(1S,4S,5R,8R,10S,13R,14R,17S,18R,23S)-10,23-dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-2-one

Details

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Internal ID 2bf9befd-67f7-4777-90cc-d386a87491da
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1S,4S,5R,8R,10S,13R,14R,17S,18R,23S)-10,23-dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-2-one
SMILES (Canonical) CC1(CCC23C(C1)C4(CCC5C6(CCC(C(C6CCC5(C4(CC2=O)C)C)(C)C)O)C)OC3O)C
SMILES (Isomeric) C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC[C@@]45[C@]3(CC(=O)[C@@]6([C@H]4CC(CC6)(C)C)[C@H](O5)O)C)C)(C)C)O
InChI InChI=1S/C30H48O4/c1-24(2)14-15-29-20(16-24)30(34-23(29)33)13-9-19-26(5)11-10-21(31)25(3,4)18(26)8-12-27(19,6)28(30,7)17-22(29)32/h18-21,23,31,33H,8-17H2,1-7H3/t18-,19+,20+,21-,23-,26-,27+,28-,29+,30-/m0/s1
InChI Key LRSOAEKMGBDUQF-KGJJDTDOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O4
Molecular Weight 472.70 g/mol
Exact Mass 472.35526001 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.88
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4S,5R,8R,10S,13R,14R,17S,18R,23S)-10,23-dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 - 0.5300 53.00%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6923 69.23%
OATP2B1 inhibitior - 0.7163 71.63%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9098 90.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.7211 72.11%
P-glycoprotein inhibitior - 0.6703 67.03%
P-glycoprotein substrate - 0.7846 78.46%
CYP3A4 substrate + 0.6783 67.83%
CYP2C9 substrate - 0.6245 62.45%
CYP2D6 substrate - 0.8076 80.76%
CYP3A4 inhibition - 0.7391 73.91%
CYP2C9 inhibition - 0.8142 81.42%
CYP2C19 inhibition - 0.8204 82.04%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.7476 74.76%
CYP2C8 inhibition - 0.7516 75.16%
CYP inhibitory promiscuity - 0.9665 96.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6251 62.51%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9296 92.96%
Skin irritation + 0.5368 53.68%
Skin corrosion - 0.8884 88.84%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4518 45.18%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6801 68.01%
skin sensitisation - 0.8270 82.70%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.6403 64.03%
Acute Oral Toxicity (c) I 0.4240 42.40%
Estrogen receptor binding + 0.7781 77.81%
Androgen receptor binding + 0.7321 73.21%
Thyroid receptor binding + 0.6367 63.67%
Glucocorticoid receptor binding + 0.7752 77.52%
Aromatase binding + 0.7265 72.65%
PPAR gamma + 0.5740 57.40%
Honey bee toxicity - 0.7464 74.64%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5651 56.51%
Fish aquatic toxicity + 0.9791 97.91%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.37% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.38% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.14% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.98% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.66% 82.69%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.90% 96.61%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.61% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.11% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.82% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.02% 97.14%
CHEMBL259 P32245 Melanocortin receptor 4 83.07% 95.38%
CHEMBL1937 Q92769 Histone deacetylase 2 82.72% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.57% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.21% 95.89%
CHEMBL4302 P08183 P-glycoprotein 1 81.92% 92.98%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.56% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.39% 96.09%
CHEMBL1871 P10275 Androgen Receptor 81.32% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.29% 92.94%

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.
Embelia schimperi

Cross-Links

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PubChem 162845882
LOTUS LTS0266466
wikiData Q105156300