methyl (1R,2R,4aS,6aR,6aR,6bR,8aR,9S,10S,12aR,14aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylate

Details

Top
Internal ID f016c395-9e44-4510-9c8f-c8b220a0b45a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name methyl (1R,2R,4aS,6aR,6aR,6bR,8aR,9S,10S,12aR,14aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylate
SMILES (Canonical) CC1CCC2(CCC3(C(C2C1(C)O)CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C)C(=O)OC
SMILES (Isomeric) C[C@@H]1CC[C@@]2(CC[C@@]3([C@@H]([C@@H]2[C@]1(C)O)CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H]([C@]5(C)CO)O)C)C)C)C(=O)OC
InChI InChI=1S/C31H52O5/c1-19-10-15-31(25(34)36-7)17-16-28(4)20(24(31)30(19,6)35)8-9-22-26(2)13-12-23(33)27(3,18-32)21(26)11-14-29(22,28)5/h19-24,32-33,35H,8-18H2,1-7H3/t19-,20-,21-,22-,23+,24-,26+,27-,28-,29-,30-,31+/m1/s1
InChI Key FNNTVXQOSBFVNK-LEJBRUQBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C31H52O5
Molecular Weight 504.70 g/mol
Exact Mass 504.38147475 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.35
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of methyl (1R,2R,4aS,6aR,6aR,6bR,8aR,9S,10S,12aR,14aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-4a-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9527 95.27%
Caco-2 - 0.5990 59.90%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7780 77.80%
OATP2B1 inhibitior - 0.5683 56.83%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior - 0.3203 32.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7792 77.92%
BSEP inhibitior + 0.7651 76.51%
P-glycoprotein inhibitior - 0.6545 65.45%
P-glycoprotein substrate - 0.5974 59.74%
CYP3A4 substrate + 0.7213 72.13%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.8176 81.76%
CYP3A4 inhibition - 0.7750 77.50%
CYP2C9 inhibition - 0.7094 70.94%
CYP2C19 inhibition - 0.8709 87.09%
CYP2D6 inhibition - 0.9630 96.30%
CYP1A2 inhibition - 0.7493 74.93%
CYP2C8 inhibition - 0.6130 61.30%
CYP inhibitory promiscuity - 0.9418 94.18%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7496 74.96%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9303 93.03%
Skin irritation - 0.6517 65.17%
Skin corrosion - 0.9695 96.95%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9130 91.30%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7398 73.98%
Acute Oral Toxicity (c) III 0.6149 61.49%
Estrogen receptor binding + 0.6999 69.99%
Androgen receptor binding + 0.7525 75.25%
Thyroid receptor binding + 0.5633 56.33%
Glucocorticoid receptor binding + 0.7406 74.06%
Aromatase binding + 0.6891 68.91%
PPAR gamma + 0.6207 62.07%
Honey bee toxicity - 0.7455 74.55%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9131 91.31%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 98.30% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.37% 96.09%
CHEMBL204 P00734 Thrombin 93.46% 96.01%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.01% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.16% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.94% 96.38%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.57% 92.86%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.20% 96.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 88.04% 94.33%
CHEMBL340 P08684 Cytochrome P450 3A4 87.89% 91.19%
CHEMBL233 P35372 Mu opioid receptor 87.35% 97.93%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.08% 95.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.68% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.13% 91.11%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 85.77% 91.24%
CHEMBL1974 P36888 Tyrosine-protein kinase receptor FLT3 85.61% 91.83%
CHEMBL4072 P07858 Cathepsin B 85.44% 93.67%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.97% 91.07%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 84.89% 87.16%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.48% 95.89%
CHEMBL5028 O14672 ADAM10 82.62% 97.50%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.22% 96.90%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.52% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.28% 95.89%

Plants that contains it

Top
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.
Mussaenda pubescens

Cross-Links

Top
PubChem 162942181
LOTUS LTS0064679
wikiData Q104998403