[(1R,3R,6S,7S,9S,10S,11S,12R,13S,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-4-oxo-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-12-yl] acetate

Details

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Internal ID 5f38a97a-e3cd-4902-9119-4de6ccbf2fc2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Dolabellane and neodolabellane diterpenoids
IUPAC Name [(1R,3R,6S,7S,9S,10S,11S,12R,13S,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-4-oxo-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-12-yl] acetate
SMILES (Canonical) CC1CC23C(CC1=O)(C4(CC(O2)(C5(C3(C4(C(C5(C(C)C)O)OC(=O)C)O)O)C)O)C)O
SMILES (Isomeric) C[C@@H]1C[C@]23[C@](CC1=O)([C@@]4(C[C@](O2)([C@@]5([C@]3([C@]4([C@@H]([C@@]5(C(C)C)O)OC(=O)C)O)O)C)O)C)O
InChI InChI=1S/C22H32O9/c1-10(2)20(27)14(30-12(4)23)21(28)15(5)9-19(26)16(20,6)22(21,29)18(31-19)7-11(3)13(24)8-17(15,18)25/h10-11,14,25-29H,7-9H2,1-6H3/t11-,14-,15+,16+,17+,18-,19+,20-,21-,22+/m1/s1
InChI Key VQIXTEBDQIBFTP-TXJORZTCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H32O9
Molecular Weight 440.50 g/mol
Exact Mass 440.20463259 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP -1.50
Atomic LogP (AlogP) -0.60
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,3R,6S,7S,9S,10S,11S,12R,13S,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-4-oxo-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-12-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8395 83.95%
Caco-2 - 0.7012 70.12%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6379 63.79%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8763 87.63%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7862 78.62%
P-glycoprotein inhibitior - 0.6838 68.38%
P-glycoprotein substrate - 0.5329 53.29%
CYP3A4 substrate + 0.6526 65.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8717 87.17%
CYP3A4 inhibition - 0.6477 64.77%
CYP2C9 inhibition - 0.8703 87.03%
CYP2C19 inhibition - 0.8449 84.49%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.8410 84.10%
CYP2C8 inhibition - 0.8487 84.87%
CYP inhibitory promiscuity - 0.9767 97.67%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6417 64.17%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8935 89.35%
Skin irritation - 0.6396 63.96%
Skin corrosion - 0.9072 90.72%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4487 44.87%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6027 60.27%
skin sensitisation - 0.8661 86.61%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.7164 71.64%
Acute Oral Toxicity (c) I 0.3753 37.53%
Estrogen receptor binding + 0.8409 84.09%
Androgen receptor binding + 0.7521 75.21%
Thyroid receptor binding + 0.6823 68.23%
Glucocorticoid receptor binding + 0.6915 69.15%
Aromatase binding + 0.6104 61.04%
PPAR gamma + 0.6105 61.05%
Honey bee toxicity - 0.7912 79.12%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5450 54.50%
Fish aquatic toxicity + 0.9767 97.67%

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 97.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.07% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.88% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.04% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.78% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.77% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.59% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 86.30% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.24% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 85.22% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.38% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.26% 91.07%
CHEMBL4040 P28482 MAP kinase ERK2 82.66% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.20% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.41% 97.14%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.07% 85.30%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.80% 85.14%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.34% 89.50%

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.
Persea indica

Cross-Links

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PubChem 101093084
NPASS NPC160023
LOTUS LTS0044340
wikiData Q105291290