Beauvenniatin A

Details

Top
Internal ID c6d36e68-2fdf-47f6-98ea-aa5782fad52a
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (3S,6R,9S,12R,15S,18R)-3,9-dibenzyl-4,10,16-trimethyl-6,12,15,18-tetra(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H57N3O9/c1-24(2)32-41(50)53-34(26(5)6)37(46)43(10)30(22-28-18-14-12-15-19-28)39(48)51-33(25(3)4)36(45)42(9)31(23-29-20-16-13-17-21-29)40(49)52-35(27(7)8)38(47)44(32)11/h12-21,24-27,30-35H,22-23H2,1-11H3/t30-,31-,32-,33+,34+,35+/m0/s1
InChI Key DUOXILOCBMQICJ-DULUVLRMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C41H57N3O9
Molecular Weight 735.90 g/mol
Exact Mass 735.40948040 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Beauvenniatin A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8161 81.61%
Caco-2 - 0.7248 72.48%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5227 52.27%
OATP2B1 inhibitior - 0.5739 57.39%
OATP1B1 inhibitior + 0.9035 90.35%
OATP1B3 inhibitior + 0.9295 92.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9502 95.02%
P-glycoprotein inhibitior + 0.8625 86.25%
P-glycoprotein substrate - 0.6250 62.50%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.7242 72.42%
CYP2C9 inhibition - 0.8284 82.84%
CYP2C19 inhibition - 0.7855 78.55%
CYP2D6 inhibition - 0.9455 94.55%
CYP1A2 inhibition - 0.9164 91.64%
CYP2C8 inhibition - 0.9504 95.04%
CYP inhibitory promiscuity - 0.8578 85.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7707 77.07%
Carcinogenicity (trinary) Non-required 0.6228 62.28%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9291 92.91%
Skin irritation - 0.7938 79.38%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6572 65.72%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.9102 91.02%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7837 78.37%
Nephrotoxicity - 0.7222 72.22%
Acute Oral Toxicity (c) III 0.7271 72.71%
Estrogen receptor binding + 0.7132 71.32%
Androgen receptor binding + 0.6571 65.71%
Thyroid receptor binding + 0.5561 55.61%
Glucocorticoid receptor binding + 0.7440 74.40%
Aromatase binding + 0.5279 52.79%
PPAR gamma + 0.7185 71.85%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8400 84.00%

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
CHEMBL2581 P07339 Cathepsin D 98.98% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.31% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.82% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.29% 85.14%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.03% 85.94%
CHEMBL1978 P11511 Cytochrome P450 19A1 86.96% 91.76%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.87% 97.25%
CHEMBL4072 P07858 Cathepsin B 82.44% 93.67%
CHEMBL3401 O75469 Pregnane X receptor 82.27% 94.73%
CHEMBL3891 P07384 Calpain 1 80.65% 93.04%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 54768788
LOTUS LTS0197855
wikiData Q75065076