(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol

Details

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Internal ID 7e9693fc-e884-498e-9cb2-8ae9668ccc34
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Furospirostanes and derivatives
IUPAC Name (1S,2S,4S,5'S,6S,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H44O5/c1-15-23-21(31-27(15)10-9-24(2,14-28)32-27)13-20-18-6-5-16-11-17(29)12-22(30)26(16,4)19(18)7-8-25(20,23)3/h15-23,28-30H,5-14H2,1-4H3/t15-,16-,17-,18+,19-,20-,21-,22+,23-,24-,25-,26-,27-/m0/s1
InChI Key NNPPTPHVNWYNAJ-JREXVZJBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H44O5
Molecular Weight 448.60 g/mol
Exact Mass 448.31887450 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2S,4S,5'S,6S,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8699 86.99%
Caco-2 - 0.6294 62.94%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5666 56.66%
OATP2B1 inhibitior - 0.5689 56.89%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.9213 92.13%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5852 58.52%
BSEP inhibitior - 0.6704 67.04%
P-glycoprotein inhibitior - 0.6871 68.71%
P-glycoprotein substrate - 0.5630 56.30%
CYP3A4 substrate + 0.7190 71.90%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7483 74.83%
CYP3A4 inhibition - 0.8387 83.87%
CYP2C9 inhibition - 0.8934 89.34%
CYP2C19 inhibition - 0.9114 91.14%
CYP2D6 inhibition - 0.9634 96.34%
CYP1A2 inhibition - 0.9086 90.86%
CYP2C8 inhibition + 0.5363 53.63%
CYP inhibitory promiscuity - 0.9229 92.29%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5184 51.84%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9330 93.30%
Skin irritation - 0.5554 55.54%
Skin corrosion - 0.9459 94.59%
Ames mutagenesis - 0.7430 74.30%
Human Ether-a-go-go-Related Gene inhibition - 0.3708 37.08%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6653 66.53%
skin sensitisation - 0.9388 93.88%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8126 81.26%
Acute Oral Toxicity (c) I 0.4739 47.39%
Estrogen receptor binding + 0.7136 71.36%
Androgen receptor binding + 0.5745 57.45%
Thyroid receptor binding + 0.6635 66.35%
Glucocorticoid receptor binding + 0.8159 81.59%
Aromatase binding + 0.7437 74.37%
PPAR gamma + 0.5434 54.34%
Honey bee toxicity - 0.7334 73.34%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8426 84.26%

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 94.92% 96.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 93.04% 89.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.24% 100.00%
CHEMBL1871 P10275 Androgen Receptor 90.64% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 90.27% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.06% 97.09%
CHEMBL299 P17252 Protein kinase C alpha 89.22% 98.03%
CHEMBL2996 Q05655 Protein kinase C delta 88.76% 97.79%
CHEMBL3045 P05771 Protein kinase C beta 87.63% 97.63%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 85.86% 98.46%
CHEMBL204 P00734 Thrombin 85.55% 96.01%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.45% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.83% 95.50%
CHEMBL237 P41145 Kappa opioid receptor 83.55% 98.10%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.37% 96.61%
CHEMBL233 P35372 Mu opioid receptor 82.70% 97.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.21% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.10% 96.95%
CHEMBL4581 P52732 Kinesin-like protein 1 80.73% 93.18%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 80.66% 87.16%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.61% 95.89%

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.
Cordyline rubra
Cordyline stricta

Cross-Links

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PubChem 14412514
LOTUS LTS0056019
wikiData Q105182243