Leucophyllin D

Details

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Internal ID 1fb7a90e-1b65-483e-8901-525cb5107a2f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,8-diacetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical) CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(=O)C4=C)O)C)OC(=O)C
SMILES (Isomeric) CC(=O)O[C@H]1C[C@@H](C([C@@H]2[C@@]1([C@@H]3[C@H](C[C@@H]4C[C@@]3([C@H]([C@@H]2O)OC(=O)C)C(=O)C4=C)O)C)(C)C)OC(=O)C
InChI InChI=1S/C26H36O9/c1-11-15-8-16(30)20-25(7)18(34-13(3)28)9-17(33-12(2)27)24(5,6)21(25)19(31)23(35-14(4)29)26(20,10-15)22(11)32/h15-21,23,30-31H,1,8-10H2,2-7H3/t15-,16+,17+,18+,19-,20+,21-,23+,25+,26+/m1/s1
InChI Key CUCNENMUNUSTEG-LYVLPCRDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H36O9
Molecular Weight 492.60 g/mol
Exact Mass 492.23593272 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Leucophyllin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9854 98.54%
Caco-2 - 0.7278 72.78%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6967 69.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8737 87.37%
OATP1B3 inhibitior + 0.8350 83.50%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7561 75.61%
P-glycoprotein inhibitior - 0.4931 49.31%
P-glycoprotein substrate - 0.7243 72.43%
CYP3A4 substrate + 0.6438 64.38%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.7792 77.92%
CYP2C9 inhibition - 0.8476 84.76%
CYP2C19 inhibition - 0.7946 79.46%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition - 0.8220 82.20%
CYP2C8 inhibition - 0.6515 65.15%
CYP inhibitory promiscuity - 0.9085 90.85%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5998 59.98%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8900 89.00%
Skin irritation + 0.5052 50.52%
Skin corrosion - 0.9332 93.32%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5681 56.81%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6042 60.42%
skin sensitisation - 0.6217 62.17%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.8161 81.61%
Acute Oral Toxicity (c) I 0.4788 47.88%
Estrogen receptor binding + 0.7902 79.02%
Androgen receptor binding + 0.6364 63.64%
Thyroid receptor binding - 0.5138 51.38%
Glucocorticoid receptor binding + 0.7287 72.87%
Aromatase binding + 0.7233 72.33%
PPAR gamma + 0.6482 64.82%
Honey bee toxicity - 0.6299 62.99%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9947 99.47%

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 96.27% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.14% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.96% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 89.34% 91.19%
CHEMBL2581 P07339 Cathepsin D 88.80% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.02% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.68% 97.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.61% 95.50%
CHEMBL259 P32245 Melanocortin receptor 4 83.54% 95.38%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.38% 91.07%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.31% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.28% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.21% 86.33%

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.
Isodon leucophyllus

Cross-Links

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PubChem 101938884
NPASS NPC44958
LOTUS LTS0191387
wikiData Q104970165