(2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]-N-(2-hydroxyethyl)-N-methylacetamide

Details

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Internal ID ddea893e-22d2-4178-9100-0794f9c94da5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]-N-(2-hydroxyethyl)-N-methylacetamide
SMILES (Canonical) CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C)O)C
SMILES (Isomeric) C[C@@H]\1[C@H]2[C@@H](CC/C1=C\C(=O)N(C)CCO)[C@]3(CC[C@@H](C([C@@H]3C[C@@H]2O)(C)C)O)C
InChI InChI=1S/C23H39NO4/c1-14-15(12-20(28)24(5)10-11-25)6-7-16-21(14)17(26)13-18-22(2,3)19(27)8-9-23(16,18)4/h12,14,16-19,21,25-27H,6-11,13H2,1-5H3/b15-12+/t14-,16+,17-,18-,19-,21-,23+/m0/s1
InChI Key TVMAIDIIHRPKGC-AMFKXAKHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H39NO4
Molecular Weight 393.60 g/mol
Exact Mass 393.28790873 g/mol
Topological Polar Surface Area (TPSA) 81.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]-N-(2-hydroxyethyl)-N-methylacetamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9667 96.67%
Caco-2 + 0.6256 62.56%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7202 72.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8773 87.73%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7291 72.91%
BSEP inhibitior + 0.8731 87.31%
P-glycoprotein inhibitior - 0.7198 71.98%
P-glycoprotein substrate - 0.7024 70.24%
CYP3A4 substrate + 0.7044 70.44%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8898 88.98%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8193 81.93%
CYP2C19 inhibition - 0.8694 86.94%
CYP2D6 inhibition - 0.7823 78.23%
CYP1A2 inhibition - 0.9165 91.65%
CYP2C8 inhibition - 0.8488 84.88%
CYP inhibitory promiscuity - 0.8906 89.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6036 60.36%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.9670 96.70%
Skin irritation - 0.7412 74.12%
Skin corrosion - 0.8989 89.89%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4248 42.48%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.7071 70.71%
skin sensitisation - 0.8327 83.27%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.8763 87.63%
Acute Oral Toxicity (c) III 0.6690 66.90%
Estrogen receptor binding + 0.8111 81.11%
Androgen receptor binding + 0.7303 73.03%
Thyroid receptor binding + 0.7702 77.02%
Glucocorticoid receptor binding + 0.8161 81.61%
Aromatase binding + 0.6015 60.15%
PPAR gamma - 0.5691 56.91%
Honey bee toxicity - 0.8128 81.28%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.7816 78.16%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.23% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.14% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 94.30% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.73% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.35% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.71% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.61% 97.25%
CHEMBL237 P41145 Kappa opioid receptor 88.66% 98.10%
CHEMBL204 P00734 Thrombin 87.52% 96.01%
CHEMBL221 P23219 Cyclooxygenase-1 86.78% 90.17%
CHEMBL2581 P07339 Cathepsin D 85.14% 98.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.08% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.20% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.84% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.74% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 83.66% 91.19%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.02% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.49% 90.08%
CHEMBL5028 O14672 ADAM10 80.65% 97.50%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.48% 85.11%

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.
Erythrophleum chlorostachys

Cross-Links

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PubChem 163193430
LOTUS LTS0256324
wikiData Q105265389