28-Hydroxylupa-20(29)-ene-3,30-dione

Details

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Internal ID fd8be418-e0d3-493b-a10b-1e5d843863da
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 2-[(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]prop-2-enal
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)CO)C)C)C
SMILES (Isomeric) C[C@@]12CC[C@]3(CC[C@H]([C@@H]3[C@H]1CC[C@H]4[C@]2(CC[C@@H]5[C@@]4(CCC(=O)C5(C)C)C)C)C(=C)C=O)CO
InChI InChI=1S/C30H46O3/c1-19(17-31)20-9-14-30(18-32)16-15-28(5)21(25(20)30)7-8-23-27(4)12-11-24(33)26(2,3)22(27)10-13-29(23,28)6/h17,20-23,25,32H,1,7-16,18H2,2-6H3/t20-,21+,22-,23+,25+,27-,28+,29+,30+/m0/s1
InChI Key VVGUCLDOXVGZMK-CNRMHUMKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O3
Molecular Weight 454.70 g/mol
Exact Mass 454.34469533 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.38
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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SCHEMBL13910818
28-Hydroxylupa-20(29)-ene-3,30-dione

2D Structure

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2D Structure of 28-Hydroxylupa-20(29)-ene-3,30-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 - 0.5992 59.92%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8523 85.23%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8803 88.03%
OATP1B3 inhibitior + 0.8854 88.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.7252 72.52%
BSEP inhibitior + 0.9237 92.37%
P-glycoprotein inhibitior - 0.6715 67.15%
P-glycoprotein substrate - 0.6982 69.82%
CYP3A4 substrate + 0.6654 66.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition - 0.6777 67.77%
CYP2C9 inhibition - 0.7561 75.61%
CYP2C19 inhibition - 0.8627 86.27%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.9151 91.51%
CYP2C8 inhibition + 0.5165 51.65%
CYP inhibitory promiscuity - 0.7829 78.29%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6385 63.85%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9426 94.26%
Skin irritation - 0.5518 55.18%
Skin corrosion - 0.9587 95.87%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6641 66.41%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7921 79.21%
skin sensitisation - 0.7344 73.44%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5252 52.52%
Acute Oral Toxicity (c) III 0.7421 74.21%
Estrogen receptor binding + 0.8274 82.74%
Androgen receptor binding + 0.7933 79.33%
Thyroid receptor binding + 0.6047 60.47%
Glucocorticoid receptor binding + 0.8276 82.76%
Aromatase binding + 0.6978 69.78%
PPAR gamma + 0.6751 67.51%
Honey bee toxicity - 0.8114 81.14%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9961 99.61%

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 92.46% 94.75%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.76% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL204 P00734 Thrombin 90.35% 96.01%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.68% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.13% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.28% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.64% 96.09%
CHEMBL3524 P56524 Histone deacetylase 4 85.98% 92.97%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL233 P35372 Mu opioid receptor 82.29% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.26% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 81.50% 95.38%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.02% 90.08%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.81% 92.94%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.42% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.29% 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.
Microtropis fokienensis
Senegalia mellifera

Cross-Links

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PubChem 641809
NPASS NPC175410
LOTUS LTS0106318
wikiData Q105297663