3beta-Hydroxyfriedelan-16-one

Details

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Internal ID ca2edb0c-00bc-4550-8efa-1c6964b7fdbe
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aS,6aS,6aR,6bS,8aS,9R,10S,12aS,14aS,14bS)-10-hydroxy-2,2,4a,6a,6a,8a,9,14a-octamethyl-3,4,6,6b,7,8,9,10,11,12,12a,13,14,14b-tetradecahydro-1H-picen-5-one
SMILES (Canonical) CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O
SMILES (Isomeric) C[C@H]1[C@H](CC[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC(=O)[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C)C)O
InChI InChI=1S/C30H50O2/c1-19-20(31)9-10-21-26(19,4)12-11-22-27(21,5)15-16-29(7)23-17-25(2,3)13-14-28(23,6)24(32)18-30(22,29)8/h19-23,31H,9-18H2,1-8H3/t19-,20-,21+,22-,23+,26+,27-,28-,29-,30+/m0/s1
InChI Key KAKWUJLNKXBCAN-ULROYCQPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O2
Molecular Weight 442.70 g/mol
Exact Mass 442.381080833 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 8.20
Atomic LogP (AlogP) 7.43
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3beta-Hydroxyfriedelan-16-one

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 + 0.5481 54.81%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7721 77.21%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.9271 92.71%
OATP1B3 inhibitior + 0.9811 98.11%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6750 67.50%
BSEP inhibitior + 0.7305 73.05%
P-glycoprotein inhibitior - 0.7401 74.01%
P-glycoprotein substrate - 0.7602 76.02%
CYP3A4 substrate + 0.6511 65.11%
CYP2C9 substrate - 0.5308 53.08%
CYP2D6 substrate - 0.7538 75.38%
CYP3A4 inhibition - 0.8637 86.37%
CYP2C9 inhibition - 0.7599 75.99%
CYP2C19 inhibition - 0.8480 84.80%
CYP2D6 inhibition - 0.9682 96.82%
CYP1A2 inhibition - 0.6719 67.19%
CYP2C8 inhibition - 0.8082 80.82%
CYP inhibitory promiscuity - 0.9671 96.71%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6536 65.36%
Eye corrosion - 0.9782 97.82%
Eye irritation - 0.9312 93.12%
Skin irritation + 0.6696 66.96%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5650 56.50%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7342 73.42%
skin sensitisation + 0.5716 57.16%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6367 63.67%
Acute Oral Toxicity (c) III 0.8289 82.89%
Estrogen receptor binding + 0.8152 81.52%
Androgen receptor binding + 0.6576 65.76%
Thyroid receptor binding + 0.6433 64.33%
Glucocorticoid receptor binding + 0.8064 80.64%
Aromatase binding + 0.6951 69.51%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8136 81.36%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9563 95.63%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.99% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.80% 82.69%
CHEMBL2581 P07339 Cathepsin D 92.65% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.84% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 88.58% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.54% 97.09%
CHEMBL325 Q13547 Histone deacetylase 1 87.83% 95.92%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.65% 96.38%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.27% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.07% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.11% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.93% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.96% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.87% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.53% 94.45%

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.
Aglaia forbesii
Dendrobium chrysotoxum
Eurybia divaricata
Hydnocarpus hainanensis
Pinus palustris
Piranhea mexicana
Quercus canariensis
Sciadotenia toxifera
Soulamea pancheri
Valeriana microphylla

Cross-Links

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PubChem 101679786
NPASS NPC211899
LOTUS LTS0121185
wikiData Q105137886