Stypotriol

Details

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Internal ID 41695700-3361-4cd2-8d0f-e7765bf3a4c0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Isocopalane and spongiane diterpenoids
IUPAC Name (2S,4aS,4bR,7S,8S,8aR,10aR)-1,1,4a,7,7',8a-hexamethylspiro[2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-8,2'-3H-1-benzofuran]-2,4',5'-triol
SMILES (Canonical) CC1CCC2C3(CCC(C(C3CCC2(C14CC5=C(O4)C(=CC(=C5O)O)C)C)(C)C)O)C
SMILES (Isomeric) C[C@H]1CC[C@@H]2[C@]3(CC[C@@H](C([C@@H]3CC[C@]2([C@]14CC5=C(O4)C(=CC(=C5O)O)C)C)(C)C)O)C
InChI InChI=1S/C27H40O4/c1-15-13-18(28)22(30)17-14-27(31-23(15)17)16(2)7-8-20-25(5)11-10-21(29)24(3,4)19(25)9-12-26(20,27)6/h13,16,19-21,28-30H,7-12,14H2,1-6H3/t16-,19-,20+,21-,25-,26+,27-/m0/s1
InChI Key HJSZCMVJNUBOQM-JZFVXYNCSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O4
Molecular Weight 428.60 g/mol
Exact Mass 428.29265975 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.73
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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71106-25-7
UNII-E53KF1HF9R
E53KF1HF9R
Stypotriol triacetate
(2S,4aS,4bR,7S,8S,8aR,10aR)-1,1,4a,7,7',8a-hexamethylspiro[2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-8,2'-3H-1-benzofuran]-2,4',5'-triol
(-)-STYPOTRIOL
Q27276878
16,24-CYCLO-13,17-SECOCHOLA-16,20(22),23-TRIENE-3,23,24-TRIOL, 14,17-EPOXY-4,4,8-TRIMETHYL-, (3.BETA.,5.ALPHA.,13.ALPHA.)-
16,24-Cyclo-13,17-secochola-16,20(22),23-triene-3,23,24-triol, 14,17-epoxy-4,4,8-trimethyl-, (3beta,5alpha,13alpha)-
SPIRO(BENZOFURAN-2(3H),1'(2'H)-PHENANTHRENE)-4,5,7'-TRIOL, 3',4',4'A,4'B,5',6',7',8',8'A,9',10',10'A-DODECAHYDRO-2',4'B,7,8',8',10'A-HEXAMETHYL-, (1'S,2'S,4'AR,4'BS,7'S,8'AR,10'AR)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Stypotriol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.5545 55.45%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7168 71.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8840 88.40%
OATP1B3 inhibitior + 0.9160 91.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8071 80.71%
BSEP inhibitior + 0.8405 84.05%
P-glycoprotein inhibitior - 0.6242 62.42%
P-glycoprotein substrate - 0.7885 78.85%
CYP3A4 substrate + 0.6679 66.79%
CYP2C9 substrate - 0.5718 57.18%
CYP2D6 substrate + 0.4195 41.95%
CYP3A4 inhibition - 0.8219 82.19%
CYP2C9 inhibition - 0.8495 84.95%
CYP2C19 inhibition - 0.7418 74.18%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition + 0.6116 61.16%
CYP2C8 inhibition + 0.5886 58.86%
CYP inhibitory promiscuity - 0.8970 89.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5106 51.06%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8860 88.60%
Skin irritation - 0.6273 62.73%
Skin corrosion - 0.9064 90.64%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7454 74.54%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8317 83.17%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.9342 93.42%
Acute Oral Toxicity (c) III 0.4848 48.48%
Estrogen receptor binding + 0.9072 90.72%
Androgen receptor binding + 0.7521 75.21%
Thyroid receptor binding + 0.7206 72.06%
Glucocorticoid receptor binding + 0.8106 81.06%
Aromatase binding + 0.8427 84.27%
PPAR gamma + 0.7347 73.47%
Honey bee toxicity - 0.8583 85.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9870 98.70%

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 99.09% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.37% 93.40%
CHEMBL1951 P21397 Monoamine oxidase A 94.77% 91.49%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.58% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.54% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.37% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.28% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.85% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.31% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.30% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.02% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.36% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.15% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.40% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.42% 90.71%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.38% 85.11%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.32% 90.24%

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.
Catunaregam spinosa

Cross-Links

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PubChem 23424859
NPASS NPC100499
LOTUS LTS0009995
wikiData Q27276878