methyl (1R,2S,4aR,4bS,7E,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethylamino]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate

Details

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Internal ID 1ee6ca3c-f0d8-4017-9c17-03726c0a704d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name methyl (1R,2S,4aR,4bS,7E,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethylamino]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate
SMILES (Canonical) CC1C2C(CCC1=CC(=O)NCCN(C)C)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C
SMILES (Isomeric) C[C@@H]\1[C@@H]2[C@H](CC/C1=C\C(=O)NCCN(C)C)[C@]3(CC[C@@H]([C@]([C@@H]3CC2=O)(C)C(=O)OC)O)C
InChI InChI=1S/C25H40N2O5/c1-15-16(13-21(30)26-11-12-27(4)5)7-8-17-22(15)18(28)14-19-24(17,2)10-9-20(29)25(19,3)23(31)32-6/h13,15,17,19-20,22,29H,7-12,14H2,1-6H3,(H,26,30)/b16-13+/t15-,17-,19+,20-,22+,24+,25+/m0/s1
InChI Key TZEBUKDWHLEPOL-HSQRJOBMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H40N2O5
Molecular Weight 448.60 g/mol
Exact Mass 448.29372238 g/mol
Topological Polar Surface Area (TPSA) 95.90 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1R,2S,4aR,4bS,7E,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethylamino]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9361 93.61%
Caco-2 - 0.5275 52.75%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6786 67.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8525 85.25%
OATP1B3 inhibitior + 0.9124 91.24%
MATE1 inhibitior - 0.7326 73.26%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8755 87.55%
P-glycoprotein inhibitior + 0.6314 63.14%
P-glycoprotein substrate + 0.5416 54.16%
CYP3A4 substrate + 0.7441 74.41%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.8259 82.59%
CYP3A4 inhibition - 0.6696 66.96%
CYP2C9 inhibition - 0.7993 79.93%
CYP2C19 inhibition - 0.8439 84.39%
CYP2D6 inhibition - 0.9008 90.08%
CYP1A2 inhibition - 0.8675 86.75%
CYP2C8 inhibition - 0.7395 73.95%
CYP inhibitory promiscuity - 0.9387 93.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.5670 56.70%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9528 95.28%
Skin irritation - 0.7520 75.20%
Skin corrosion - 0.9176 91.76%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6952 69.52%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.7532 75.32%
skin sensitisation - 0.8547 85.47%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8559 85.59%
Acute Oral Toxicity (c) III 0.6579 65.79%
Estrogen receptor binding + 0.7191 71.91%
Androgen receptor binding + 0.7411 74.11%
Thyroid receptor binding + 0.6426 64.26%
Glucocorticoid receptor binding + 0.7694 76.94%
Aromatase binding + 0.6554 65.54%
PPAR gamma - 0.5132 51.32%
Honey bee toxicity - 0.6955 69.55%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5551 55.51%
Fish aquatic toxicity + 0.9395 93.95%

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 98.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.90% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.33% 90.17%
CHEMBL2664 P23526 Adenosylhomocysteinase 88.53% 86.67%
CHEMBL5028 O14672 ADAM10 88.45% 97.50%
CHEMBL226 P30542 Adenosine A1 receptor 87.62% 95.93%
CHEMBL340 P08684 Cytochrome P450 3A4 87.03% 91.19%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.84% 98.75%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 85.59% 97.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.23% 90.08%
CHEMBL233 P35372 Mu opioid receptor 84.86% 97.93%
CHEMBL2996 Q05655 Protein kinase C delta 83.96% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.90% 95.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.15% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.98% 97.09%
CHEMBL1871 P10275 Androgen Receptor 80.83% 96.43%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.58% 85.30%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.46% 89.00%

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.
Cenchrus americanus

Cross-Links

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PubChem 162920305
LOTUS LTS0178306
wikiData Q105268042