CDC25 Phosphatase Inhibitor I, BN82002 - ≥97% , CAS No.396073-89-5

CAS: 396073-89-5 Cat. No.: C336618 Molecular Weight: 359.4
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
BCP29552 | GOKYHQGRIIXMNE-UHFFFAOYSA-N | AKOS037515620 | BN82002 | BN-82002 | HSCI1_000079 | HY-112776 | 4-(dimethylamino)-2-methoxy-6-[[methyl-[2-(4-nitrophenyl)ethyl]amino]methyl]phenol | NCGC00165741-01 | BN82002 HYDROCHLORIDE SALT | D93454 | Q27253727
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
C336618-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$186.90
10mg
C336618-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$254.90
25mg
C336618-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$438.90
50mg
C336618-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$786.90
100mg
C336618-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$1,316.90
250mg
C336618-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$2,632.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C 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.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

CDC25 Phosphatase Inhibitor I, BN82002, is a cell-permeable ortho-hydroxybenzylamino compound that has been reported to display antitumor properties. It has been shown to act as a potent, selective and irreversible inhibitor of the CDC25 phosphatase family (IC|50|= 2.4, 3.9, 6.3, 5.4, and 4.6 μM for 25A, 25B2, 25B3, 25C, and 25C-cat, respectively). Reported to display a ~20-fold greater selectivity for CDC25 phosphatases over CD45 tyrosine phosphatase. Also shown to delay cell cycle progression|in vitro|(IC|50|= ~7.2-32.6 μM), and reduces tumor growth in athymic mice xenografted with the human pancreatic cells MIA PaCa-2 (15 mg/kg, i.p. route).

Specifications

Synonyms
BCP29552 | GOKYHQGRIIXMNE-UHFFFAOYSA-N | AKOS037515620 | BN82002 | BN-82002 | HSCI1_000079 | HY-112776 | 4-(dimethylamino)-2-methoxy-6-[[methyl-[2-(4-nitrophenyl)ethyl]amino]methyl]phenol | NCGC00165741-01 | BN82002 HYDROCHLORIDE SALT | D93454 | Q27253727
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
BN82002 is a potent, selective and irreversible pan-inhibitor of the CDC25 phosphatase family. BN82002 inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A and 25C-cat with IC50 values ​​of 2.4, 3.9, 6.3, 5.4 and 4.6 µM, respectively. BN82002 shows approximat
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Purity
≥97%
Names and Identifiers
Canonical SmilesCN(C)C1=CC(=C(C(=C1)OC)O)CN(C)CCC2=CC=C(C=C2)[N+](=O)[O-]
IUPAC Name4-(dimethylamino)-2-methoxy-6-[[methyl-[2-(4-nitrophenyl)ethyl]amino]methyl]phenol
InChIKeyGOKYHQGRIIXMNE-UHFFFAOYSA-N
INCHI1S/C19H25N3O4/c1-20(2)17-11-15(19(23)18(12-17)26-4)13-21(3)10-9-14-5-7-16(8-6-14)22(24)25/h5-8,11-12,23H,9-10,13H2,1-4H3
Isomeric SMILES CN(C)C1=CC(=C(C(=C1)OC)O)CN(C)CCC2=CC=C(C=C2)[N+](=O)[O-]
Molecular Weight 359.4
Reaxy-Rn 9867043
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9867043&ln=

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
ClassPhenols
SubclassMethoxyphenols
Intermediate Tree Nodes Not available
Direct ParentMethoxyphenols
Alternative Parents Aminophenyl ethers  Methoxyanilines  Nitrobenzenes  Phenethylamines  p-Aminophenols  Phenylmethylamines  Benzylamines  Dialkylarylamines  Methoxybenzenes  Nitroaromatic compounds  Anisoles  Phenoxy compounds  Aralkylamines  Alkyl aryl ethers  Trialkylamines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Hydrocarbon derivatives  Organic oxides  Organic salts  Organic zwitterions  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Methoxyphenol - Phenethylamine - Nitrobenzene - Aminophenyl ether - Methoxyaniline - Tertiary aliphatic/aromatic amine - Phenylmethylamine - Phenol ether - Aminophenol - Anisole - Benzylamine - Methoxybenzene - Nitroaromatic compound - Aniline or substituted anilines - Dialkylarylamine - P-aminophenol - Phenoxy compound - Aralkylamine - Alkyl aryl ether - Monocyclic benzene moiety - Organic nitro compound - C-nitro compound - Tertiary aliphatic amine - Tertiary amine - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Ether - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Amine - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organic zwitterion - Organic oxygen compound - Organic oxide - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDC25A Tchem Dual specificity phosphatase Cdc25A (619 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDC25C Tchem Dual specificity phosphatase Cdc25C (295 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
GCN5 Histone acetyltransferase GCN5 (89 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
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 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:
Chemical and Physical Properties
SolubilityDMSO and ethanol
Sensitivitylight sensitive
Melt Point(°C)86-88° C
Molecular Weight359.400 g/mol
XLogP33.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass359.185 Da
Monoisotopic Mass359.185 Da
Topological Polar Surface Area81.800 Ų
Heavy Atom Count26
Formal Charge0
Complexity435.000
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
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.