18alpha-Oleanane

Details

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Internal ID 954a7993-1b96-4042-8aa6-9ba49b2163c5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aS,6aR,6aR,6bR,8aR,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene
SMILES (Canonical) CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C
SMILES (Isomeric) C[C@@]12CC[C@@]3([C@@H]([C@H]1CC(CC2)(C)C)CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CCCC5(C)C)C)C)C
InChI InChI=1S/C30H52/c1-25(2)16-17-27(5)18-19-29(7)21(22(27)20-25)10-11-24-28(6)14-9-13-26(3,4)23(28)12-15-30(24,29)8/h21-24H,9-20H2,1-8H3/t21-,22-,23+,24-,27-,28+,29-,30-/m1/s1
InChI Key VCNKUCWWHVTTBY-UFBHZMJMSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C30H52
Molecular Weight 412.70 g/mol
Exact Mass 412.406901659 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 11.60
Atomic LogP (AlogP) 9.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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30759-92-3
Oleanane, (18.alpha.)-
Germanicane
(18alpha)-Oleanane
18.alpha.-Oleanane
DTXSID301019528
(4aS,6aR,6aR,6bR,8aR,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene

2D Structure

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2D Structure of 18alpha-Oleanane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.5886 58.86%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.7490 74.90%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9113 91.13%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7025 70.25%
P-glycoprotein inhibitior - 0.7400 74.00%
P-glycoprotein substrate - 0.8919 89.19%
CYP3A4 substrate + 0.6258 62.58%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.7237 72.37%
CYP3A4 inhibition - 0.9174 91.74%
CYP2C9 inhibition - 0.8787 87.87%
CYP2C19 inhibition - 0.8651 86.51%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.8883 88.83%
CYP2C8 inhibition - 0.6466 64.66%
CYP inhibitory promiscuity - 0.8163 81.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5458 54.58%
Eye corrosion - 0.8280 82.80%
Eye irritation - 0.7048 70.48%
Skin irritation - 0.6328 63.28%
Skin corrosion - 0.9237 92.37%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3986 39.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.7891 78.91%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5967 59.67%
Nephrotoxicity - 0.6766 67.66%
Acute Oral Toxicity (c) IV 0.5283 52.83%
Estrogen receptor binding + 0.8789 87.89%
Androgen receptor binding + 0.6572 65.72%
Thyroid receptor binding + 0.6106 61.06%
Glucocorticoid receptor binding + 0.8235 82.35%
Aromatase binding + 0.7147 71.47%
PPAR gamma + 0.5378 53.78%
Honey bee toxicity - 0.7383 73.83%
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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.61% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.49% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.41% 97.09%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 92.36% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.21% 94.45%
CHEMBL5203 P33316 dUTP pyrophosphatase 91.43% 99.18%
CHEMBL4302 P08183 P-glycoprotein 1 88.75% 92.98%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.26% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.51% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.42% 95.89%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 87.05% 98.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.02% 96.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.83% 91.03%
CHEMBL1937 Q92769 Histone deacetylase 2 85.42% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.39% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.20% 96.61%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.80% 92.88%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.54% 94.78%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 81.33% 88.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.04% 91.11%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 80.84% 99.17%
CHEMBL259 P32245 Melanocortin receptor 4 80.79% 95.38%
CHEMBL204 P00734 Thrombin 80.21% 96.01%

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.
Acacia pruinosa
Aegilops geniculata
Cycas beddomei
Iodes cirrhosa
Kalanchoe pinnata
Lespedeza davidii
Syzygium samarangense

Cross-Links

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PubChem 12306152
NPASS NPC61535
LOTUS LTS0156136
wikiData Q105283830