
2

$85.90

$128.90
Save $43.00 (33.36%)
1g
T125937-1g
2

$274.90

$412.90
Save $138.00 (33.42%)
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Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

T0070907 has been used to reduce peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in lipopolysaccharide (LPS)-induced leukemia RAW264.7 cell line.It also has been used to evaluate the involvement of wogonin in alleviating EtOH (ethanol)-induced inflammation in RAW264.7 cell line.

T0070907 or Benzamide has been used as a ADP-ribosyltransferase (ADPRT) inhibitor in rat hippocampal slices. It has also been used for urine analysis in patients diagnosed with acute uncomplicated urinary tract infection.

T0070907 has antimicrotubule, antitumor and radiosensitizing properties. It decreases tubulin protein levels, which is associated with cell cycle arrest, apoptosis and also reduces metastasis of colorectal carcinoma cells. T0070907 is used as a therapeutic target in breast cancer. It stimulates proteasome-dependent degradation of tubulin.

Specifications

Synonyms
N2LK5944GW | Oprea1_586106 | SR-01000392700 | T0070907 | T-0070907 | CHEBI:92553 | EN300-7415023 | FRPJSHKMZHWJBE-UHFFFAOYSA-N | HMS3651P21 | SR-01000392700-1 | HMS3677C22 | HY-13202 | s10640 | 2-CHLORANYL-5-NITRO-N-PYRIDIN-4-YL-BENZAMIDE | SR-01000392700
Specifications & Purity
Moligand™, ≥99%
Biochemical and Physiological Mechanisms
T0070907 is a potent and selective PPARγ antagonist (IC50 = 1 nM). T0070907 displays > 800-fold selectivity for PPARγ over PPARα and PPARδ. Blocks transcriptional activity of PPARγ in vitro and inhibits rosiglitazone-induced adi
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
ANTAGONIST
Mechanism of action
Antagonist of Peroxisome proliferator-activated receptor-γ
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥99%
Names and Identifiers
Pubchem Sid504761974
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504761974
Canonical SmilesC1=CC(=C(C=C1[N+](=O)[O-])C(=O)NC2=CC=NC=C2)Cl
IUPAC Name2-chloro-5-nitro-N-pyridin-4-ylbenzamide
InChIKeyFRPJSHKMZHWJBE-UHFFFAOYSA-N
INCHI1S/C12H8ClN3O3/c13-11-2-1-9(16(18)19)7-10(11)12(17)15-8-3-5-14-6-4-8/h1-7H,(H,14,15,17)
Isomeric SMILES C1=CC(=C(C=C1[N+](=O)[O-])C(=O)NC2=CC=NC=C2)Cl
WGK Germany 3
PubChem CID 2777391
Molecular Weight 277.66

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Halobenzoic acids and derivatives
Direct Parent2-halobenzoic acids and derivatives
Alternative Parents Benzamides  Nitrobenzenes  Benzoyl derivatives  Nitroaromatic compounds  Chlorobenzenes  Pyridines and derivatives  Aryl chlorides  Vinylogous halides  Heteroaromatic compounds  Secondary carboxylic acid amides  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organic oxoazanium compounds  Hydrocarbon derivatives  Organochlorides  Organonitrogen compounds  Organooxygen compounds  Organic zwitterions  Organopnictogen compounds  Organic oxides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 2-halobenzoic acid or derivatives - Benzamide - Nitrobenzene - Nitroaromatic compound - Benzoyl - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Pyridine - Heteroaromatic compound - Vinylogous halide - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic oxoazanium - Azacycle - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organochloride - Organic oxide - Organonitrogen compound - Organic zwitterion - Organooxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 2-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 2-position of the benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RT-112 (346 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT1197 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BFTC-905 (116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HuP-T4 (128 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis C virus (23859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
I2007120Certificate of AnalysisJan 29, 2026 T125937
I2007117Certificate of AnalysisJan 29, 2026 T125937
F2220032Certificate of AnalysisJan 19, 2026 T125937
L2130070Certificate of AnalysisJul 15, 2025 T125937
L2130071Certificate of AnalysisJul 15, 2025 T125937
L2130072Certificate of AnalysisJul 15, 2025 T125937
L2130095Certificate of AnalysisJul 15, 2025 T125937
Chemical and Physical Properties
SolubilitySoluble in DMSO at 10mg/ml. Insoluble in water.
Sensitivitylight sensitive
Molecular Weight277.660 g/mol
XLogP32.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass277.025 Da
Monoisotopic Mass277.025 Da
Topological Polar Surface Area87.800 Ų
Heavy Atom Count19
Formal Charge0
Complexity342.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Jinmiao Tian, Lichao Zhang, Xiaoqin La, Xiaxia Fan, Aiping Li, Changxin Wu, Yuxuan An, Shuning Yan, Xiushan Dong, Haitao Wu, Zhuoyu Li.  (2023)  Tumor-secreted GRP78 induces M2 polarization of macrophages by promoting lipid catabolism.  CELLULAR SIGNALLING,      [PMID:37207940] [10.1016/j.cellsig.2023.110719]
2. Meng-Ke Song, Meng-Qi Wang, Yu-Qing Ruan, Can Cui, Wen-Gang Chen, Opeyemi Joshua Olatunji, Yan Li, Jian Zuo.  (2025)  Qing-Luo-Yin Eases T Cells-Mediated Angiogenesis in Adjuvant-Induced Arthritis Rats by Activating PPARγ.  Journal of Inflammation Research,      [PMID:40093952] [10.2147/JIR.S508316]
3. Qing-qing Fang, Yang-jun Gu, Yong Wang, Zheng-cai Wang, Xiao-ying Lin, Kai Guo, Ze-ming Zhuang, Xin-cao Zhong, Li-yun Zhang, Jian Chen, Wei-qiang Tan.  (2025)  The therapeutic potential of Rosiglitazone in modulating scar formation through PPAR-γ pathway.  EUROPEAN JOURNAL OF PHARMACOLOGY,      [PMID:40054722] [10.1016/j.ejphar.2025.177445]
Solution Calculators
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