(1R,5S,7R,10S,11S,14S,15R,16R,18R,23S)-N,N,10,14,16-pentamethyl-19-propan-2-ylidene-22-azahexacyclo[12.10.0.02,11.05,10.015,23.018,22]tetracos-2-en-7-amine

Details

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Internal ID efa3c45a-fb0b-4853-b3eb-e7b617e92e60
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,5S,7R,10S,11S,14S,15R,16R,18R,23S)-N,N,10,14,16-pentamethyl-19-propan-2-ylidene-22-azahexacyclo[12.10.0.02,11.05,10.015,23.018,22]tetracos-2-en-7-amine
SMILES (Canonical) CC1CC2C(=C(C)C)CCN2C3C1C4(CCC5C(=CCC6C5(CCC(C6)N(C)C)C)C4C3)C
SMILES (Isomeric) C[C@@H]1C[C@@H]2C(=C(C)C)CCN2[C@@H]3[C@H]1[C@]4(CC[C@@H]5C(=CC[C@@H]6[C@@]5(CC[C@H](C6)N(C)C)C)[C@@H]4C3)C
InChI InChI=1S/C31H50N2/c1-19(2)23-12-15-33-27(23)16-20(3)29-28(33)18-26-24-9-8-21-17-22(32(6)7)10-13-30(21,4)25(24)11-14-31(26,29)5/h9,20-22,25-29H,8,10-18H2,1-7H3/t20-,21+,22-,25-,26+,27-,28+,29+,30+,31+/m1/s1
InChI Key DDLGAIMIRZSOGX-IJJBCYRISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H50N2
Molecular Weight 450.70 g/mol
Exact Mass 450.397399603 g/mol
Topological Polar Surface Area (TPSA) 6.50 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.92
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,5S,7R,10S,11S,14S,15R,16R,18R,23S)-N,N,10,14,16-pentamethyl-19-propan-2-ylidene-22-azahexacyclo[12.10.0.02,11.05,10.015,23.018,22]tetracos-2-en-7-amine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9523 95.23%
Caco-2 + 0.6186 61.86%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4433 44.33%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.8735 87.35%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.9374 93.74%
P-glycoprotein inhibitior + 0.6434 64.34%
P-glycoprotein substrate + 0.5923 59.23%
CYP3A4 substrate + 0.7018 70.18%
CYP2C9 substrate - 0.8191 81.91%
CYP2D6 substrate + 0.6000 60.00%
CYP3A4 inhibition - 0.9342 93.42%
CYP2C9 inhibition - 0.8512 85.12%
CYP2C19 inhibition - 0.8879 88.79%
CYP2D6 inhibition - 0.8129 81.29%
CYP1A2 inhibition - 0.8651 86.51%
CYP2C8 inhibition - 0.6636 66.36%
CYP inhibitory promiscuity - 0.7766 77.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6401 64.01%
Eye corrosion - 0.9563 95.63%
Eye irritation - 0.9609 96.09%
Skin irritation - 0.6702 67.02%
Skin corrosion - 0.6442 64.42%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6951 69.51%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.7034 70.34%
skin sensitisation - 0.7753 77.53%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8069 80.69%
Acute Oral Toxicity (c) III 0.6910 69.10%
Estrogen receptor binding + 0.8593 85.93%
Androgen receptor binding + 0.6451 64.51%
Thyroid receptor binding + 0.5327 53.27%
Glucocorticoid receptor binding + 0.7210 72.10%
Aromatase binding + 0.5359 53.59%
PPAR gamma + 0.6842 68.42%
Honey bee toxicity - 0.8100 81.00%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9441 94.41%

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 98.12% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.36% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.21% 82.69%
CHEMBL2581 P07339 Cathepsin D 89.51% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.07% 97.25%
CHEMBL1871 P10275 Androgen Receptor 88.93% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.54% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.54% 92.94%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.26% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.15% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.80% 95.56%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.87% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.56% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.08% 97.09%
CHEMBL261 P00915 Carbonic anhydrase I 81.99% 96.76%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.77% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.25% 95.50%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 80.45% 95.27%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 80.43% 98.99%

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.
There are no matching plants.

Cross-Links

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PubChem 637320
LOTUS LTS0227443
wikiData Q105103714