Swietmanin B

Details

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Internal ID aea19341-cb3e-431b-8158-ae65211c5e80
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name methyl 2-[(1S,2S,3R,5R,6R,10S,13S,14R,16S)-3,14-diacetyloxy-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-16-yl]acetate
SMILES (Canonical) CC(=O)OC1CC2(C(CC(=O)OC2C3=COC=C3)C4=CC5C(C(C(C(C14)(C5=O)C)CC(=O)OC)(C)C)OC(=O)C)C
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@@]2([C@@H](CC(=O)O[C@H]2C3=COC=C3)C4=C[C@H]5[C@H](C([C@@H]([C@@]([C@@H]14)(C5=O)C)CC(=O)OC)(C)C)OC(=O)C)C
InChI InChI=1S/C31H38O10/c1-15(32)39-21-13-30(5)20(11-24(35)41-27(30)17-8-9-38-14-17)18-10-19-26(36)31(6,25(18)21)22(12-23(34)37-7)29(3,4)28(19)40-16(2)33/h8-10,14,19-22,25,27-28H,11-13H2,1-7H3/t19-,20+,21-,22+,25-,27+,28-,30-,31+/m1/s1
InChI Key OABBIHOSONBHME-FQDANCEYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H38O10
Molecular Weight 570.60 g/mol
Exact Mass 570.24649740 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 4.12
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL1075766

2D Structure

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2D Structure of Swietmanin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 - 0.7401 74.01%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7722 77.22%
OATP2B1 inhibitior - 0.7166 71.66%
OATP1B1 inhibitior - 0.5210 52.10%
OATP1B3 inhibitior + 0.8804 88.04%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9869 98.69%
P-glycoprotein inhibitior + 0.8988 89.88%
P-glycoprotein substrate + 0.6457 64.57%
CYP3A4 substrate + 0.7047 70.47%
CYP2C9 substrate - 0.5962 59.62%
CYP2D6 substrate - 0.8407 84.07%
CYP3A4 inhibition + 0.8432 84.32%
CYP2C9 inhibition - 0.6704 67.04%
CYP2C19 inhibition - 0.7239 72.39%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.8437 84.37%
CYP2C8 inhibition + 0.7054 70.54%
CYP inhibitory promiscuity + 0.5621 56.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4163 41.63%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8806 88.06%
Skin irritation - 0.7168 71.68%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7128 71.28%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6354 63.54%
skin sensitisation - 0.7777 77.77%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6500 65.00%
Acute Oral Toxicity (c) III 0.4093 40.93%
Estrogen receptor binding + 0.8471 84.71%
Androgen receptor binding + 0.7109 71.09%
Thyroid receptor binding + 0.6289 62.89%
Glucocorticoid receptor binding + 0.8382 83.82%
Aromatase binding + 0.6489 64.89%
PPAR gamma + 0.7938 79.38%
Honey bee toxicity - 0.7233 72.33%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9961 99.61%

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 98.90% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.48% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.35% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.20% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 94.02% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.60% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 87.00% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.96% 94.33%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.61% 92.88%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.54% 97.09%
CHEMBL4208 P20618 Proteasome component C5 85.29% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.62% 95.89%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.11% 91.24%
CHEMBL2581 P07339 Cathepsin D 82.97% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.54% 99.23%
CHEMBL3038469 P24941 CDK2/Cyclin A 81.49% 91.38%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.20% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.18% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.99% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.44% 93.00%

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.
Khaya senegalensis
Swietenia mahagoni

Cross-Links

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PubChem 44613295
LOTUS LTS0075864
wikiData Q105188568