methyl (1R,4S,5R,9S,10S,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

Details

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Internal ID e7d4f3a6-4f11-46ba-8604-a95ce3e8d381
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name methyl (1R,4S,5R,9S,10S,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate
SMILES (Canonical) CC12CCCC(C1CCC34C2CCC(C3)C(C4=O)(CO)O)(C)C(=O)OC
SMILES (Isomeric) C[C@@]12CCC[C@@]([C@H]1CC[C@]34[C@H]2CC[C@H](C3)[C@](C4=O)(CO)O)(C)C(=O)OC
InChI InChI=1S/C21H32O5/c1-18-8-4-9-19(2,17(24)26-3)14(18)7-10-20-11-13(5-6-15(18)20)21(25,12-22)16(20)23/h13-15,22,25H,4-12H2,1-3H3/t13-,14+,15+,18-,19-,20-,21+/m1/s1
InChI Key YBCSDOGMTZMEND-XPZYIXMRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O5
Molecular Weight 364.50 g/mol
Exact Mass 364.22497412 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 5
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 methyl (1R,4S,5R,9S,10S,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9361 93.61%
Caco-2 + 0.7001 70.01%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8025 80.25%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.9008 90.08%
OATP1B3 inhibitior + 0.8661 86.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8292 82.92%
BSEP inhibitior - 0.5991 59.91%
P-glycoprotein inhibitior - 0.7817 78.17%
P-glycoprotein substrate - 0.6609 66.09%
CYP3A4 substrate + 0.6752 67.52%
CYP2C9 substrate - 0.6029 60.29%
CYP2D6 substrate - 0.8373 83.73%
CYP3A4 inhibition - 0.7383 73.83%
CYP2C9 inhibition - 0.7833 78.33%
CYP2C19 inhibition - 0.8170 81.70%
CYP2D6 inhibition - 0.9704 97.04%
CYP1A2 inhibition - 0.7458 74.58%
CYP2C8 inhibition - 0.8585 85.85%
CYP inhibitory promiscuity - 0.9812 98.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7407 74.07%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9657 96.57%
Skin irritation - 0.5873 58.73%
Skin corrosion - 0.9567 95.67%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6693 66.93%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7321 73.21%
skin sensitisation - 0.9398 93.98%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8874 88.74%
Acute Oral Toxicity (c) III 0.4292 42.92%
Estrogen receptor binding + 0.8649 86.49%
Androgen receptor binding + 0.5849 58.49%
Thyroid receptor binding + 0.6918 69.18%
Glucocorticoid receptor binding + 0.7982 79.82%
Aromatase binding + 0.7023 70.23%
PPAR gamma - 0.5623 56.23%
Honey bee toxicity - 0.8546 85.46%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9513 95.13%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.35% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.77% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.66% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.02% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 88.47% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.63% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.49% 82.69%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.95% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.72% 95.89%
CHEMBL2581 P07339 Cathepsin D 83.98% 98.95%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.93% 91.24%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.76% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.48% 96.77%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.96% 94.33%
CHEMBL340 P08684 Cytochrome P450 3A4 82.10% 91.19%
CHEMBL1075317 P61964 WD repeat-containing protein 5 81.33% 96.33%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.48% 95.50%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 80.23% 88.81%
CHEMBL1937 Q92769 Histone deacetylase 2 80.09% 94.75%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.06% 97.50%

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.
Parinari sprucei

Cross-Links

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PubChem 163030061
LOTUS LTS0121672
wikiData Q105345765