IPAG (1-(4-iodophenyl)-3-(2-adamantyl)guanidine) - ≥98% , CAS No.193527-91-2

CAS: 193527-91-2 Cat. No.: I275981 Peso molecular: 395.29 Número EC: 694-414-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
MS-26649 | SCHEMBL678775 | 1-(4-IODOPHENYL)-3-(2-ADAMANTYL)GUANIDINE | AKOS024458556 | HMS3266K08 | NCGC00024642-01 | BDBM50400914 | NCGC00024642-02 | SR-01000597698 | NSC788127 | NSC-788127 | HY-100985 | HMS3411C22 | IPAG | 1-(Adamantan-2-yl)-3-(4-iodoph
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
I275981-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
72,90US$
5mg
I275981-5mg
3
259,90US$
10mg
I275981-10mg
2
387,90US$
25mg
I275981-25mg
1
783,90US$
50mg
I275981-50mg
1
1.259,90US$
100mg
I275981-100mg
1
1.999,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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.

Specifications

Sinónimos
MS-26649 | SCHEMBL678775 | 1-(4-IODOPHENYL)-3-(2-ADAMANTYL)GUANIDINE | AKOS024458556 | HMS3266K08 | NCGC00024642-01 | BDBM50400914 | NCGC00024642-02 | SR-01000597698 | NSC788127 | NSC-788127 | HY-100985 | HMS3411C22 | IPAG | 1-(Adamantan-2-yl)-3-(4-iodoph
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Selective σ1 antagonist (K i = 8 μM). Shows GTP- and suramin-sensitive affinity binding. Induces cell death and inhibits tumor growth. Active in vitro and in vivo .
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
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.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488194780
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488194780
Sonrisas canónicasC1C2CC3CC1CC(C2)C3N=C(N)NC4=CC=C(C=C4)I
IUPAC Name2-(2-adamantyl)-1-(4-iodophenyl)guanidine
InChIKeyUUKPIWYXWLJPJF-UHFFFAOYSA-N
INCHI1S/C17H22IN3/c18-14-1-3-15(4-2-14)20-17(19)21-16-12-6-10-5-11(8-12)9-13(16)7-10/h1-4,10-13,16H,5-9H2,(H3,19,20,21)
Isómeros SMILES C1C2CC3CC1CC(C2)C3N=C(N)NC4=CC=C(C=C4)I
Peso molecular 395.29
Reaxy-Rn 39949929
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=39949929&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
ClaseBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Not available
Direct ParentIodobenzenes
Alternative Parents Aryl iodides  Guanidines  Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Organopnictogen compounds  Organoiodides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Iodobenzene - Aryl iodide - Aryl halide - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organoiodide - Organohalogen compound - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as iodobenzenes. These are aromatic compounds containing one or more iodine atoms attached to a benzene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CYP2D6 Tclin Cytochrome P450 2D6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CXCR3 Tchem C-X-C chemokine receptor type 3 (2736 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Caco-2 (12174 Activities)
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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSPA5 Tchem 78 kDa glucose-regulated protein (3319 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

11 results found

Lot NumberCertificate TypeFechaArticulo
C2620162Certificate of AnalysisApr 01, 2026 I275981
D2313162Certificate of AnalysisOct 09, 2024 I275981
D2313160Certificate of AnalysisOct 09, 2024 I275981
D2313158Certificate of AnalysisOct 09, 2024 I275981
D2313157Certificate of AnalysisOct 09, 2024 I275981
D2313155Certificate of AnalysisOct 09, 2024 I275981
D2313144Certificate of AnalysisOct 09, 2024 I275981
D2313154Certificate of AnalysisOct 09, 2024 I275981
D2313156Certificate of AnalysisOct 09, 2024 I275981
D2313159Certificate of AnalysisOct 09, 2024 I275981
D2313161Certificate of AnalysisOct 09, 2024 I275981

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Propiedades químicas y físicas
SolubilidadSoluble in ethanol to 10 mM and in DMSO to 100 mM
Peso molecular395.280 g/mol
XLogP33.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count3
Exact Mass395.086 Da
Monoisotopic Mass395.086 Da
Topological Polar Surface Area50.400 Ų
Heavy Atom Count21
Formal Charge0
Complexity386.000
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
Calculadoras de soluciones
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