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  1. General Info
  2. Source Info
  3. Effects Info
  4. Reference
Phytochemical Details
01. General Information
Name Aloin
PubChem CID 12305761
Molecular Weight 418.4g/mol
Synonyms

barbaloin, barbaloin, (S)-isomer, barbaloin, beta-D-isomer, barbaloin, monoglucoside, isobarbaloin

Formula C₂₁H₂₂O₉
SMILES C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)CO)O)O)O)C=C(C=C3O)CO
InChI 1S/C21H22O9/c22-6-8-4-10-14(21-20(29)19(28)17(26)13(7-23)30-21)9-2-1-3-11(24)15(9)18(27)16(10)12(25)5-8/h1-5,13-14,17,19-26,28-29H,6-7H2/t13-,14+,17-,19+,20-,21+/m1/s1
InChIKey AFHJQYHRLPMKHU-OSYMLPPYSA-N
CAS Number 1415-73-2
ChEMBL ID CHEMBL2103763
ChEBI ID CHEBI:2991
Herb ID HBIN015313
KEGG ID C10305
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Source Information of Phytochemical
(1) Aloe barbadensis Cold
Chineses Pinyin LuHui
Use Part Solid Residue Obtained By Evaporating Liquid Which Drains From Leaves
Habitat Egypt , South Africa , Kenya, Nigeria , India
Flavor Bitter
Meridian Tropism Liver, Stomach, Large intestine
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Asparagales
    -->Family: Asphodelaceae
     -->Genus: Aloe
      -->Species: Aloe barbadensis
(2) Aloe barbadensis Cold
Chineses Pinyin BanWenLuHui
Use Part Solid Residue Obtained By Evaporating Liquid Which Drains From Leaves
Habitat India , America , Egypt , South Africa , Kenya, Nigeria
Flavor Bitter
Meridian Tropism Large intestine, Stomach, Liver
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Asparagales
    -->Family: Asphodelaceae
     -->Genus: Aloe
      -->Species: Aloe barbadensis
(3) Aloe ferox Unknown
Chineses Pinyin HaoWangJiaoLuHui
Use Part Solid Residue Obtained By Evaporating Liquid Which Drains From Leaves
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Asparagales
    -->Family: Asphodelaceae
     -->Genus: Aloe
      -->Species: Aloe ferox
03. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Drug(s) whose efficacy can be enhanced by this phytochemical
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Combination Pair ID: 314
Pair Name Aloin, Metformin
Partner Name Metformin
Disease Info [ICD-11: 2C12] Hepatocellular carcinoma Investigative
Biological Phenomena Induction-->Autophagy
Gene Regulation Up-regulation Activity AKT1 hsa207
Up-regulation Activity MTOR hsa2475
Up-regulation Activity PIK3CA hsa5290
In Vitro Model Hep-G2 Hepatoblastoma Homo sapiens (Human) CVCL_0027
BEL-7402 Human papillomavirus-related cervical adenocarcinoma Homo sapiens (Human) CVCL_5492
In Vivo Model For xenograft study, mice were inoculated subcutaneously into the right-back with 7.5×10⁶ HepG2 cells in 200 μl PBS and Matrigel (1:1).
Result Our research demonstrated that the concomitant treatment with aloin and MET enhances the antitumor effect by inhibiting the growth and invasion as well as inducing apoptosis and autophagy in HCC through PI3K/AKT/mTOR pathway.
Combination Pair ID: 759
Pair Name Aloin, Cisplatin
Partner Name Cisplatin
Disease Info [ICD-11: 2C30] Melanoma Investigative
Gene Regulation Up-regulation Expression TG2 hsa7052
Up-regulation Expression TYR hsa7299
In Vitro Model B16-F10 Mouse melanoma Mus musculus (Mouse) CVCL_0159
Result The results suggest that aloin possesses antineoplastic and antimetastatic properties, exerted likely through the induction of melanoma cell differentiation.
Combination Pair ID: 761
Pair Name Aloin, Irinotecan
Partner Name Irinotecan
Disease Info [ICD-11: 2B91] Colorectal cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Down-regulation Phosphorylation AKT1 hsa207
Up-regulation Cleavage CASP3 hsa836
Up-regulation Cleavage CASP9 hsa842
Down-regulation Expression IGF1R hsa3480
Down-regulation Phosphorylation MTOR hsa2475
Up-regulation Cleavage PARP1 hsa142
Down-regulation Phosphorylation PIK3CA hsa5290
In Vitro Model LoVo Colon adenocarcinoma Homo sapiens (Human) CVCL_0399
In Vivo Model 4×10⁶ LoVo cells were suspended in serum-free Matrigel medium.Control (DMSO), CPT-11(2 mg/Kg), Aloin (20 mg/Kg), and combination (2 mg/Kg CPT-11 + 20 mg/Kg Aloin). The mice were treated via intratumor injection, every 48 h for four weeks.
Result Our findings suggests that CPT-11 and Aloin are potential combination treatment partners against colorectal cancer. MicroRNA-133b may serve as a co-therapeutic target with IGF1R against colorectal cancer, which might overcome the existing treatment limitations.
Drug(s) whose toxicity can be decreased by this phytochemical
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Combination Pair ID: 760
Pair Name Aloin, Doxorubicin
Partner Name Doxorubicin
Disease Info [ICD-11: 2A00-2F9Z] Solid tumour or cancer Investigative
Biological Phenomena Induction-->Oxidative Stress
Gene Regulation Down-regulation Expression IL19 hsa29949
Down-regulation Expression IL1B hsa3553
Down-regulation Expression IL6 hsa3569
Down-regulation Expression TNF hsa7124
In Vivo Model Male Wistar rats (150-200 g, age 6-8 weeks) were used in this study.
Result Our results highlight the necessity to further investigate the chemopreventive effects of aloin against other chemotherapeutic agents.
04. Reference
No. Title Href
1 Aloin alleviates doxorubicin-induced cardiotoxicity in rats by abrogating oxidative stress and pro-inflammatory cytokinesAloin alleviates doxorubicin-induced cardiotoxicity in rats by abrogating oxidative stress and pro-inflammatory cytokines. Cancer Chemother Pharmacol. 2020 Sep;86(3):419-426. doi: 10.1007/s00280-020-04125-w. Click
2 Combination of aloin and metformin enhances the antitumor effect by inhibiting the growth and invasion and inducing apoptosis and autophagy in hepatocellular carcinoma through PI3K/AKT/mTOR pathway. Cancer Med. 2020 Feb;9(3):1141-1151. doi: 10.1002/cam4.2723. Click
3 Aloin enhances cisplatin antineoplastic activity in B16-F10 melanoma cells by transglutaminase-induced differentiation. Amino Acids. 2013 Jan;44(1):293-300. doi: 10.1007/s00726-011-1166-x. Click
4 Aloin and CPT-11 combination activates miRNA-133b and downregulates IGF1R- PI3K/AKT/mTOR and MEK/ERK pathways to inhibit colorectal cancer progression. Biomed Pharmacother. 2023 Dec 31;169:115911. doi: 10.1016/j.biopha.2023.115911. Click
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