(3S,5R,9R,10R,13S,14S,17S)-17-[(Z,2S)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

Details

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Internal ID 0a038d3e-42e9-41e6-8576-2d6a34db9592
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,5R,9R,10R,13S,14S,17S)-17-[(Z,2S)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC(CC=CC(C)(C)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C
SMILES (Isomeric) C[C@@H](C/C=C\C(C)(C)O)[C@@H]1CC[C@]2([C@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C
InChI InChI=1S/C30H50O2/c1-20(10-9-16-26(2,3)32)21-13-18-30(8)23-11-12-24-27(4,5)25(31)15-17-28(24,6)22(23)14-19-29(21,30)7/h9,11,16,20-22,24-25,31-32H,10,12-15,17-19H2,1-8H3/b16-9-/t20-,21-,22-,24-,25-,28+,29-,30+/m0/s1
InChI Key UJGVEQGNNKXYLU-ZWERWIPFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O2
Molecular Weight 442.70 g/mol
Exact Mass 442.381080833 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 7.40
Atomic LogP (AlogP) 7.31
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,5R,9R,10R,13S,14S,17S)-17-[(Z,2S)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5570 55.70%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5918 59.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8814 88.14%
OATP1B3 inhibitior + 0.9717 97.17%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9171 91.71%
P-glycoprotein inhibitior - 0.5300 53.00%
P-glycoprotein substrate - 0.6787 67.87%
CYP3A4 substrate + 0.6568 65.68%
CYP2C9 substrate - 0.7657 76.57%
CYP2D6 substrate - 0.7563 75.63%
CYP3A4 inhibition - 0.8517 85.17%
CYP2C9 inhibition - 0.9270 92.70%
CYP2C19 inhibition - 0.8107 81.07%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition - 0.8907 89.07%
CYP2C8 inhibition - 0.5924 59.24%
CYP inhibitory promiscuity - 0.5193 51.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5928 59.28%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9601 96.01%
Skin irritation + 0.5398 53.98%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis - 0.7937 79.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7586 75.86%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6533 65.33%
skin sensitisation + 0.5137 51.37%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.8419 84.19%
Acute Oral Toxicity (c) III 0.6859 68.59%
Estrogen receptor binding + 0.8047 80.47%
Androgen receptor binding + 0.7314 73.14%
Thyroid receptor binding + 0.7556 75.56%
Glucocorticoid receptor binding + 0.8363 83.63%
Aromatase binding + 0.6242 62.42%
PPAR gamma + 0.6051 60.51%
Honey bee toxicity - 0.7987 79.87%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9869 98.69%

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 96.76% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.69% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.61% 96.09%
CHEMBL1977 P11473 Vitamin D receptor 91.33% 99.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.15% 95.89%
CHEMBL2581 P07339 Cathepsin D 90.05% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.00% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.61% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.49% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.07% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.92% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.55% 93.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.44% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.13% 82.69%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 82.35% 91.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.69% 93.56%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.65% 90.24%
CHEMBL226 P30542 Adenosine A1 receptor 80.69% 95.93%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.01% 91.07%

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.
Dysoxylum grande

Cross-Links

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PubChem 56930240
LOTUS LTS0026824
wikiData Q105273936