[(6S,8S,11R,12S,14R,15S,16R)-15-[(1S)-1-aminoethyl]-6-(dimethylamino)-7,7,12,16-tetramethyl-14-tetracyclo[9.7.0.03,8.012,16]octadeca-1(18),2-dienyl] 4-hydroxy-3,5-dimethoxybenzoate

Details

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Internal ID 8695b3dc-bff4-4bfb-aa8d-d1485fbb0df5
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal alkaloids > Buxus alkaloids
IUPAC Name [(6S,8S,11R,12S,14R,15S,16R)-15-[(1S)-1-aminoethyl]-6-(dimethylamino)-7,7,12,16-tetramethyl-14-tetracyclo[9.7.0.03,8.012,16]octadeca-1(18),2-dienyl] 4-hydroxy-3,5-dimethoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H52N2O5/c1-20(36)30-28(42-32(39)23-17-26(40-8)31(38)27(18-23)41-9)19-35(5)25-12-11-24-21(16-22(25)14-15-34(30,35)4)10-13-29(37(6)7)33(24,2)3/h14,16-18,20,24-25,28-30,38H,10-13,15,19,36H2,1-9H3/t20-,24-,25+,28+,29-,30-,34+,35-/m0/s1
InChI Key HGEURJWODKLRBG-ALACSZDWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C35H52N2O5
Molecular Weight 580.80 g/mol
Exact Mass 580.38762276 g/mol
Topological Polar Surface Area (TPSA) 94.30 Ų
XlogP 6.00
Atomic LogP (AlogP) 6.35
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(6S,8S,11R,12S,14R,15S,16R)-15-[(1S)-1-aminoethyl]-6-(dimethylamino)-7,7,12,16-tetramethyl-14-tetracyclo[9.7.0.03,8.012,16]octadeca-1(18),2-dienyl] 4-hydroxy-3,5-dimethoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9716 97.16%
Caco-2 - 0.7452 74.52%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6030 60.30%
OATP2B1 inhibitior - 0.5701 57.01%
OATP1B1 inhibitior + 0.8254 82.54%
OATP1B3 inhibitior + 0.9297 92.97%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9614 96.14%
P-glycoprotein inhibitior + 0.8177 81.77%
P-glycoprotein substrate + 0.7539 75.39%
CYP3A4 substrate + 0.7165 71.65%
CYP2C9 substrate - 0.6023 60.23%
CYP2D6 substrate + 0.3680 36.80%
CYP3A4 inhibition - 0.7582 75.82%
CYP2C9 inhibition - 0.7154 71.54%
CYP2C19 inhibition - 0.7131 71.31%
CYP2D6 inhibition - 0.8245 82.45%
CYP1A2 inhibition - 0.6582 65.82%
CYP2C8 inhibition + 0.7055 70.55%
CYP inhibitory promiscuity - 0.7788 77.88%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5422 54.22%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9274 92.74%
Skin irritation - 0.7381 73.81%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7100 71.00%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8418 84.18%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9313 93.13%
Acute Oral Toxicity (c) III 0.5449 54.49%
Estrogen receptor binding + 0.8306 83.06%
Androgen receptor binding + 0.6971 69.71%
Thyroid receptor binding + 0.6409 64.09%
Glucocorticoid receptor binding + 0.8507 85.07%
Aromatase binding + 0.7757 77.57%
PPAR gamma + 0.7100 71.00%
Honey bee toxicity - 0.7477 74.77%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5218 52.18%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.42% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.41% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.04% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 91.48% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.25% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.68% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.03% 96.21%
CHEMBL204 P00734 Thrombin 88.71% 96.01%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.56% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.56% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.30% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.06% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.97% 92.94%
CHEMBL1871 P10275 Androgen Receptor 84.49% 96.43%
CHEMBL2535 P11166 Glucose transporter 83.68% 98.75%
CHEMBL261 P00915 Carbonic anhydrase I 83.22% 96.76%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.15% 92.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.95% 89.50%
CHEMBL4208 P20618 Proteasome component C5 80.14% 90.00%
CHEMBL1873 P00750 Tissue-type plasminogen activator 80.04% 93.33%

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.
Buxus sempervirens

Cross-Links

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PubChem 163192947
LOTUS LTS0206322
wikiData Q105027707