(1R,2R,6S,7S,8S)-1,5-dimethyl-8-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]tricyclo[4.4.0.02,7]dec-4-en-3-one

Details

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Internal ID 6d82293a-e2ca-4542-9423-18fc25a96d2d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,6S,7S,8S)-1,5-dimethyl-8-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]tricyclo[4.4.0.02,7]dec-4-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H32O7/c1-9-7-11(23)15-13-10(5-6-21(15,4)14(9)13)20(2,3)28-19-18(26)17(25)16(24)12(8-22)27-19/h7,10,12-19,22,24-26H,5-6,8H2,1-4H3/t10-,12+,13+,14+,15+,16+,17-,18+,19-,21+/m0/s1
InChI Key NGDDYINPHJUBKI-IXYIOFDISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O7
Molecular Weight 396.50 g/mol
Exact Mass 396.21480336 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,6S,7S,8S)-1,5-dimethyl-8-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]tricyclo[4.4.0.02,7]dec-4-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7986 79.86%
Caco-2 - 0.7925 79.25%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8023 80.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8380 83.80%
OATP1B3 inhibitior + 0.7887 78.87%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.7276 72.76%
BSEP inhibitior - 0.8475 84.75%
P-glycoprotein inhibitior - 0.7369 73.69%
P-glycoprotein substrate - 0.8836 88.36%
CYP3A4 substrate + 0.6844 68.44%
CYP2C9 substrate - 0.7956 79.56%
CYP2D6 substrate - 0.8844 88.44%
CYP3A4 inhibition - 0.8396 83.96%
CYP2C9 inhibition - 0.7347 73.47%
CYP2C19 inhibition - 0.8210 82.10%
CYP2D6 inhibition - 0.9101 91.01%
CYP1A2 inhibition - 0.6859 68.59%
CYP2C8 inhibition - 0.7327 73.27%
CYP inhibitory promiscuity - 0.8242 82.42%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6621 66.21%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9757 97.57%
Skin irritation - 0.6504 65.04%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.7854 78.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5143 51.43%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5081 50.81%
skin sensitisation - 0.8518 85.18%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7933 79.33%
Acute Oral Toxicity (c) III 0.7548 75.48%
Estrogen receptor binding + 0.7147 71.47%
Androgen receptor binding + 0.6610 66.10%
Thyroid receptor binding + 0.6687 66.87%
Glucocorticoid receptor binding - 0.5124 51.24%
Aromatase binding + 0.5781 57.81%
PPAR gamma + 0.5276 52.76%
Honey bee toxicity - 0.8470 84.70%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8763 87.63%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.21% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.66% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.53% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.66% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 89.55% 93.04%
CHEMBL220 P22303 Acetylcholinesterase 89.52% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.29% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.28% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.13% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.62% 95.89%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.11% 90.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.03% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.81% 89.00%
CHEMBL5255 O00206 Toll-like receptor 4 84.44% 92.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.05% 94.00%
CHEMBL1871 P10275 Androgen Receptor 81.65% 96.43%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.01% 96.90%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.80% 97.36%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.44% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.34% 97.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Tinospora cordifolia

Cross-Links

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PubChem 163105183
LOTUS LTS0037213
wikiData Q105178840