(1S,3aS,5aS,5bR,7aR,11aR,11bR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-propan-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13b-dodecahydro-1H-cyclopenta[a]chrysene-3a-carbaldehyde

Details

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Internal ID f4158618-0921-41bc-a6d5-d3e3ec7c9a52
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1S,3aS,5aS,5bR,7aR,11aR,11bR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-propan-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13b-dodecahydro-1H-cyclopenta[a]chrysene-3a-carbaldehyde
SMILES (Canonical) CC(C)C1CCC2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C=O
SMILES (Isomeric) CC(C)[C@@H]1CC[C@]2([C@H]1C3=CC[C@@H]4[C@]5(CCC(=O)C([C@@H]5CC[C@]4([C@@]3(CC2)C)C)(C)C)C)C=O
InChI InChI=1S/C30H46O2/c1-19(2)20-10-15-30(18-31)17-16-28(6)21(25(20)30)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,18-20,22-23,25H,9-17H2,1-7H3/t20-,22-,23+,25+,27-,28+,29+,30+/m0/s1
InChI Key NLHKXQQHNGNPBK-WNYKNMHVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O2
Molecular Weight 438.70 g/mol
Exact Mass 438.349780706 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 7.00
Atomic LogP (AlogP) 7.41
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3aS,5aS,5bR,7aR,11aR,11bR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-propan-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13b-dodecahydro-1H-cyclopenta[a]chrysene-3a-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5281 52.81%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7336 73.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8737 87.37%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6750 67.50%
BSEP inhibitior + 0.9601 96.01%
P-glycoprotein inhibitior - 0.4905 49.05%
P-glycoprotein substrate - 0.7372 73.72%
CYP3A4 substrate + 0.6357 63.57%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7857 78.57%
CYP3A4 inhibition - 0.8800 88.00%
CYP2C9 inhibition - 0.8766 87.66%
CYP2C19 inhibition - 0.5803 58.03%
CYP2D6 inhibition - 0.9529 95.29%
CYP1A2 inhibition - 0.9193 91.93%
CYP2C8 inhibition - 0.5803 58.03%
CYP inhibitory promiscuity - 0.7803 78.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4813 48.13%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9395 93.95%
Skin irritation + 0.5948 59.48%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.5823 58.23%
Human Ether-a-go-go-Related Gene inhibition + 0.6509 65.09%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6155 61.55%
skin sensitisation + 0.7505 75.05%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5743 57.43%
Acute Oral Toxicity (c) III 0.7678 76.78%
Estrogen receptor binding + 0.8138 81.38%
Androgen receptor binding + 0.7435 74.35%
Thyroid receptor binding + 0.7471 74.71%
Glucocorticoid receptor binding + 0.8555 85.55%
Aromatase binding + 0.6544 65.44%
PPAR gamma + 0.7176 71.76%
Honey bee toxicity - 0.8228 82.28%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL1937 Q92769 Histone deacetylase 2 96.09% 94.75%
CHEMBL4072 P07858 Cathepsin B 95.30% 93.67%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 94.61% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.15% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.01% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.55% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.92% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.44% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.57% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.08% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.32% 93.40%
CHEMBL4302 P08183 P-glycoprotein 1 83.99% 92.98%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.87% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.53% 97.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.78% 90.08%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.04% 98.33%
CHEMBL2916 O14746 Telomerase reverse transcriptase 81.29% 90.00%
CHEMBL259 P32245 Melanocortin receptor 4 80.64% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%

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.
Silphium perfoliatum

Cross-Links

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PubChem 14414412
LOTUS LTS0029792
wikiData Q105181339