Protosappanin A - ≥99% , CAS No.102036-28-2

CAS: 102036-28-2 Cat. No.: P646214 Peso molecular: 272.25 PubChem CID: 128001
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
HY-113573 | CHEBI:69202 | MS-23852 | Q27137541 | 6H-Dibenz(b,d)oxocin-7(8H)-one, 3,10,11-trihydroxy- | 3,10,11-trihydroxy-7,8-dihydro-6h-dibenz[b,d]oxocin-7-one | AKOS040760044 | Protosappanin A | 5,14,15-trihydroxy-8-oxatricyclo[10.4.0.02,7]hexadeca-1(16
Storage
Store at 2-8°C,Protected from light,Desiccated
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
P646214-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

77,90US$

116,90US$
Guardar 39,00 US$ (33.36%)
5mg
P646214-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

100,90US$

151,90US$
Guardar 51,00 US$ (33.57%)
10mg
P646214-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

130,90US$

196,90US$
Guardar 66,00 US$ (33.52%)
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Desiccated Ships Wet ice 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.

Descripción general

Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3 -dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3

In Vitro

Protosappanin A (PTA: 12.5, 25, 50 μM, 24 hours) significantly inhibits the production of TNF-α and IL-1β in LPS-activated BV2 microglia. And the mRNA expressions of IL-6, IL-1β, and MCP-1 are reduced by PTA in a dose-dependent manner in BV2 microglial cell line. Protosappanin A (PTA: 12.5, 25, 50 μM, 24 hours) suppresses JAK2/STAT3-dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3, as well as STAT3 nuclear translocation against LPS treatment. Protosappanin A (PTA: 12.5, 25, 50 μM, 24 hours) shows obvious effect on disturbing the interaction of transmembrane protein CD14 with Toll-like receptor-4, resulting in the inhibition of NF-κB-dependent oxidative and nitrative stress in LPS-induced BV2 microglia. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: Murine BV2 microglial cell line. Concentration: 12.5, 25, 50 μM. Incubation Time: 24 hours. Result: Inhibits the releases of NO, TNF-α and IL-1β in LPS-induced BV2 cells. Attenuated IL-6, IL-1β and MCP-1 gene expressions in the LPS-induced BV2 cells. Suppressed JAK2/STAT3 pathway activation in the LPS-induced BV2 cells.

Form:Solid

IC50& Target:JAK2 STAT3

Specifications

Sinónimos
HY-113573 | CHEBI:69202 | MS-23852 | Q27137541 | 6H-Dibenz(b, d)oxocin-7(8H)-one, 3, 10, 11-trihydroxy- | 3, 10, 11-trihydroxy-7, 8-dihydro-6h-dibenz[b, d]oxocin-7-one | AKOS040760044 | Protosappanin A | 5, 14, 15-trihydroxy-8-oxatricyclo[10.4.0.02, 7]hexadeca-1(16
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3 -dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Desiccated
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥99%
Nombres e identificadores
Sonrisas canónicasC1C(=O)COC2=C(C=CC(=C2)O)C3=CC(=C(C=C31)O)O
IUPAC Name5,14,15-trihydroxy-8-oxatricyclo[10.4.0.02,7]hexadeca-1(16),2(7),3,5,12,14-hexaen-10-one
InChIKeyMUKYVRVYBBYJSI-UHFFFAOYSA-N
INCHI1S/C15H12O5/c16-9-1-2-11-12-6-14(19)13(18)4-8(12)3-10(17)7-20-15(11)5-9/h1-2,4-6,16,18-19H,3,7H2
Isómeros SMILES C1C(=O)COC2=C(C=CC(=C2)O)C3=CC(=C(C=C31)O)O
CAS alternativo 102036-28-2
PubChem CID 128001
Términos de entrada MeSH protosappanin A;sappanol B
Peso molecular 272.25

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
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassEthers
Intermediate Tree Nodes Not available
Direct ParentAlkyl aryl ethers
Alternative Parents 1-hydroxy-2-unsubstituted benzenoids  Cyclic ketones  Polyols  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Benzenoid - Cyclic ketone - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group.
External Descriptors catechols
Estructura 3D
Modelo de Estructura Química Interactiva





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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:
Propiedades químicas y físicas
SolubilidadDMSO : 250 mg/mL (918.27 mM; Need ultrasonic)
Peso molecular272.250 g/mol
XLogP32.000
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass272.068 Da
Monoisotopic Mass272.068 Da
Topological Polar Surface Area87.000 Ų
Heavy Atom Count20
Formal Charge0
Complexity371.000
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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