4Alpha,5Alpha-Epoxybeilschmin B

Details

Top
Internal ID aac1fd7a-9248-46cc-b075-7117d7b2f983
Taxonomy Lignans, neolignans and related compounds > Dibenzylbutane lignans
IUPAC Name (1S,3S,4R,5S)-4,5-dimethyl-1,3-bis(3,4,5-trimethoxyphenyl)-2,6-dioxabicyclo[3.1.0]hexane
SMILES (Canonical) CC1C(OC2(C1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC
SMILES (Isomeric) C[C@@H]1[C@H](O[C@@]2([C@]1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC
InChI InChI=1S/C24H30O8/c1-13-20(14-9-16(25-3)21(29-7)17(10-14)26-4)31-24(23(13,2)32-24)15-11-18(27-5)22(30-8)19(12-15)28-6/h9-13,20H,1-8H3/t13-,20+,23+,24+/m1/s1
InChI Key VPWGVHVPLFYMJZ-POAYHSMPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C24H30O8
Molecular Weight 446.50 g/mol
Exact Mass 446.19406791 g/mol
Topological Polar Surface Area (TPSA) 77.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

Top
4Alpha,5Alpha-Epoxybeilschmin B

2D Structure

Top
2D Structure of 4Alpha,5Alpha-Epoxybeilschmin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9644 96.44%
Caco-2 + 0.7246 72.46%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6688 66.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8984 89.84%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6517 65.17%
P-glycoprotein inhibitior + 0.8022 80.22%
P-glycoprotein substrate - 0.8744 87.44%
CYP3A4 substrate + 0.5415 54.15%
CYP2C9 substrate - 0.8043 80.43%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition + 0.7371 73.71%
CYP2C9 inhibition - 0.7792 77.92%
CYP2C19 inhibition + 0.6956 69.56%
CYP2D6 inhibition - 0.8135 81.35%
CYP1A2 inhibition - 0.7094 70.94%
CYP2C8 inhibition + 0.5364 53.64%
CYP inhibitory promiscuity + 0.7421 74.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4564 45.64%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.7843 78.43%
Skin irritation - 0.7949 79.49%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6420 64.20%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8362 83.62%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4681 46.81%
Acute Oral Toxicity (c) III 0.5022 50.22%
Estrogen receptor binding + 0.8691 86.91%
Androgen receptor binding + 0.6383 63.83%
Thyroid receptor binding + 0.8008 80.08%
Glucocorticoid receptor binding + 0.6478 64.78%
Aromatase binding + 0.5915 59.15%
PPAR gamma + 0.8261 82.61%
Honey bee toxicity - 0.8002 80.02%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9354 93.54%

Targets

Top

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 94.87% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.70% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.36% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 92.27% 97.14%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 89.62% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.80% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.94% 95.56%
CHEMBL4302 P08183 P-glycoprotein 1 86.60% 92.98%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.10% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.75% 96.00%
CHEMBL2535 P11166 Glucose transporter 80.34% 98.75%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.32% 100.00%

Plants that contains it

Top

Cross-Links

Top
PubChem 71459474
NPASS NPC1474
LOTUS LTS0075350
wikiData Q105291056