Dihydrolupeol

Details

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Internal ID 2258f980-6670-481c-aa63-ef2a22391756
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1S,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol
SMILES (Canonical) CC(C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C
SMILES (Isomeric) CC(C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@@H]4[C@]5(CC[C@@H](C([C@@H]5CC[C@]4([C@@]3(CC2)C)C)(C)C)O)C)C
InChI InChI=1S/C30H52O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h19-25,31H,9-18H2,1-8H3/t20-,21+,22-,23+,24-,25+,27+,28-,29+,30+/m0/s1
InChI Key UBLNLUPLUKPSPP-QGTGJCAVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H52O
Molecular Weight 428.70 g/mol
Exact Mass 428.401816278 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.90
Atomic LogP (AlogP) 8.10
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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dihydrolupeol
5alpha-Lupan-3beta-ol
(3beta)-Lupan-3-ol
SCHEMBL476920
DTXSID801317117

2D Structure

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2D Structure of Dihydrolupeol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 - 0.5305 53.05%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4957 49.57%
OATP2B1 inhibitior - 0.5863 58.63%
OATP1B1 inhibitior + 0.9367 93.67%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7819 78.19%
P-glycoprotein substrate - 0.8751 87.51%
CYP3A4 substrate + 0.6603 66.03%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate + 0.3527 35.27%
CYP3A4 inhibition - 0.9232 92.32%
CYP2C9 inhibition - 0.7296 72.96%
CYP2C19 inhibition - 0.8298 82.98%
CYP2D6 inhibition - 0.9712 97.12%
CYP1A2 inhibition - 0.6166 61.66%
CYP2C8 inhibition - 0.7687 76.87%
CYP inhibitory promiscuity - 0.9145 91.45%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6216 62.16%
Eye corrosion - 0.9722 97.22%
Eye irritation - 0.8165 81.65%
Skin irritation + 0.7394 73.94%
Skin corrosion - 0.8860 88.60%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5639 56.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7999 79.99%
skin sensitisation + 0.5829 58.29%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8091 80.91%
Acute Oral Toxicity (c) III 0.8025 80.25%
Estrogen receptor binding + 0.8044 80.44%
Androgen receptor binding + 0.7530 75.30%
Thyroid receptor binding + 0.6377 63.77%
Glucocorticoid receptor binding + 0.7821 78.21%
Aromatase binding + 0.7057 70.57%
PPAR gamma - 0.4891 48.91%
Honey bee toxicity - 0.6789 67.89%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9570 95.70%

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.23% 96.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.36% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 92.87% 94.75%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 91.14% 95.58%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.57% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.69% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 89.44% 90.17%
CHEMBL204 P00734 Thrombin 88.83% 96.01%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.71% 96.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 88.38% 91.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.57% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.32% 96.61%
CHEMBL4302 P08183 P-glycoprotein 1 87.29% 92.98%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.44% 92.86%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.17% 100.00%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 85.36% 99.00%
CHEMBL237 P41145 Kappa opioid receptor 85.35% 98.10%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.42% 97.09%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 83.94% 99.17%
CHEMBL2179 P04062 Beta-glucocerebrosidase 83.37% 85.31%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.14% 99.18%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.95% 92.88%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.28% 98.99%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.64% 97.50%

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.
Agathosma scaberula
Balanophora harlandii
Cassia fistula
Cichorium intybus
Euphorbia nicaeensis
Lupinus cosentinii
Polemonium caeruleum
Strychnos ledermannii
Viburnum davidii
Wunderlichia mirabilis

Cross-Links

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PubChem 13458955
NPASS NPC57233
LOTUS LTS0219524
wikiData Q104888675