Phomophyllin F

Details

Top
Internal ID 394cfa46-36d4-4692-8a59-9a152c6dfc22
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Illudanes and illudins
IUPAC Name (2R,7aR,7bR)-2-hydroxy-3,6,6,7b-tetramethyl-1,2,7,7a-tetrahydrocyclobuta[e]inden-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-8-12-11(16)7-15(12,4)10-6-14(2,3)5-9(10)13(8)17/h5,10-11,16H,6-7H2,1-4H3/t10-,11+,15+/m0/s1
InChI Key VYCFKSRAXPXTML-FIXISWKDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
CHEMBL4170448

2D Structure

Top
2D Structure of Phomophyllin F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7768 77.68%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6117 61.17%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9399 93.99%
OATP1B3 inhibitior + 0.9719 97.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8638 86.38%
P-glycoprotein inhibitior - 0.9380 93.80%
P-glycoprotein substrate - 0.8409 84.09%
CYP3A4 substrate + 0.5403 54.03%
CYP2C9 substrate - 0.7411 74.11%
CYP2D6 substrate - 0.8445 84.45%
CYP3A4 inhibition - 0.7535 75.35%
CYP2C9 inhibition - 0.8794 87.94%
CYP2C19 inhibition - 0.7568 75.68%
CYP2D6 inhibition - 0.9273 92.73%
CYP1A2 inhibition - 0.7778 77.78%
CYP2C8 inhibition - 0.9723 97.23%
CYP inhibitory promiscuity - 0.8072 80.72%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8930 89.30%
Carcinogenicity (trinary) Non-required 0.4732 47.32%
Eye corrosion - 0.9823 98.23%
Eye irritation - 0.6642 66.42%
Skin irritation + 0.6750 67.50%
Skin corrosion - 0.9283 92.83%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4198 41.98%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5713 57.13%
skin sensitisation + 0.5836 58.36%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6257 62.57%
Acute Oral Toxicity (c) III 0.7345 73.45%
Estrogen receptor binding - 0.6969 69.69%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5591 55.91%
Glucocorticoid receptor binding - 0.6398 63.98%
Aromatase binding - 0.7874 78.74%
PPAR gamma - 0.6016 60.16%
Honey bee toxicity - 0.8088 80.88%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9699 96.99%

Targets

Top

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.62% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.94% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.69% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.85% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.21% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.79% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.18% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.61% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 81.88% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.29% 89.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.39% 97.33%

Plants that contains it

Top
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

Top
PubChem 139590002
LOTUS LTS0172113
wikiData Q105298880