(4R,6S,10R,12S,13S,17S,18R)-10,18-dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde

Details

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Internal ID d36c2e79-d522-4e93-8863-a9f8ec00741b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (4R,6S,10R,12S,13S,17S,18R)-10,18-dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde
SMILES (Canonical) CC1(CCCC23C1CC(C45C2C(CC(C4O)C(=C)C5=O)(OC3)OC)O)C=O
SMILES (Isomeric) C[C@@]1(CCCC23[C@@H]1C[C@H](C45[C@H]2[C@@](C[C@H]([C@H]4O)C(=C)C5=O)(OC3)OC)O)C=O
InChI InChI=1S/C21H28O6/c1-11-12-8-20(26-3)17-19(10-27-20)6-4-5-18(2,9-22)13(19)7-14(23)21(17,15(11)24)16(12)25/h9,12-14,16-17,23,25H,1,4-8,10H2,2-3H3/t12-,13+,14+,16+,17+,18+,19?,20+,21?/m0/s1
InChI Key WGCKEVDKYAWWFQ-MGNJTJOSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O6
Molecular Weight 376.40 g/mol
Exact Mass 376.18858861 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.20
Atomic LogP (AlogP) 1.24
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,6S,10R,12S,13S,17S,18R)-10,18-dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9704 97.04%
Caco-2 + 0.5057 50.57%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7276 72.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8664 86.64%
OATP1B3 inhibitior + 0.9560 95.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7309 73.09%
BSEP inhibitior - 0.5548 55.48%
P-glycoprotein inhibitior - 0.7947 79.47%
P-glycoprotein substrate - 0.5444 54.44%
CYP3A4 substrate + 0.6625 66.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8302 83.02%
CYP3A4 inhibition - 0.7544 75.44%
CYP2C9 inhibition - 0.7761 77.61%
CYP2C19 inhibition - 0.8789 87.89%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.7870 78.70%
CYP2C8 inhibition + 0.5137 51.37%
CYP inhibitory promiscuity - 0.9078 90.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6282 62.82%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9472 94.72%
Skin irritation - 0.5897 58.97%
Skin corrosion - 0.9277 92.77%
Ames mutagenesis - 0.6519 65.19%
Human Ether-a-go-go-Related Gene inhibition - 0.4061 40.61%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5926 59.26%
skin sensitisation - 0.8700 87.00%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.7046 70.46%
Acute Oral Toxicity (c) I 0.2897 28.97%
Estrogen receptor binding + 0.8847 88.47%
Androgen receptor binding + 0.6495 64.95%
Thyroid receptor binding + 0.6446 64.46%
Glucocorticoid receptor binding + 0.7750 77.50%
Aromatase binding + 0.5666 56.66%
PPAR gamma + 0.5753 57.53%
Honey bee toxicity - 0.6463 64.63%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9925 99.25%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.28% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.47% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.37% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.23% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.55% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.15% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.91% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.88% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.60% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.76% 97.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.10% 96.09%
CHEMBL1902 P62942 FK506-binding protein 1A 83.92% 97.05%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.68% 93.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.39% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.18% 85.14%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.85% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.74% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.36% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.33% 96.77%
CHEMBL340 P08684 Cytochrome P450 3A4 80.89% 91.19%

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.
Isodon macrocalyx

Cross-Links

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PubChem 101920416
LOTUS LTS0151705
wikiData Q105304352