9-Cyclopentyladenine monomethanesulfonate - ≥97% , CAS No.189639-09-6

CAS: 189639-09-6 Cat. No.: C334623 Peso molecular: 299.35
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
9-Cyclopentyladenine monomethanesulfonate | PS-6133 | 2-Carboxylic acid-pyridine-1-oxide | SMR001230763 | HMS3260H08 | NCGC00016126-01 | AS-16985 | DTXSID90424973 | MLS002153371 | J-012234 | 9-CP-Ade | EU-0100273 | PD015328 | 1-(chloromethyl)-4-(methyloxy
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
C334623-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
171,90US$
5mg
C334623-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
432,90US$
10mg
C334623-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
631,90US$
25mg
C334623-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.563,90US$
50mg
C334623-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.465,90US$
100mg
C334623-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.999,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

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

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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.

Descripción general

9-Cyclopentyladenine monomethanesulfonate is a stable, cell-permeable, non-competitive adenylyl cyclase inhibitor that targets the P-site domain. In detergent-dispersed rat brain preparation, 9-Cyclopentyladenine monomethanesulfonate has an IC|50|= 100 μM

Specifications

Sinónimos
9-Cyclopentyladenine monomethanesulfonate | PS-6133 | 2-Carboxylic acid-pyridine-1-oxide | SMR001230763 | HMS3260H08 | NCGC00016126-01 | AS-16985 | DTXSID90424973 | MLS002153371 | J-012234 | 9-CP-Ade | EU-0100273 | PD015328 | 1-(chloromethyl)-4-(methyloxy
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥97%
Nombres e identificadores
Sonrisas canónicasCS(=O)(=O)O.C1CCC(C1)N2C=NC3=C(N=CN=C32)N
IUPAC Name9-cyclopentylpurin-6-amine;methanesulfonic acid
InChIKeyAJMDRSJHCYQPQI-UHFFFAOYSA-N
INCHI1S/C10H13N5.CH4O3S/c11-9-8-10(13-5-12-9)15(6-14-8)7-3-1-2-4-7;1-5(2,3)4/h5-7H,1-4H2,(H2,11,12,13);1H3,(H,2,3,4)
Isómeros SMILES CS(=O)(=O)O.C1CCC(C1)N2C=NC3=C(N=CN=C32)N
WGK Alemania 3
Peso molecular 299.35
Reaxy-Rn 32366842
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=32366842&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
SuperclassOrganoheterocyclic compounds
ClaseImidazopyrimidines
SubclassPurines and purine derivatives
Intermediate Tree Nodes Not available
Direct Parent6-aminopurines
Alternative Parents Aminopyrimidines and derivatives  N-substituted imidazoles  Imidolactams  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkNot available
Substituents 6-aminopurine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Azacycle - Organonitrogen compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Primary amine - Organopnictogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CYP3A4 Tclin Cytochrome P450 3A4 (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
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 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
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THPO Tbio Thrombopoietin (834 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadSoluble in minimum of 100 mg/mL water
SensibilidadMoisture sensitive
Punto de fusión (°C)180-183° C
Peso molecular299.350 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count1
Exact Mass299.105 Da
Monoisotopic Mass299.105 Da
Topological Polar Surface Area132.000 Ų
Heavy Atom Count20
Formal Charge0
Complexity320.000
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 Count2
Calculadoras de soluciones
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