[1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethyl-3-oxospiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-12-yl] acetate

Details

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Internal ID d1989e16-8eb9-4139-b50a-c8a4618e23f7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethyl-3-oxospiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-12-yl] acetate
SMILES (Canonical) CC(=O)OC1CC2C3(CCC(=O)C(C3CCC2(C4(C1C5(CC4)C6(CCC(O6)(O5)C(C)(C)O)C)C)C)(C)C)C
SMILES (Isomeric) CC(=O)OC1CC2C3(CCC(=O)C(C3CCC2(C4(C1C5(CC4)C6(CCC(O6)(O5)C(C)(C)O)C)C)C)(C)C)C
InChI InChI=1S/C32H50O6/c1-19(33)36-20-18-22-27(6)12-11-23(34)25(2,3)21(27)10-13-28(22,7)29(8)14-16-31(24(20)29)30(9)15-17-32(37-30,38-31)26(4,5)35/h20-22,24,35H,10-18H2,1-9H3
InChI Key ZHCMMSAQQHMOOP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H50O6
Molecular Weight 530.70 g/mol
Exact Mass 530.36073931 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethyl-3-oxospiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-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 + 0.9427 94.27%
Caco-2 - 0.6931 69.31%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8529 85.29%
OATP2B1 inhibitior - 0.7217 72.17%
OATP1B1 inhibitior + 0.8136 81.36%
OATP1B3 inhibitior - 0.3035 30.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6071 60.71%
BSEP inhibitior + 0.9341 93.41%
P-glycoprotein inhibitior + 0.6701 67.01%
P-glycoprotein substrate - 0.6403 64.03%
CYP3A4 substrate + 0.7095 70.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.8201 82.01%
CYP2C9 inhibition - 0.8679 86.79%
CYP2C19 inhibition - 0.8326 83.26%
CYP2D6 inhibition - 0.9621 96.21%
CYP1A2 inhibition - 0.7965 79.65%
CYP2C8 inhibition + 0.6130 61.30%
CYP inhibitory promiscuity - 0.9730 97.30%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6030 60.30%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8958 89.58%
Skin irritation - 0.5866 58.66%
Skin corrosion - 0.8300 83.00%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4077 40.77%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6342 63.42%
skin sensitisation - 0.8905 89.05%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5316 53.16%
Acute Oral Toxicity (c) III 0.3561 35.61%
Estrogen receptor binding + 0.7300 73.00%
Androgen receptor binding + 0.7278 72.78%
Thyroid receptor binding + 0.6178 61.78%
Glucocorticoid receptor binding + 0.7790 77.90%
Aromatase binding + 0.8042 80.42%
PPAR gamma + 0.7016 70.16%
Honey bee toxicity - 0.6697 66.97%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9708 97.08%

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 96.06% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.23% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.10% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.32% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 90.63% 93.04%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.55% 82.69%
CHEMBL259 P32245 Melanocortin receptor 4 89.85% 95.38%
CHEMBL1914 P06276 Butyrylcholinesterase 89.09% 95.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 88.58% 94.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.67% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 85.91% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.22% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.38% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.33% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.83% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.57% 95.89%
CHEMBL5028 O14672 ADAM10 82.11% 97.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.68% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.35% 94.45%

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.
Cleome africana

Cross-Links

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PubChem 74822363
LOTUS LTS0117191
wikiData Q105375566