Jaborosalactone 31

Details

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Internal ID da0d0d59-a126-4b57-8e8b-f8295f5610e8
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name (1S,3S,4R,9R,10R,12S,13S,16R,17S,19R,24S)-9,10,16-trihydroxy-4,17,20,21,24-pentamethyl-23-oxahexacyclo[11.10.1.01,19.03,12.04,9.016,24]tetracosa-6,20-diene-5,18,22-trione
SMILES (Canonical) CC1C(=O)C2C(=C(C(=O)OC23CC4C(CC(C5(C4(C(=O)C=CC5)C)O)O)C6C3(C1(CC6)O)C)C)C
SMILES (Isomeric) C[C@@H]1C(=O)[C@@H]2C(=C(C(=O)O[C@@]23C[C@H]4[C@@H](C[C@H]([C@@]5([C@@]4(C(=O)C=CC5)C)O)O)[C@H]6[C@]3([C@]1(CC6)O)C)C)C
InChI InChI=1S/C28H36O7/c1-13-14(2)23(32)35-28-12-18-16(11-20(30)27(34)9-6-7-19(29)24(18,27)4)17-8-10-26(33,25(17,28)5)15(3)22(31)21(13)28/h6-7,15-18,20-21,30,33-34H,8-12H2,1-5H3/t15-,16+,17+,18+,20-,21+,24+,25+,26-,27+,28+/m1/s1
InChI Key YMNXFTUYIKXAPW-UGAJVUOVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H36O7
Molecular Weight 484.60 g/mol
Exact Mass 484.24610348 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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CHEMBL500648

2D Structure

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2D Structure of Jaborosalactone 31

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9266 92.66%
Caco-2 - 0.5375 53.75%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7782 77.82%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.8938 89.38%
OATP1B3 inhibitior + 0.9123 91.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7092 70.92%
BSEP inhibitior + 0.6939 69.39%
P-glycoprotein inhibitior - 0.4783 47.83%
P-glycoprotein substrate + 0.5712 57.12%
CYP3A4 substrate + 0.7195 71.95%
CYP2C9 substrate - 0.8178 81.78%
CYP2D6 substrate - 0.8974 89.74%
CYP3A4 inhibition - 0.8904 89.04%
CYP2C9 inhibition - 0.9300 93.00%
CYP2C19 inhibition - 0.8815 88.15%
CYP2D6 inhibition - 0.9562 95.62%
CYP1A2 inhibition - 0.8039 80.39%
CYP2C8 inhibition + 0.5903 59.03%
CYP inhibitory promiscuity - 0.9868 98.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5930 59.30%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9484 94.84%
Skin irritation + 0.6434 64.34%
Skin corrosion - 0.9038 90.38%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7376 73.76%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5324 53.24%
skin sensitisation - 0.8089 80.89%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.4782 47.82%
Acute Oral Toxicity (c) I 0.4679 46.79%
Estrogen receptor binding + 0.8242 82.42%
Androgen receptor binding + 0.7887 78.87%
Thyroid receptor binding + 0.5616 56.16%
Glucocorticoid receptor binding + 0.7998 79.98%
Aromatase binding + 0.7862 78.62%
PPAR gamma + 0.6278 62.78%
Honey bee toxicity - 0.7816 78.16%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9628 96.28%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.40% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.55% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.69% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.20% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.90% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.81% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.54% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.30% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.47% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.42% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.32% 99.23%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.07% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.88% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.24% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.16% 95.89%

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.
Jaborosa rotacea

Cross-Links

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PubChem 44583789
LOTUS LTS0079333
wikiData Q105350654