Friedelane

Details

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Internal ID 6116d5ca-9d37-4114-983e-4a7c0a38f20f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4S,4aR,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene
SMILES (Canonical) CC1CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C
SMILES (Isomeric) C[C@H]1CCC[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C)C
InChI InChI=1S/C30H52/c1-21-10-9-11-22-27(21,5)13-12-23-28(22,6)17-19-30(8)24-20-25(2,3)14-15-26(24,4)16-18-29(23,30)7/h21-24H,9-20H2,1-8H3/t21-,22+,23-,24+,26+,27+,28-,29+,30-/m0/s1
InChI Key KVSNMTUIMXZPLU-XOZXFAFYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C30H52
Molecular Weight 412.70 g/mol
Exact Mass 412.406901659 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 11.60
Atomic LogP (AlogP) 9.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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559-73-9
(4aR,6aR,6bS,8aR,9S,12aR,12bS,14aS,14bR)-2,2,4a,6a,8a,9,12b,14a-octamethyldocosahydropicene
CHEBI:71575
DTXSID001165671
Q27139723
(4beta,5beta,8alpha,9beta,10alpha,13alpha,14beta)-5,9,13-Trimethyl-24,25,26-trinoroleanane
(4S,4aR,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene

2D Structure

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2D Structure of Friedelane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.6257 62.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.7490 74.90%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7114 71.14%
P-glycoprotein inhibitior - 0.7509 75.09%
P-glycoprotein substrate - 0.8691 86.91%
CYP3A4 substrate + 0.5924 59.24%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.7237 72.37%
CYP3A4 inhibition - 0.9174 91.74%
CYP2C9 inhibition - 0.8787 87.87%
CYP2C19 inhibition - 0.8651 86.51%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.8883 88.83%
CYP2C8 inhibition - 0.8514 85.14%
CYP inhibitory promiscuity - 0.8163 81.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5458 54.58%
Eye corrosion - 0.8280 82.80%
Eye irritation - 0.7140 71.40%
Skin irritation - 0.6328 63.28%
Skin corrosion - 0.9237 92.37%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4640 46.40%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation + 0.7891 78.91%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5967 59.67%
Nephrotoxicity - 0.5668 56.68%
Acute Oral Toxicity (c) IV 0.5283 52.83%
Estrogen receptor binding + 0.8827 88.27%
Androgen receptor binding + 0.5965 59.65%
Thyroid receptor binding + 0.6445 64.45%
Glucocorticoid receptor binding + 0.7786 77.86%
Aromatase binding + 0.7461 74.61%
PPAR gamma - 0.5083 50.83%
Honey bee toxicity - 0.7538 75.38%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9970 99.70%

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.12% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.75% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.50% 82.69%
CHEMBL240 Q12809 HERG 93.27% 89.76%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.66% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.60% 97.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 91.10% 95.58%
CHEMBL237 P41145 Kappa opioid receptor 90.85% 98.10%
CHEMBL221 P23219 Cyclooxygenase-1 86.67% 90.17%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.03% 89.05%
CHEMBL1902 P62942 FK506-binding protein 1A 85.38% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.06% 100.00%
CHEMBL2916 O14746 Telomerase reverse transcriptase 84.50% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.75% 94.45%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.31% 91.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.19% 96.09%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.85% 95.27%
CHEMBL204 P00734 Thrombin 82.45% 96.01%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 82.06% 99.17%
CHEMBL1871 P10275 Androgen Receptor 81.70% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.60% 95.89%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.09% 98.99%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.16% 99.18%
CHEMBL259 P32245 Melanocortin receptor 4 80.07% 95.38%

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.
Calophyllum tomentosum
Cremastra appendiculata
Crocus sieberi
Eugenia myrcianthes
Gynochthodes officinalis
Jacobaea persoonii
Montanoa karwinskii
Pongamia pinnata
Salix babylonica
Strychnos decussata
Verbena bonariensis

Cross-Links

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PubChem 15559345
NPASS NPC156342
LOTUS LTS0108770
wikiData Q27139723