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Natural Product (NP) Details

General Information of the NP (ID: NP3875)
Name
Cryptoxanthin
Synonyms
beta-Cryptoxanthin; Cryptoxanthin; 472-70-8; (3R)-beta,beta-caroten-3-ol; UNII-6ZIB13GI33; 6ZIB13GI33; (1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-3-en-1-ol; Cryptoxanthins; beta,beta-carotene-3-ol; Neo-beta-cryptoxanthin; 3-Hydroxy-beta-carotene; beta-cryptoxanthins; beta,beta-Caroten-3-ol, (3R)-; SCHEMBL24469; CHEBI:10362; DTXSID30912309; ZINC4097702; beta-Cryptoxanthin, >=97% (TLC); LMPR01070269; HY-108059; CS-0027251; C08591; Q392062; 5-AMINOMETHYL-2-HYDROXY-BENZOICACIDMETHYLESTER; UNII-177RP9H0XI component DMASLKHVQRHNES-FKKUPVFPSA-N
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Species Origin Capsicum annum ...     Click to Show/Hide
Capsicum annum
Kingdom: Viridiplantae
Phylum: Streptophyta
Class: Magnoliopsida
Order: Solanales
Family: Solanaceae
Genus: Capsicum
Species: Capsicum annum
Disease Stomach cancer [ICD-11: 2B72] Investigative [1]
Structure
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2D MOL

3D MOL

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Formula
C40H56O
PubChem CID
5281235
Canonical SMILES
CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C
InChI
1S/C40H56O/c1-30(18-13-20-32(3)23-25-37-34(5)22-15-27-39(37,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-38-35(6)28-36(41)29-40(38,9)10/h11-14,16-21,23-26,36,41H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+/t36-/m1/s1
InChIKey
DMASLKHVQRHNES-FKKUPVFPSA-N
CAS Number
CAS 472-70-8
ChEBI ID
CHEBI:10362
Herb ID
HBIN021796
SymMap ID
SMIT00297
TCMSP ID
MOL009674
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally
    α. A List of Drug(s) Whose Efficacy can be Enhanced by This NP
          Cisplatin      Bladder cancer     Click to Show/Hide the Molecular Data of This Drug
                 Achieving Therapeutic Synergy     Click to Show/Hide
                    Representative Experiment Reporting the Effect of This Combination [2]
                    Detail(s)  Combination Info  click to show the detail info of this combination
                    Molecule(s)
                    Regulation
Down-regulation Expression BCL-2  Molecule Info 
Pathway MAP
                    In-vitro Model BGC-823 CVCL_3360 Gastric cancer Homo sapiens
                    Experimental
                    Result(s)
The combination of crocin with cisplatin suppresses growth of gastric carcinoma cell line BGC-823 and promotes cell apoptosis.
Target and Pathway
Target(s) ATP-binding cassette A1 (ABCA1)  Molecule Info  [3]
KEGG Pathway ABC transporters Click to Show/Hide
2 Fat digestion and absorption
NetPath Pathway Leptin Signaling Pathway Click to Show/Hide
Pathway Interaction Database RXR and RAR heterodimerization with other nuclear receptor Click to Show/Hide
Reactome HDL-mediated lipid transport Click to Show/Hide
2 PPARA activates gene expression
WikiPathways Statin Pathway Click to Show/Hide
2 Nuclear Receptors in Lipid Metabolism and Toxicity
3 Regulation of Lipid Metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha)
4 Lipid digestion, mobilization, and transport
5 SREBF and miR33 in cholesterol and lipid homeostasis
6 Folate Metabolism
7 Vitamin B12 Metabolism
8 Selenium Micronutrient Network
References
Reference 1 Beta-Cryptoxanthin induced anti-proliferation and apoptosis by G0/G1 arrest and AMPK signal inactivation in gastric cancer. Eur J Pharmacol. 2019 Sep 15;859:172528.
Reference 2 The combination of crocin with cisplatin suppresses growth of gastric carcinoma cell line BGC-823 and promotes cell apoptosis. Pak J Pharm Sci. 2017 Sep;30(5):1629-1634.
Reference 3 The crosstalk of ABCA1 and ANXA1: a potential mechanism for protection against atherosclerosis. Mol Med. 2020 Sep 7;26(1):84.
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Cite NPCDR
Visitor Map
Correspondence

X. N. Sun, Y. T. Zhang, Y. Zhou, X. C. Lian, L. L. Yan, T. Pan, T. Jin, H. Xie, Z. M. Liang, W. Q. Qiu, J. X. Wang, Z. R. Li, F. Zhu*, X. B. Sui*. NPCDR: natural product-based drug combination and its disease-specific molecular regulation. Nucleic Acids Research. 50(D1): 1324-1333 (2020). PMID: 34664659

Prof. Feng ZHU  (zhufeng@zju.edu.cn)

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China


Prof. Xinbing SUI  (hzzju@hznu.edu.cn)

School of Pharmacy and Department of Medical Oncology, the Affiliated Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou, China