Fulvinervin B

Details

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Internal ID 00dbd9f4-e894-4553-897a-904203c0bff1
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5-hydroxy-8,8-dimethyl-6-[(1E)-3-methylbuta-1,3-dienyl]-2-phenylpyrano[2,3-h]chromen-4-one
SMILES (Canonical) CC(=C)C=CC1=C2C(=C3C(=C1O)C(=O)C=C(O3)C4=CC=CC=C4)C=CC(O2)(C)C
SMILES (Isomeric) CC(=C)/C=C/C1=C2C(=C3C(=C1O)C(=O)C=C(O3)C4=CC=CC=C4)C=CC(O2)(C)C
InChI InChI=1S/C25H22O4/c1-15(2)10-11-17-22(27)21-19(26)14-20(16-8-6-5-7-9-16)28-24(21)18-12-13-25(3,4)29-23(17)18/h5-14,27H,1H2,2-4H3/b11-10+
InChI Key JJVHZBYZKZAVDJ-ZHACJKMWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H22O4
Molecular Weight 386.40 g/mol
Exact Mass 386.15180918 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.94
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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LMPK12110179

2D Structure

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2D Structure of Fulvinervin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 - 0.6174 61.74%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8131 81.31%
OATP2B1 inhibitior - 0.5797 57.97%
OATP1B1 inhibitior + 0.8762 87.62%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9326 93.26%
P-glycoprotein inhibitior + 0.8806 88.06%
P-glycoprotein substrate - 0.6268 62.68%
CYP3A4 substrate + 0.6242 62.42%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.6780 67.80%
CYP2C9 inhibition + 0.8169 81.69%
CYP2C19 inhibition + 0.9037 90.37%
CYP2D6 inhibition - 0.9163 91.63%
CYP1A2 inhibition - 0.5673 56.73%
CYP2C8 inhibition + 0.7267 72.67%
CYP inhibitory promiscuity + 0.7702 77.02%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.5696 56.96%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.4903 49.03%
Skin irritation - 0.7014 70.14%
Skin corrosion - 0.9486 94.86%
Ames mutagenesis - 0.5164 51.64%
Human Ether-a-go-go-Related Gene inhibition - 0.3700 37.00%
Micronuclear + 0.6359 63.59%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.7095 70.95%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5744 57.44%
Acute Oral Toxicity (c) III 0.6825 68.25%
Estrogen receptor binding + 0.8862 88.62%
Androgen receptor binding + 0.9066 90.66%
Thyroid receptor binding + 0.7361 73.61%
Glucocorticoid receptor binding + 0.8329 83.29%
Aromatase binding + 0.7603 76.03%
PPAR gamma + 0.8429 84.29%
Honey bee toxicity - 0.6998 69.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9946 99.46%

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 99.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.69% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.54% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.29% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.13% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 92.61% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 91.14% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.31% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.98% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 86.08% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.94% 99.23%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.45% 85.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.81% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.53% 94.62%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.42% 95.71%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 80.12% 89.23%

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.
Tephrosia fulvinervis

Cross-Links

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PubChem 44257641
LOTUS LTS0234519
wikiData Q76546329