Lepiotaprocerin B

Details

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Internal ID aff4377d-691f-4af9-a4ae-447ec2a86fff
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name methyl (Z,6R)-6-[(1R,3R,4R,5S,7R,11R,16S)-5-acetyloxy-3,7,12,12,16-pentamethyl-13-oxo-18-oxapentacyclo[13.2.1.03,7.08,17.011,16]octadeca-8(17),14-dien-4-yl]-2-methylhept-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H46O6/c1-18(11-10-12-19(2)29(36)37-9)27-22(38-20(3)34)16-31(6)21-13-14-24-30(4,5)25(35)15-26-33(24,8)28(21)23(39-26)17-32(27,31)7/h12,15,18,22-24,27H,10-11,13-14,16-17H2,1-9H3/b19-12-/t18-,22+,23-,24+,27+,31+,32-,33-/m1/s1
InChI Key YVYRIGJMVOARJL-GCGFQLDISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H46O6
Molecular Weight 538.70 g/mol
Exact Mass 538.32943918 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 5.90
Atomic LogP (AlogP) 6.49
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lepiotaprocerin B

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 - 0.6650 66.50%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7634 76.34%
OATP2B1 inhibitior - 0.7190 71.90%
OATP1B1 inhibitior + 0.7773 77.73%
OATP1B3 inhibitior + 0.9236 92.36%
MATE1 inhibitior + 0.6000 60.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9639 96.39%
P-glycoprotein inhibitior + 0.8535 85.35%
P-glycoprotein substrate + 0.6009 60.09%
CYP3A4 substrate + 0.6980 69.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9024 90.24%
CYP3A4 inhibition - 0.6182 61.82%
CYP2C9 inhibition - 0.7661 76.61%
CYP2C19 inhibition - 0.8180 81.80%
CYP2D6 inhibition - 0.9545 95.45%
CYP1A2 inhibition - 0.7457 74.57%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.7453 74.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5894 58.94%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9234 92.34%
Skin irritation - 0.5782 57.82%
Skin corrosion - 0.9298 92.98%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7133 71.33%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.6371 63.71%
skin sensitisation - 0.7986 79.86%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5433 54.33%
Acute Oral Toxicity (c) III 0.5056 50.56%
Estrogen receptor binding + 0.7467 74.67%
Androgen receptor binding + 0.7106 71.06%
Thyroid receptor binding + 0.6472 64.72%
Glucocorticoid receptor binding + 0.8557 85.57%
Aromatase binding + 0.8092 80.92%
PPAR gamma + 0.6697 66.97%
Honey bee toxicity - 0.7058 70.58%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9956 99.56%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.47% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.60% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.04% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.86% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.69% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 89.36% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.43% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.36% 95.56%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.96% 92.88%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.70% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.27% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.26% 91.07%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.69% 94.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.49% 97.25%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.93% 95.71%
CHEMBL221 P23219 Cyclooxygenase-1 83.89% 90.17%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 83.81% 80.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.62% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.79% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.15% 92.62%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.14% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.78% 97.14%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.68% 92.95%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.58% 89.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.50% 99.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.42% 94.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.37% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 146684199
LOTUS LTS0145893
wikiData Q105366307