Curcumol, 98%

Name: Curcumol, 98% | 4871-97-0
Brand: J&K Chemical
SKU: JK271808_10_MG
Price: 304.0 USD
Availability: OutOfStock

Cat. No JK271808_10_MG

Vendor: J&K Chemical

Product Information

Product Name

Curcumol, 98%

Brand Name

J&K

Product Number

271808

CAS

4871-97-0

Molecular Formula

C15H24O2

Molecular Weight

236.35

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

(3S,3aS,5S,6R,8aS)-Octahydro-3-methyl-8-methylene-5-(1-methylethyl)-6H-3a,6-epoxyazulen-6-ol

PubChem CID

14240392

IUPAC Name

(1S,2S,5S,8R,9S)-2-methyl-6-methylidene-9-propan-2-yl-11-oxatricyclo6.2.1.01,5undecan-8-ol

InChI Key

QRMPRVXWPCLVNI-YYFQZIEXSA-N

SMILES

CC@H1CCC@@H2C@13CC@H(C@(O3)(CC2=C)O)C(C)C

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Design, synthesis and anti-GBM activities of amide-modified Curcumol derivatives

Publication Name: Bioorganic & Medicinal Chemistry Letters

Publication Date: 2025-09-01

DOI: 10.1016/j.bmcl.2025.130265

Enhancing curcumol delivery through PD-1 targeted nanocarriers: A novel therapeutic approach for prostate cancer

Publication Name: Phytomedicine : international journal of phytotherapy and phytopharmacology

Publication Date: 2025-06

DOI: 10.1016/j.phymed.2025.156595

Curcumol Ameliorates Cisplatin-induced Nephrotoxicity by Targeting TAK1 and Inhibiting MAPK and NF-κB Pathways

Publication Name: Phytomedicine : international journal of phytotherapy and phytopharmacology

Publication Date: 2025-06

DOI: 10.1016/j.phymed.2025.156752

Mechanism of Curcumol Targeting the OTUB1/TGFBI Ubiquitination Pathway in the Inhibition of Angiogenesis in Colon Cancer

Publication Name: International Journal of Molecular Sciences

Publication Date: 2025-05-21

DOI: 10.3390/ijms26104899

Curcumol attenuates hyperproliferation and inflammatory response in a psoriatic HaCaT keratinocyte model by inhibiting the PI3K-Akt pathway and ameliorates skin lesions and inflammatory status in psoriasis-like mice

Publication Name: Inflammopharmacology

Publication Date: 2025-03-10

DOI: 10.1007/s10787-025-01708-y

Curcumol, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Design, synthesis and anti-GBM activities of amide-modified Curcumol derivatives

Enhancing curcumol delivery through PD-1 targeted nanocarriers: A novel therapeutic approach for prostate cancer

Curcumol Ameliorates Cisplatin-induced Nephrotoxicity by Targeting TAK1 and Inhibiting MAPK and NF-κB Pathways

Mechanism of Curcumol Targeting the OTUB1/TGFBI Ubiquitination Pathway in the Inhibition of Angiogenesis in Colon Cancer

Curcumol attenuates hyperproliferation and inflammatory response in a psoriatic HaCaT keratinocyte model by inhibiting the PI3K-Akt pathway and ameliorates skin lesions and inflammatory status in psoriasis-like mice

Curcumol, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Curcumol, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Design, synthesis and anti-GBM activities of amide-modified Curcumol derivatives

Enhancing curcumol delivery through PD-1 targeted nanocarriers: A novel therapeutic approach for prostate cancer

Curcumol Ameliorates Cisplatin-induced Nephrotoxicity by Targeting TAK1 and Inhibiting MAPK and NF-κB Pathways

Mechanism of Curcumol Targeting the OTUB1/TGFBI Ubiquitination Pathway in the Inhibition of Angiogenesis in Colon Cancer

Curcumol attenuates hyperproliferation and inflammatory response in a psoriatic HaCaT keratinocyte model by inhibiting the PI3K-Akt pathway and ameliorates skin lesions and inflammatory status in psoriasis-like mice

Curcumol, 98%

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2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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