Kraussianone 4

Details

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Internal ID e2f9cc99-558d-4e56-8751-0fde4a4c6295
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 3-prenylated isoflavanones
IUPAC Name 11,14-dihydroxy-7,7,20,20-tetramethyl-2,6,21,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.017,22]pentacosa-3(12),4,8,10,15(24),16,18,22-octaen-13-one
SMILES (Canonical) CC1(C=CC2=CC3=C(C=C2O1)OC4C3(C(=O)C5=C(O4)C=C6C(=C5O)C=CC(O6)(C)C)O)C
SMILES (Isomeric) CC1(C=CC2=CC3=C(C=C2O1)OC4C3(C(=O)C5=C(O4)C=C6C(=C5O)C=CC(O6)(C)C)O)C
InChI InChI=1S/C25H22O7/c1-23(2)7-5-12-9-14-17(10-15(12)31-23)29-22-25(14,28)21(27)19-18(30-22)11-16-13(20(19)26)6-8-24(3,4)32-16/h5-11,22,26,28H,1-4H3
InChI Key HMLFQVDHVQECID-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H22O7
Molecular Weight 434.40 g/mol
Exact Mass 434.13655304 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Kraussianone 4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9792 97.92%
Caco-2 - 0.6255 62.55%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7849 78.49%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.8600 86.00%
OATP1B3 inhibitior + 0.9124 91.24%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7384 73.84%
P-glycoprotein inhibitior + 0.7472 74.72%
P-glycoprotein substrate - 0.6507 65.07%
CYP3A4 substrate + 0.5964 59.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8453 84.53%
CYP3A4 inhibition - 0.6699 66.99%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.5685 56.85%
CYP2D6 inhibition - 0.8220 82.20%
CYP1A2 inhibition - 0.5336 53.36%
CYP2C8 inhibition - 0.5738 57.38%
CYP inhibitory promiscuity + 0.5485 54.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.5374 53.74%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.5056 50.56%
Skin irritation - 0.6671 66.71%
Skin corrosion - 0.9361 93.61%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7042 70.42%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5051 50.51%
skin sensitisation - 0.7157 71.57%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6277 62.77%
Acute Oral Toxicity (c) III 0.5103 51.03%
Estrogen receptor binding + 0.8283 82.83%
Androgen receptor binding + 0.6693 66.93%
Thyroid receptor binding + 0.7655 76.55%
Glucocorticoid receptor binding + 0.8006 80.06%
Aromatase binding + 0.6052 60.52%
PPAR gamma + 0.8239 82.39%
Honey bee toxicity - 0.8632 86.32%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9887 98.87%

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 98.50% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.44% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.57% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.47% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.92% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.93% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.22% 85.14%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.40% 95.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.86% 96.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.68% 85.11%
CHEMBL1951 P21397 Monoamine oxidase A 83.45% 91.49%
CHEMBL4208 P20618 Proteasome component C5 83.37% 90.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.66% 80.00%

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.
Eriosema kraussianum

Cross-Links

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PubChem 5318852
LOTUS LTS0246159
wikiData Q105030558