Glabcensin W

Details

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Internal ID 8b1d743f-ccec-43e2-8dcd-fbc519caff54
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1R,2R,3R,4S,6S,9S,10S,11S,13S)-2,3,11-triacetyloxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical) CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)OC(=O)C)C
SMILES (Isomeric) CC(=O)O[C@H]1CC[C@]2([C@@H]3[C@H](C[C@@H]4C[C@@]3([C@H]([C@@H]([C@@H]2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)OC(=O)C)C
InChI InChI=1S/C28H38O9/c1-13-18-11-19(34-14(2)29)22-27(8)10-9-20(35-15(3)30)26(6,7)23(27)21(36-16(4)31)25(37-17(5)32)28(22,12-18)24(13)33/h18-23,25H,1,9-12H2,2-8H3/t18-,19+,20+,21-,22+,23-,25+,27+,28+/m1/s1
InChI Key ZKBSGYHEBWMFOE-QOCFDZAGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H38O9
Molecular Weight 518.60 g/mol
Exact Mass 518.25158279 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Glabcensin W

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 - 0.6660 66.60%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7049 70.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8851 88.51%
OATP1B3 inhibitior + 0.7898 78.98%
MATE1 inhibitior - 0.5000 50.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7950 79.50%
P-glycoprotein inhibitior + 0.8047 80.47%
P-glycoprotein substrate - 0.7475 74.75%
CYP3A4 substrate + 0.6957 69.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8778 87.78%
CYP3A4 inhibition - 0.7300 73.00%
CYP2C9 inhibition - 0.7682 76.82%
CYP2C19 inhibition - 0.7603 76.03%
CYP2D6 inhibition - 0.9486 94.86%
CYP1A2 inhibition - 0.7290 72.90%
CYP2C8 inhibition - 0.6380 63.80%
CYP inhibitory promiscuity - 0.9046 90.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5665 56.65%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8314 83.14%
Skin irritation + 0.5225 52.25%
Skin corrosion - 0.9307 93.07%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5500 55.00%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.6300 63.00%
skin sensitisation - 0.6135 61.35%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6133 61.33%
Acute Oral Toxicity (c) III 0.5244 52.44%
Estrogen receptor binding + 0.8477 84.77%
Androgen receptor binding + 0.6658 66.58%
Thyroid receptor binding + 0.6097 60.97%
Glucocorticoid receptor binding + 0.7660 76.60%
Aromatase binding + 0.6879 68.79%
PPAR gamma + 0.7653 76.53%
Honey bee toxicity - 0.7681 76.81%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.84% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.03% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.51% 82.69%
CHEMBL340 P08684 Cytochrome P450 3A4 91.17% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.96% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 86.19% 95.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.18% 91.11%
CHEMBL2581 P07339 Cathepsin D 85.14% 98.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.06% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.81% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 82.70% 92.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.52% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.33% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.21% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.95% 95.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.90% 94.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.86% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.04% 99.23%

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.
Isodon angustifolius

Cross-Links

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PubChem 5317642
LOTUS LTS0023396
wikiData Q105378355