[(1R,2R,4R,5R,9S,10R,13S,15R)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate

Details

Top
Internal ID dba4a29b-b9eb-49c0-a68f-7ccd5a556423
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1R,2R,4R,5R,9S,10R,13S,15R)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical) CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4O)C)(C)CO
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@H]2[C@](CCC[C@@]2([C@@H]3[C@@]14C[C@H](CC3)C(=C)[C@H]4O)C)(C)CO
InChI InChI=1S/C22H34O4/c1-13-15-6-7-16-21(4)9-5-8-20(3,12-23)17(21)10-18(26-14(2)24)22(16,11-15)19(13)25/h15-19,23,25H,1,5-12H2,2-4H3/t15-,16+,17-,18+,19+,20-,21+,22-/m0/s1
InChI Key MMPSMJLFQSNILL-AABPEDEVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H34O4
Molecular Weight 362.50 g/mol
Exact Mass 362.24570956 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(1R,2R,4R,5R,9S,10R,13S,15R)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9851 98.51%
Caco-2 + 0.6651 66.51%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7549 75.49%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.8500 85.00%
OATP1B3 inhibitior + 0.8143 81.43%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6869 68.69%
BSEP inhibitior + 0.5728 57.28%
P-glycoprotein inhibitior - 0.7547 75.47%
P-glycoprotein substrate - 0.7565 75.65%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.8025 80.25%
CYP2C9 inhibition - 0.7214 72.14%
CYP2C19 inhibition - 0.8388 83.88%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.7471 74.71%
CYP2C8 inhibition - 0.5810 58.10%
CYP inhibitory promiscuity - 0.8195 81.95%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6607 66.07%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.8789 87.89%
Skin irritation + 0.5111 51.11%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7033 70.33%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.6522 65.22%
skin sensitisation - 0.8960 89.60%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4625 46.25%
Acute Oral Toxicity (c) III 0.5338 53.38%
Estrogen receptor binding + 0.8211 82.11%
Androgen receptor binding + 0.6034 60.34%
Thyroid receptor binding + 0.6665 66.65%
Glucocorticoid receptor binding + 0.8035 80.35%
Aromatase binding + 0.6183 61.83%
PPAR gamma + 0.5994 59.94%
Honey bee toxicity - 0.8243 82.43%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9969 99.69%

Targets

Top

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 96.41% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.50% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.24% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.26% 97.25%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 90.16% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.71% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 87.19% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.55% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.53% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.94% 82.69%
CHEMBL237 P41145 Kappa opioid receptor 83.90% 98.10%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.16% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.80% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 82.61% 95.38%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 81.64% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.17% 91.07%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.07% 92.62%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.95% 96.38%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.63% 92.94%

Plants that contains it

Top
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.
Sideritis leptoclada
Sideritis stricta

Cross-Links

Top
PubChem 162996404
LOTUS LTS0153725
wikiData Q105167965