Dysolenticin B

Details

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Internal ID 2fd1d032-c67d-4f22-b698-4782a993720f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2R)-2-(2-methylprop-1-enyl)-4-[(5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H42O3/c1-18(2)16-19-17-20(26(32)33-19)21-10-14-30(7)23-8-9-24-27(3,4)25(31)12-13-28(24,5)22(23)11-15-29(21,30)6/h8,16-17,19,21-22,24H,9-15H2,1-7H3/t19-,21+,22+,24+,28-,29+,30-/m1/s1
InChI Key RPPAVMFODBKIDO-HALKBXBMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H42O3
Molecular Weight 450.70 g/mol
Exact Mass 450.31339520 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.98
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEBI:68998
CHEMBL1835380
DTXSID801125740
1337973-00-8
Q27137342
rel-(13alpha,14beta,17alpha,23R)-21,23-epoxylanosta-7,20(22),24-triene-3,21-dione
Lanosta-7,20(22),24-trien-21-oic acid, 23-hydroxy-3-oxo-, I(3)-lactone, (13I+/-,14I(2),17I+/-,23R)-

2D Structure

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2D Structure of Dysolenticin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5067 50.67%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7853 78.53%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8650 86.50%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.9568 95.68%
P-glycoprotein inhibitior + 0.8256 82.56%
P-glycoprotein substrate - 0.7418 74.18%
CYP3A4 substrate + 0.6647 66.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9062 90.62%
CYP3A4 inhibition - 0.7037 70.37%
CYP2C9 inhibition - 0.8803 88.03%
CYP2C19 inhibition - 0.6413 64.13%
CYP2D6 inhibition - 0.9541 95.41%
CYP1A2 inhibition - 0.7634 76.34%
CYP2C8 inhibition + 0.4661 46.61%
CYP inhibitory promiscuity - 0.7875 78.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5272 52.72%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9265 92.65%
Skin irritation - 0.5173 51.73%
Skin corrosion - 0.9023 90.23%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6676 66.76%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.6495 64.95%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.6170 61.70%
Acute Oral Toxicity (c) III 0.7185 71.85%
Estrogen receptor binding + 0.8041 80.41%
Androgen receptor binding + 0.7114 71.14%
Thyroid receptor binding + 0.7348 73.48%
Glucocorticoid receptor binding + 0.8535 85.35%
Aromatase binding + 0.7606 76.06%
PPAR gamma + 0.7097 70.97%
Honey bee toxicity - 0.7470 74.70%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.33% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.15% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.28% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 88.92% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.48% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.39% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.69% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.32% 86.33%
CHEMBL2581 P07339 Cathepsin D 80.94% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.10% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.03% 97.25%

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.
Goniocheton lenticellatus

Cross-Links

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PubChem 56601655
NPASS NPC12849
LOTUS LTS0108484
wikiData Q27137342