Cholesta-22,24-dien-5-ol, 4,4-dimethyl-

Details

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Internal ID 03be0801-17d0-4688-a90a-6f3a20dd1987
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cholestane steroids
IUPAC Name (8S,9S,10R,13R,14S,17R)-4,4,10,13-tetramethyl-17-[(2R,3E)-6-methylhepta-3,5-dien-2-yl]-1,2,3,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-ol
SMILES (Canonical) CC(C=CC=C(C)C)C1CCC2C1(CCC3C2CC(C4C3(CCCC4(C)C)C)O)C
SMILES (Isomeric) C[C@H](/C=C/C=C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(C4[C@@]3(CCCC4(C)C)C)O)C
InChI InChI=1S/C29H48O/c1-19(2)10-8-11-20(3)22-12-13-23-21-18-25(30)26-27(4,5)15-9-16-29(26,7)24(21)14-17-28(22,23)6/h8,10-11,20-26,30H,9,12-18H2,1-7H3/b11-8+/t20-,21+,22-,23+,24+,25?,26?,28-,29-/m1/s1
InChI Key XNAQMJUOONUYMO-LZDVYMBBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O
Molecular Weight 412.70 g/mol
Exact Mass 412.370516150 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.60
Atomic LogP (AlogP) 7.80
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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Cholesta-22,24-dien-5-ol, 4,4-dimethyl-
(22E)-4,4-Dimethylcholesta-22,24-dien-6-ol #

2D Structure

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2D Structure of Cholesta-22,24-dien-5-ol, 4,4-dimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 - 0.5766 57.66%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5704 57.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7433 74.33%
OATP1B3 inhibitior + 0.9140 91.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.5807 58.07%
P-glycoprotein inhibitior - 0.4644 46.44%
P-glycoprotein substrate - 0.7325 73.25%
CYP3A4 substrate + 0.6978 69.78%
CYP2C9 substrate - 0.8255 82.55%
CYP2D6 substrate - 0.7567 75.67%
CYP3A4 inhibition - 0.8715 87.15%
CYP2C9 inhibition - 0.8562 85.62%
CYP2C19 inhibition - 0.7706 77.06%
CYP2D6 inhibition - 0.9534 95.34%
CYP1A2 inhibition - 0.8281 82.81%
CYP2C8 inhibition - 0.7513 75.13%
CYP inhibitory promiscuity - 0.7183 71.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5546 55.46%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9678 96.78%
Skin irritation + 0.7487 74.87%
Skin corrosion - 0.9490 94.90%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6645 66.45%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6162 61.62%
skin sensitisation + 0.6534 65.34%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7892 78.92%
Acute Oral Toxicity (c) III 0.8522 85.22%
Estrogen receptor binding + 0.8423 84.23%
Androgen receptor binding + 0.6366 63.66%
Thyroid receptor binding + 0.6755 67.55%
Glucocorticoid receptor binding + 0.6751 67.51%
Aromatase binding + 0.5885 58.85%
PPAR gamma + 0.6638 66.38%
Honey bee toxicity - 0.6366 63.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9840 98.40%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.10% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.56% 91.11%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 95.26% 95.58%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.70% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 92.78% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.74% 94.45%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 91.91% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.13% 82.69%
CHEMBL236 P41143 Delta opioid receptor 89.51% 99.35%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.57% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.67% 97.09%
CHEMBL237 P41145 Kappa opioid receptor 86.85% 98.10%
CHEMBL1902 P62942 FK506-binding protein 1A 86.53% 97.05%
CHEMBL2581 P07339 Cathepsin D 85.00% 98.95%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 84.77% 95.71%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.49% 93.00%
CHEMBL1871 P10275 Androgen Receptor 84.35% 96.43%
CHEMBL238 Q01959 Dopamine transporter 84.29% 95.88%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.19% 100.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 84.15% 95.69%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.08% 91.03%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.82% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 82.01% 90.17%
CHEMBL268 P43235 Cathepsin K 81.60% 96.85%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.56% 93.56%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.76% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.70% 95.89%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.41% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.24% 100.00%

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.
Eleutherococcus senticosus

Cross-Links

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PubChem 91692434
NPASS NPC5982