Bismurrayafoline B

Details

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Internal ID 1b85af7b-1cec-4fb0-8468-857bae98ec73
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2-[1-hydroxy-7-methoxy-3-methyl-8-(3-methylbut-2-enyl)-9H-carbazol-2-yl]-7-methoxy-3-methyl-8-(3-methylbut-2-enyl)-9H-carbazol-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H40N2O4/c1-19(2)9-11-25-29(43-7)15-13-23-27-17-21(5)31(37(41)35(27)39-33(23)25)32-22(6)18-28-24-14-16-30(44-8)26(12-10-20(3)4)34(24)40-36(28)38(32)42/h9-10,13-18,39-42H,11-12H2,1-8H3
InChI Key STVAUJYOJBWBNS-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C38H40N2O4
Molecular Weight 588.70 g/mol
Exact Mass 588.29880776 g/mol
Topological Polar Surface Area (TPSA) 90.50 Ų
XlogP 10.30
Atomic LogP (AlogP) 9.69
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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NSC654279
2-[1-hydroxy-7-methoxy-3-methyl-8-(3-methylbut-2-enyl)-9H-carbazol-2-yl]-7-methoxy-3-methyl-8-(3-methylbut-2-enyl)-9H-carbazol-1-ol
89368-92-3
CHEMBL510968
DTXSID70327413
NSC-654279
NCI60_018843

2D Structure

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2D Structure of Bismurrayafoline 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 - 0.7491 74.91%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7486 74.86%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.8402 84.02%
OATP1B3 inhibitior + 0.9165 91.65%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9845 98.45%
P-glycoprotein inhibitior + 0.8695 86.95%
P-glycoprotein substrate - 0.6210 62.10%
CYP3A4 substrate + 0.5244 52.44%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate + 0.4255 42.55%
CYP3A4 inhibition + 0.6664 66.64%
CYP2C9 inhibition + 0.7252 72.52%
CYP2C19 inhibition + 0.7622 76.22%
CYP2D6 inhibition - 0.5716 57.16%
CYP1A2 inhibition + 0.7831 78.31%
CYP2C8 inhibition + 0.6905 69.05%
CYP inhibitory promiscuity + 0.9310 93.10%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5330 53.30%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.8367 83.67%
Skin irritation - 0.8254 82.54%
Skin corrosion - 0.9349 93.49%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7797 77.97%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6630 66.30%
skin sensitisation - 0.8470 84.70%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.9168 91.68%
Acute Oral Toxicity (c) III 0.6400 64.00%
Estrogen receptor binding + 0.8753 87.53%
Androgen receptor binding + 0.7780 77.80%
Thyroid receptor binding + 0.7091 70.91%
Glucocorticoid receptor binding + 0.7656 76.56%
Aromatase binding + 0.7089 70.89%
PPAR gamma + 0.7293 72.93%
Honey bee toxicity - 0.8885 88.85%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9716 97.16%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.63% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.73% 91.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 93.21% 89.62%
CHEMBL2581 P07339 Cathepsin D 91.63% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.48% 97.21%
CHEMBL1937 Q92769 Histone deacetylase 2 89.94% 94.75%
CHEMBL1951 P21397 Monoamine oxidase A 89.67% 91.49%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.42% 91.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.99% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.80% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.68% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.55% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.80% 86.92%
CHEMBL2535 P11166 Glucose transporter 85.34% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.97% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.89% 99.17%
CHEMBL213 P08588 Beta-1 adrenergic receptor 84.85% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.82% 97.28%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.59% 94.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.21% 92.68%
CHEMBL1255126 O15151 Protein Mdm4 83.72% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.57% 99.15%
CHEMBL255 P29275 Adenosine A2b receptor 82.30% 98.59%
CHEMBL3401 O75469 Pregnane X receptor 81.46% 94.73%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 80.93% 98.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.43% 89.00%
CHEMBL4208 P20618 Proteasome component C5 80.39% 90.00%

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.
Bergera euchrestifolia

Cross-Links

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PubChem 375145
LOTUS LTS0053659
wikiData Q82089206