tanshinone VI: isolated from the root of Salvia miltiorrhiza; structure in first source
Flora | Rank | Flora Definition | Family | Family Definition |
---|---|---|---|---|
Salvia | genus | A genus in the mint family (LAMIACEAE).[MeSH] | Lamiaceae | The mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).[MeSH] |
ID Source | ID |
---|---|
PubMed CID | 149138 |
CHEMBL ID | 390741 |
SCHEMBL ID | 14417698 |
MeSH ID | M0240363 |
Synonym |
---|
sodium tanshinone vi 1-phenolate |
CHEMBL390741 |
danshenxinkun a |
1-hydroxy-2-(1-hydroxypropan-2-yl)-8-methylphenanthrene-3,4-dione |
tanshinone vi |
3,4-phenanthrenedione, 1-hydroxy-2-(2-hydroxy-1-methylethyl)-8-methyl- |
121064-74-2 |
i91bp9h8pf , |
65907-75-7 |
unii-i91bp9h8pf |
1,4-phenanthrenedione, 3-hydroxy-2-(2-hydroxy-1-methylethyl)-8-methyl- |
SCHEMBL14417698 |
AC-34178 |
bdbm50476406 |
DTXSID20923661 |
AKOS032949036 |
3-hydroxy-2-(1-hydroxypropan-2-yl)-8-methylphenanthrene-1,4-dione |
MS-24242 |
231292-03-8 |
XD176696 |
CS-0024046 |
HY-N3680 |
AKOS040760361 |
1-hydroxy-2-(1-hydroxypropan-2-yl)-8-methyl-3,4-dihydrophenanthrene-3,4-dione |
Tanshinone VI is an abietane diterpene extracted from the root of Salvia miltiorrhiza Bunge. It is a Chinese traditional crude drug, "Tan-Shen"
Excerpt | Reference | Relevance |
---|---|---|
"Tanshinone VI is an abietane diterpene extracted from the root of Salvia miltiorrhiza Bunge (Labiatae), a Chinese traditional crude drug, "Tan-Shen"." | ( Inhibition of bone resorption by Tanshinone VI isolated from Salvia miltiorrhiza Bunge. Dal Piaz, F; De Tommasi, N; Narducci, P; Nicolin, V; Nori, SL, 2010) | 1.36 |
Excerpt | Relevance | Reference |
---|---|---|
" The lack of toxic effects at the dosage used makes Tanshinone VI a good candidate for its therapeutic use in humans." | ( Tanshinone VI inhibits the expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1. Bossi, F; Nicolin, V; Nori, SL; Valentini, R; Viggiano, A, ) | 1.82 |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Hypoxia-inducible factor 1-alpha | Homo sapiens (human) | IC50 (µMol) | 20.0000 | 0.0007 | 2.4652 | 9.2100 | AID291914; AID291915 |
Endothelial PAS domain-containing protein 1 | Homo sapiens (human) | IC50 (µMol) | 20.0000 | 0.0030 | 2.6002 | 8.5100 | AID291914; AID291915 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID291916 | Viability of human AGS cells under normoxic conditions after 24 hrs by MTT assay | 2007 | Journal of natural products, Jul, Volume: 70, Issue:7 | Abietane diterpenes from Salvia miltiorrhiza inhibit the activation of hypoxia-inducible factor-1. |
AID291918 | Viability of human Hep3B cells under normoxic conditions after 24 hrs by MTT assay | 2007 | Journal of natural products, Jul, Volume: 70, Issue:7 | Abietane diterpenes from Salvia miltiorrhiza inhibit the activation of hypoxia-inducible factor-1. |
AID291915 | Inhibition of HIF1 activation in human Hep3B cells assessed as inhibition of hypoxia-induced luciferase expression after 16 hrs by reporter assay | 2007 | Journal of natural products, Jul, Volume: 70, Issue:7 | Abietane diterpenes from Salvia miltiorrhiza inhibit the activation of hypoxia-inducible factor-1. |
AID291914 | Inhibition of HIF1 activation in human AGS cells assessed as inhibition of hypoxia-induced luciferase expression after 16 hrs by reporter assay | 2007 | Journal of natural products, Jul, Volume: 70, Issue:7 | Abietane diterpenes from Salvia miltiorrhiza inhibit the activation of hypoxia-inducible factor-1. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.86) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (14.29%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (85.71%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |