Phaeocaulisin E

Details

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Internal ID fad22f06-d6ff-472a-9dec-04fddf6b1044
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (3S,3aS,8S,8aR)-3,8-dihydroxy-3,8-dimethyl-5-propan-2-ylidene-1,2,3a,4,7,8a-hexahydroazulen-6-one
SMILES (Canonical) CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C
SMILES (Isomeric) CC(=C1C[C@H]2[C@@H](CC[C@]2(C)O)[C@@](CC1=O)(C)O)C
InChI InChI=1S/C15H24O3/c1-9(2)10-7-12-11(5-6-14(12,3)17)15(4,18)8-13(10)16/h11-12,17-18H,5-8H2,1-4H3/t11-,12+,14+,15+/m1/s1
InChI Key TXIKNNOOLCGADE-DHMWGJHJSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEMBL2386504
HY-N11570
CS-0649788
E87159
1443040-31-0

2D Structure

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2D Structure of Phaeocaulisin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7790 77.90%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6452 64.52%
OATP2B1 inhibitior - 0.8469 84.69%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.8129 81.29%
P-glycoprotein inhibitior - 0.8863 88.63%
P-glycoprotein substrate - 0.8862 88.62%
CYP3A4 substrate + 0.6202 62.02%
CYP2C9 substrate - 0.8165 81.65%
CYP2D6 substrate - 0.8815 88.15%
CYP3A4 inhibition - 0.8519 85.19%
CYP2C9 inhibition - 0.6487 64.87%
CYP2C19 inhibition - 0.7565 75.65%
CYP2D6 inhibition - 0.9508 95.08%
CYP1A2 inhibition - 0.6231 62.31%
CYP2C8 inhibition - 0.9275 92.75%
CYP inhibitory promiscuity - 0.9008 90.08%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4926 49.26%
Eye corrosion - 0.9889 98.89%
Eye irritation + 0.8257 82.57%
Skin irritation + 0.6379 63.79%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8291 82.91%
skin sensitisation - 0.5805 58.05%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.7262 72.62%
Acute Oral Toxicity (c) I 0.3915 39.15%
Estrogen receptor binding - 0.6872 68.72%
Androgen receptor binding - 0.6142 61.42%
Thyroid receptor binding + 0.5283 52.83%
Glucocorticoid receptor binding - 0.6875 68.75%
Aromatase binding - 0.7257 72.57%
PPAR gamma - 0.8311 83.11%
Honey bee toxicity - 0.9114 91.14%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9737 97.37%

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 96.50% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.92% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.68% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 91.24% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.61% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.84% 91.11%
CHEMBL299 P17252 Protein kinase C alpha 88.27% 98.03%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.38% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.77% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.07% 93.03%
CHEMBL1937 Q92769 Histone deacetylase 2 84.33% 94.75%
CHEMBL2996 Q05655 Protein kinase C delta 83.69% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.70% 99.23%
CHEMBL1902 P62942 FK506-binding protein 1A 82.23% 97.05%
CHEMBL340 P08684 Cytochrome P450 3A4 81.52% 91.19%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.28% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.07% 97.09%

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.
Adiantum capillus-veneris
Curcuma phaeocaulis
Fraxinus quadrangulata
Goniothalamus borneensis
Jacobaea maritima

Cross-Links

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PubChem 14633000
NPASS NPC25908
ChEMBL CHEMBL2386504
LOTUS LTS0078237
wikiData Q105266761