Swietmanin H

Details

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Internal ID 382271b0-55fc-4303-a39a-2a0f0ec2590d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name methyl 2-[(1R,2S,5R,6R,13R,14S,16S)-14-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadeca-9,11-dien-16-yl]acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H34O9/c1-15(30)37-25-26(2,3)20(12-21(31)35-6)28(5)18-7-9-27(4)19(17(18)13-29(25,34)24(28)33)11-22(32)38-23(27)16-8-10-36-14-16/h8,10-11,13-14,18,20,23,25,34H,7,9,12H2,1-6H3/t18-,20-,23-,25-,27+,28+,29-/m0/s1
InChI Key KULNKVVPOHFAHL-ZYFLPPHXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O9
Molecular Weight 526.60 g/mol
Exact Mass 526.22028266 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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CHEMBL1081392

2D Structure

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2D Structure of Swietmanin H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 - 0.7268 72.68%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7933 79.33%
OATP2B1 inhibitior - 0.7162 71.62%
OATP1B1 inhibitior - 0.6813 68.13%
OATP1B3 inhibitior - 0.6462 64.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9660 96.60%
P-glycoprotein inhibitior + 0.8383 83.83%
P-glycoprotein substrate + 0.6517 65.17%
CYP3A4 substrate + 0.7088 70.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8847 88.47%
CYP3A4 inhibition + 0.7743 77.43%
CYP2C9 inhibition - 0.7577 75.77%
CYP2C19 inhibition - 0.8559 85.59%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.8471 84.71%
CYP2C8 inhibition + 0.7412 74.12%
CYP inhibitory promiscuity - 0.7682 76.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4313 43.13%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.8885 88.85%
Skin irritation - 0.6428 64.28%
Skin corrosion - 0.9145 91.45%
Ames mutagenesis - 0.6870 68.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6997 69.97%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5781 57.81%
skin sensitisation - 0.8364 83.64%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.5644 56.44%
Acute Oral Toxicity (c) I 0.6311 63.11%
Estrogen receptor binding + 0.8471 84.71%
Androgen receptor binding + 0.7408 74.08%
Thyroid receptor binding + 0.6718 67.18%
Glucocorticoid receptor binding + 0.8345 83.45%
Aromatase binding + 0.6788 67.88%
PPAR gamma + 0.7692 76.92%
Honey bee toxicity - 0.8026 80.26%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9850 98.50%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.44% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.76% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.70% 85.14%
CHEMBL3038469 P24941 CDK2/Cyclin A 90.60% 91.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.75% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 89.50% 94.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.44% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.02% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.00% 89.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 87.66% 91.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.09% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.31% 99.23%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.44% 95.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.12% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.91% 94.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.75% 83.82%
CHEMBL3524 P56524 Histone deacetylase 4 81.31% 92.97%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.16% 86.92%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.04% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.50% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 80.06% 91.19%

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.
Swietenia mahagoni

Cross-Links

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PubChem 44613547
LOTUS LTS0032122
wikiData Q105146216