22,23,24,25-Tetradehydro-simplexin

Details

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Internal ID 6f9d3e57-1e7e-4741-84d2-add68ff922a2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Rhamnofolane and daphnane diterpenoids
IUPAC Name (1R,2R,6S,7S,8R,16R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-[(1E,3E)-nona-1,3-dienyl]-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one
SMILES (Canonical) CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO
SMILES (Isomeric) CCCCC/C=C/C=C/C12OC3C4C5[C@](O5)([C@H]([C@]6([C@H]([C@@]4(O1)[C@@H](C[C@@]3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO
InChI InChI=1S/C30H40O8/c1-6-7-8-9-10-11-12-13-28-36-23-21-24-27(16-31,35-24)25(33)29(34)20(14-18(4)22(29)32)30(21,38-28)19(5)15-26(23,37-28)17(2)3/h10-14,19-21,23-25,31,33-34H,2,6-9,15-16H2,1,3-5H3/b11-10+,13-12+/t19-,20-,21?,23?,24?,25-,26-,27+,28?,29-,30+/m1/s1
InChI Key CZCPFHFUOUQBDL-RNGXKVFMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H40O8
Molecular Weight 528.60 g/mol
Exact Mass 528.27231823 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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22,23,24,25-Tetradehydro-simplexin
C09198

2D Structure

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2D Structure of 22,23,24,25-Tetradehydro-simplexin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8992 89.92%
Caco-2 - 0.7581 75.81%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6519 65.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7960 79.60%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8803 88.03%
P-glycoprotein inhibitior + 0.6864 68.64%
P-glycoprotein substrate + 0.5933 59.33%
CYP3A4 substrate + 0.7012 70.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8571 85.71%
CYP3A4 inhibition - 0.6483 64.83%
CYP2C9 inhibition - 0.7520 75.20%
CYP2C19 inhibition - 0.7768 77.68%
CYP2D6 inhibition - 0.9089 90.89%
CYP1A2 inhibition - 0.7653 76.53%
CYP2C8 inhibition + 0.6147 61.47%
CYP inhibitory promiscuity - 0.8018 80.18%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5760 57.60%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.9304 93.04%
Skin irritation - 0.5868 58.68%
Skin corrosion - 0.9178 91.78%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7152 71.52%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5608 56.08%
skin sensitisation - 0.8498 84.98%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6097 60.97%
Acute Oral Toxicity (c) III 0.5738 57.38%
Estrogen receptor binding + 0.6989 69.89%
Androgen receptor binding + 0.7338 73.38%
Thyroid receptor binding + 0.5852 58.52%
Glucocorticoid receptor binding + 0.7142 71.42%
Aromatase binding + 0.7180 71.80%
PPAR gamma + 0.5467 54.67%
Honey bee toxicity - 0.8493 84.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5702 57.02%
Fish aquatic toxicity + 0.9817 98.17%

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 98.20% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 95.22% 97.79%
CHEMBL2581 P07339 Cathepsin D 93.58% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.82% 96.09%
CHEMBL299 P17252 Protein kinase C alpha 92.48% 98.03%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 91.98% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.97% 99.17%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 90.82% 96.90%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.78% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.51% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.96% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.81% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.30% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.72% 89.00%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 86.17% 92.32%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.90% 94.80%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.65% 90.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.39% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.30% 85.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.95% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.29% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.25% 97.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.10% 89.34%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.23% 86.00%

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.
Diarthron vesiculosum
Excoecaria cochinchinensis
Lasiosiphon kraussianus
Wikstroemia monticola

Cross-Links

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PubChem 118701523
LOTUS LTS0240266
wikiData Q104395594