(Z,6S)-6-[(3R,5S,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid

Details

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Internal ID 5c90f86f-f55e-4c76-b241-c2e9cdf4b2cf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (Z,6S)-6-[(3R,5S,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid
SMILES (Canonical) CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CCC(C4(C)C)O)C)C)C
SMILES (Isomeric) C[C@@H](CC/C=C(/C)\C(=O)O)[C@@H]1CC[C@]2([C@]1(CC[C@H]3C2=CC(=O)[C@H]4[C@@]3(CC[C@H](C4(C)C)O)C)C)C
InChI InChI=1S/C30H46O4/c1-18(9-8-10-19(2)26(33)34)20-11-15-30(7)22-17-23(31)25-27(3,4)24(32)13-14-28(25,5)21(22)12-16-29(20,30)6/h10,17-18,20-21,24-25,32H,8-9,11-16H2,1-7H3,(H,33,34)/b19-10-/t18-,20-,21-,24+,25+,28+,29-,30+/m0/s1
InChI Key PIYBJKWSNAZHMU-ZIANZGCQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O4
Molecular Weight 470.70 g/mol
Exact Mass 470.33960994 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.58
H-Bond Acceptor 3
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 (Z,6S)-6-[(3R,5S,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-6-oxo-1,2,3,5,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.4923 49.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8772 87.72%
OATP2B1 inhibitior - 0.7189 71.89%
OATP1B1 inhibitior + 0.7373 73.73%
OATP1B3 inhibitior - 0.3579 35.79%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6032 60.32%
BSEP inhibitior + 0.9225 92.25%
P-glycoprotein inhibitior + 0.6282 62.82%
P-glycoprotein substrate - 0.6047 60.47%
CYP3A4 substrate + 0.6741 67.41%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.9031 90.31%
CYP3A4 inhibition - 0.8336 83.36%
CYP2C9 inhibition - 0.9379 93.79%
CYP2C19 inhibition - 0.9621 96.21%
CYP2D6 inhibition - 0.9619 96.19%
CYP1A2 inhibition - 0.9570 95.70%
CYP2C8 inhibition - 0.7097 70.97%
CYP inhibitory promiscuity - 0.8844 88.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7059 70.59%
Eye corrosion - 0.9957 99.57%
Eye irritation - 0.9546 95.46%
Skin irritation + 0.7169 71.69%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.7337 73.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7030 70.30%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.6491 64.91%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8949 89.49%
Acute Oral Toxicity (c) III 0.6954 69.54%
Estrogen receptor binding + 0.7614 76.14%
Androgen receptor binding + 0.7943 79.43%
Thyroid receptor binding + 0.7346 73.46%
Glucocorticoid receptor binding + 0.8874 88.74%
Aromatase binding + 0.8378 83.78%
PPAR gamma + 0.6417 64.17%
Honey bee toxicity - 0.8470 84.70%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.88% 98.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 93.65% 93.00%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 93.64% 94.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.31% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.63% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 90.33% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.94% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.87% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.04% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.07% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.60% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.02% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.66% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.36% 91.19%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.29% 100.00%
CHEMBL2514 O95665 Neurotensin receptor 2 80.71% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.67% 96.38%

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.
Amphipterygium adstringens

Cross-Links

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PubChem 162980756
LOTUS LTS0164380
wikiData Q105209787