Peniciphenalenin B

Details

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Internal ID b03809bd-f2ad-4e48-9547-478f71093745
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name methyl (6R,12R,14R)-4,6,14-trihydroxy-2,12,13,13-tetramethyl-8,15-dioxo-7,11-dioxatetracyclo[7.6.1.05,16.010,14]hexadeca-1(16),2,4,9-tetraene-6-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O9/c1-7-6-9(21)13-11-10(7)14(22)19(25)15(28-8(2)18(19,3)4)12(11)16(23)29-20(13,26)17(24)27-5/h6,8,21,25-26H,1-5H3/t8-,19+,20-/m1/s1
InChI Key DESDOLHJBVTOSK-RFZPYJOHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O9
Molecular Weight 404.40 g/mol
Exact Mass 404.11073221 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Peniciphenalenin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9726 97.26%
Caco-2 - 0.5404 54.04%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7426 74.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8495 84.95%
OATP1B3 inhibitior + 0.9029 90.29%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5988 59.88%
P-glycoprotein inhibitior - 0.6573 65.73%
P-glycoprotein substrate - 0.6595 65.95%
CYP3A4 substrate + 0.6427 64.27%
CYP2C9 substrate - 0.8072 80.72%
CYP2D6 substrate - 0.8740 87.40%
CYP3A4 inhibition + 0.5758 57.58%
CYP2C9 inhibition + 0.6219 62.19%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8097 80.97%
CYP1A2 inhibition - 0.6546 65.46%
CYP2C8 inhibition + 0.5310 53.10%
CYP inhibitory promiscuity + 0.7526 75.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.7058 70.58%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.6249 62.49%
Skin irritation - 0.6921 69.21%
Skin corrosion - 0.9331 93.31%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6693 66.93%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.5576 55.76%
skin sensitisation - 0.7498 74.98%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6715 67.15%
Acute Oral Toxicity (c) III 0.4851 48.51%
Estrogen receptor binding + 0.8387 83.87%
Androgen receptor binding + 0.6916 69.16%
Thyroid receptor binding + 0.6470 64.70%
Glucocorticoid receptor binding + 0.6283 62.83%
Aromatase binding + 0.6685 66.85%
PPAR gamma + 0.6869 68.69%
Honey bee toxicity - 0.8781 87.81%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9784 97.84%

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 98.77% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.54% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 94.75% 83.82%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 92.57% 93.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.40% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.99% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.84% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.66% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.81% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 88.32% 91.19%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.17% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.96% 91.07%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.72% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 86.53% 94.73%
CHEMBL2535 P11166 Glucose transporter 85.07% 98.75%
CHEMBL5028 O14672 ADAM10 84.80% 97.50%
CHEMBL4208 P20618 Proteasome component C5 83.66% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.62% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.96% 97.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.71% 96.21%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.54% 93.40%

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.
There are no matching plants.

Cross-Links

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PubChem 139590992
LOTUS LTS0086263
wikiData Q105103787