Biexcisusin A, (rel)-

Details

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Internal ID 0a64ba49-c93c-440a-a88e-9a91866d88e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(1S,3S,4R,6S,8S,9R,10S,11S,13R,14S)-6-acetyloxy-14-[2-[(1S,3S,4R,6S,8S,9R,10S,11S,13R,14S)-6,8-diacetyloxy-3,11,14-trihydroxy-5,5,9-trimethyl-15-oxo-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]ethyl]-3,8,14-trihydroxy-5,5,9-trimethyl-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C48H70O16/c1-21(49)61-30-14-26-18-46(20-28(54)35-41(5,6)32(62-22(2)50)15-31(56)43(35,9)38(30)46)40(58)48(26,60)12-11-47(59)25-13-27(53)37-44(10)34(64-24(4)52)16-33(63-23(3)51)42(7,8)36(44)29(55)19-45(37,17-25)39(47)57/h25-38,53-56,59-60H,11-20H2,1-10H3/t25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35+,36+,37-,38-,43+,44+,45-,46-,47-,48-/m0/s1
InChI Key XZEKVUGXYUJKNA-VMAKWLQMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C48H70O16
Molecular Weight 903.10 g/mol
Exact Mass 902.46638614 g/mol
Topological Polar Surface Area (TPSA) 261.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 16
H-Bond Donor 6
Rotatable Bonds 7

Synonyms

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CHEMBL1941084
CHEBI:68975
Q27137326

2D Structure

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2D Structure of Biexcisusin A, (rel)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9709 97.09%
Caco-2 - 0.8598 85.98%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8258 82.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8759 87.59%
OATP1B3 inhibitior + 0.8658 86.58%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7369 73.69%
P-glycoprotein inhibitior + 0.7578 75.78%
P-glycoprotein substrate + 0.5292 52.92%
CYP3A4 substrate + 0.7002 70.02%
CYP2C9 substrate - 0.8277 82.77%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition - 0.8123 81.23%
CYP2C19 inhibition - 0.7274 72.74%
CYP2D6 inhibition - 0.9684 96.84%
CYP1A2 inhibition - 0.8191 81.91%
CYP2C8 inhibition - 0.6176 61.76%
CYP inhibitory promiscuity - 0.9640 96.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7213 72.13%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9011 90.11%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition - 0.3986 39.86%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5008 50.08%
skin sensitisation - 0.8617 86.17%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5821 58.21%
Acute Oral Toxicity (c) I 0.3551 35.51%
Estrogen receptor binding + 0.7636 76.36%
Androgen receptor binding + 0.7355 73.55%
Thyroid receptor binding + 0.5230 52.30%
Glucocorticoid receptor binding + 0.7721 77.21%
Aromatase binding + 0.6548 65.48%
PPAR gamma + 0.7637 76.37%
Honey bee toxicity - 0.6806 68.06%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9806 98.06%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.62% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.89% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.32% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.00% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 89.35% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.15% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.49% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.00% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.54% 91.07%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.98% 82.69%
CHEMBL259 P32245 Melanocortin receptor 4 82.17% 95.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.74% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.29% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.15% 97.28%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.05% 89.00%

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.
Isodon excisus

Cross-Links

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PubChem 57393032
LOTUS LTS0140344
wikiData Q27137326