3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-5-methylidene-14-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid

Details

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Internal ID 5f102fec-4cc7-4a56-8fb0-52f7eaa751ef
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-5-methylidene-14-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid
SMILES (Canonical) CC(CCC=C(C)C=O)C1CCC2(C1(CCC34C2CC5C(C3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C
SMILES (Isomeric) C[C@@H](CC/C=C(\C)/C=O)[C@@H]1CC[C@]2([C@]1(CC[C@@]34[C@@H]2C[C@H]5[C@@H]([C@@]3(C4)CCC(=O)O)C(=C)C(=O)O5)C)C
InChI InChI=1S/C30H42O5/c1-18(16-31)7-6-8-19(2)21-9-11-28(5)23-15-22-25(20(3)26(34)35-22)30(12-10-24(32)33)17-29(23,30)14-13-27(21,28)4/h7,16,19,21-23,25H,3,6,8-15,17H2,1-2,4-5H3,(H,32,33)/b18-7+/t19-,21-,22-,23+,25-,27-,28+,29+,30-/m0/s1
InChI Key YLQIANWVVVMWMO-WOBMAQFHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O5
Molecular Weight 482.60 g/mol
Exact Mass 482.30322444 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.12
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[(1R,3S,4S,8S,10R,11R,14S,15S)-11,15-dimethyl-5-methylidene-14-[(E,2S)-6-methyl-7-oxohept-5-en-2-yl]-6-oxo-7-oxapentacyclo[8.7.0.01,3.04,8.011,15]heptadecan-3-yl]propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 - 0.6671 66.71%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7020 70.20%
OATP2B1 inhibitior - 0.7122 71.22%
OATP1B1 inhibitior + 0.7828 78.28%
OATP1B3 inhibitior + 0.9011 90.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6553 65.53%
BSEP inhibitior + 0.9211 92.11%
P-glycoprotein inhibitior + 0.6302 63.02%
P-glycoprotein substrate + 0.5529 55.29%
CYP3A4 substrate + 0.6905 69.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9049 90.49%
CYP3A4 inhibition + 0.6431 64.31%
CYP2C9 inhibition - 0.8203 82.03%
CYP2C19 inhibition - 0.8696 86.96%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.7668 76.68%
CYP2C8 inhibition + 0.4871 48.71%
CYP inhibitory promiscuity - 0.9223 92.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6466 64.66%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9395 93.95%
Skin irritation + 0.5557 55.57%
Skin corrosion - 0.9108 91.08%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4121 41.21%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6344 63.44%
skin sensitisation - 0.7445 74.45%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7959 79.59%
Acute Oral Toxicity (c) III 0.5281 52.81%
Estrogen receptor binding + 0.7973 79.73%
Androgen receptor binding + 0.7556 75.56%
Thyroid receptor binding + 0.5146 51.46%
Glucocorticoid receptor binding + 0.7853 78.53%
Aromatase binding + 0.7315 73.15%
PPAR gamma + 0.6711 67.11%
Honey bee toxicity - 0.7493 74.93%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9970 99.70%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.91% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.96% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.76% 97.25%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 92.55% 93.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.71% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.63% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 86.01% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.52% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 84.70% 91.19%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.57% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.52% 97.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.50% 95.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.25% 99.23%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.69% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.39% 93.56%
CHEMBL5028 O14672 ADAM10 80.39% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.05% 89.00%

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.
Gardenia sootepensis

Cross-Links

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PubChem 162860654
LOTUS LTS0059477
wikiData Q105350241