20S,24S-Epoxy-25-hydroxy-A-homo-4-oxadammaran-3-one

Details

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Internal ID 677ee280-8dd4-41d2-a960-b3a390e727a5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (1R,2R,8R,11R,12R,15S,16R)-15-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-2,7,7,11,12-pentamethyl-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-5-one
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C
SMILES (Isomeric) C[C@@]12CC[C@@H]([C@H]1CC[C@H]3[C@]2(CC[C@@H]4[C@@]3(CCC(=O)OC4(C)C)C)C)[C@@]5(CC[C@H](O5)C(C)(C)O)C
InChI InChI=1S/C30H50O4/c1-25(2,32)23-13-18-30(8,33-23)20-11-16-28(6)19(20)9-10-22-27(5)15-14-24(31)34-26(3,4)21(27)12-17-29(22,28)7/h19-23,32H,9-18H2,1-8H3/t19-,20+,21+,22-,23+,27+,28-,29-,30+/m1/s1
InChI Key ZHWDSUNHEWADAB-YUOZJKDKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O4
Molecular Weight 474.70 g/mol
Exact Mass 474.37091007 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.68
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEBI:70459
20S,24S-Epoxy-25-hydroxy-A-homo-4-oxadammaran-3-one
BDBM50335581
Q27138796
(20S,24S)-20,24-Epoxy-25-hydroxy-A-homo-4-oxadammarane-3-one
(20S*,24S*)-25-Hydroxy-20,24-epoxy-A-homo-4-oxadammaran- 3-one

2D Structure

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2D Structure of 20S,24S-Epoxy-25-hydroxy-A-homo-4-oxadammaran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 - 0.5710 57.10%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8182 81.82%
OATP2B1 inhibitior - 0.7095 70.95%
OATP1B1 inhibitior + 0.8940 89.40%
OATP1B3 inhibitior + 0.8299 82.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6108 61.08%
BSEP inhibitior + 0.6952 69.52%
P-glycoprotein inhibitior - 0.5217 52.17%
P-glycoprotein substrate - 0.7798 77.98%
CYP3A4 substrate + 0.7107 71.07%
CYP2C9 substrate - 0.6250 62.50%
CYP2D6 substrate - 0.8573 85.73%
CYP3A4 inhibition - 0.7393 73.93%
CYP2C9 inhibition - 0.8138 81.38%
CYP2C19 inhibition - 0.7488 74.88%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.7898 78.98%
CYP2C8 inhibition + 0.4674 46.74%
CYP inhibitory promiscuity - 0.9485 94.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5898 58.98%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9243 92.43%
Skin irritation - 0.5917 59.17%
Skin corrosion - 0.8881 88.81%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3659 36.59%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7676 76.76%
skin sensitisation - 0.8551 85.51%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7445 74.45%
Acute Oral Toxicity (c) III 0.5163 51.63%
Estrogen receptor binding + 0.7077 70.77%
Androgen receptor binding + 0.7374 73.74%
Thyroid receptor binding + 0.6089 60.89%
Glucocorticoid receptor binding + 0.7965 79.65%
Aromatase binding + 0.6609 66.09%
PPAR gamma + 0.5459 54.59%
Honey bee toxicity - 0.7929 79.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9839 98.39%

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 93.98% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.46% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.57% 95.56%
CHEMBL1871 P10275 Androgen Receptor 88.50% 96.43%
CHEMBL2581 P07339 Cathepsin D 87.56% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.43% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.25% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.75% 93.04%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.14% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.11% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 84.15% 94.75%
CHEMBL4040 P28482 MAP kinase ERK2 84.03% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.91% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.55% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.48% 89.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.72% 92.88%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.10% 92.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.21% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.97% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.77% 86.33%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.73% 90.93%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 80.40% 100.00%

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.
Aglaia foveolata
Cinnamomum aromaticum

Cross-Links

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PubChem 53318969
NPASS NPC148740
LOTUS LTS0144443
wikiData Q27138796