Bulbocol

Details

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Internal ID 1f51a34f-85b5-4f8c-816f-7344d51cc6f3
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol
SMILES (Canonical) COC1=CC=CC(=C1)CCC2=C(C(=CC(=C2)O)OC)CC3=CC=C(C=C3)O
SMILES (Isomeric) COC1=CC=CC(=C1)CCC2=C(C(=CC(=C2)O)OC)CC3=CC=C(C=C3)O
InChI InChI=1S/C23H24O4/c1-26-21-5-3-4-16(12-21)6-9-18-14-20(25)15-23(27-2)22(18)13-17-7-10-19(24)11-8-17/h3-5,7-8,10-12,14-15,24-25H,6,9,13H2,1-2H3
InChI Key LNSWJKFQNMFNFL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H24O4
Molecular Weight 364.40 g/mol
Exact Mass 364.16745924 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.49
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bulbocol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9574 95.74%
Caco-2 + 0.5723 57.23%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.9468 94.68%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.8157 81.57%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9567 95.67%
P-glycoprotein inhibitior + 0.7324 73.24%
P-glycoprotein substrate + 0.6972 69.72%
CYP3A4 substrate + 0.5834 58.34%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.6471 64.71%
CYP2C9 inhibition - 0.5228 52.28%
CYP2C19 inhibition + 0.8188 81.88%
CYP2D6 inhibition - 0.7585 75.85%
CYP1A2 inhibition + 0.7381 73.81%
CYP2C8 inhibition + 0.9212 92.12%
CYP inhibitory promiscuity + 0.7647 76.47%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6554 65.54%
Carcinogenicity (trinary) Non-required 0.7122 71.22%
Eye corrosion - 0.9726 97.26%
Eye irritation - 0.6216 62.16%
Skin irritation - 0.7842 78.42%
Skin corrosion - 0.8839 88.39%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8719 87.19%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8607 86.07%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6165 61.65%
Acute Oral Toxicity (c) III 0.5972 59.72%
Estrogen receptor binding + 0.9243 92.43%
Androgen receptor binding + 0.8718 87.18%
Thyroid receptor binding + 0.6779 67.79%
Glucocorticoid receptor binding + 0.7847 78.47%
Aromatase binding + 0.6133 61.33%
PPAR gamma + 0.7552 75.52%
Honey bee toxicity - 0.7416 74.16%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9878 98.78%

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
CHEMBL2581 P07339 Cathepsin D 96.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.32% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 95.62% 95.17%
CHEMBL2535 P11166 Glucose transporter 94.14% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.33% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.20% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.16% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.55% 86.33%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.18% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.81% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 90.19% 90.20%
CHEMBL240 Q12809 HERG 89.73% 89.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.54% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.22% 93.99%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.98% 95.89%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 87.16% 95.39%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.59% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.19% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 85.92% 94.73%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.28% 99.18%
CHEMBL4208 P20618 Proteasome component C5 84.09% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.06% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.22% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.97% 86.92%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.18% 92.62%
CHEMBL1921 P47901 Vasopressin V1b receptor 82.03% 92.50%

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.
Gymnadenia conopsea
Pleione bulbocodioides
Pleione formosana

Cross-Links

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PubChem 102316540
NPASS NPC84748
LOTUS LTS0012567
wikiData Q105154473