Super Squalene; trans-Squalene;AddaVax

Details

Top
Internal ID 1189cd51-2e92-4d90-85aa-caf66eb6769c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C
InChI InChI=1S/C30H50/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h15-18,23-24H,9-14,19-22H2,1-8H3
InChI Key YYGNTYWPHWGJRM-UHFFFAOYSA-N
Popularity 1,290 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H50
Molecular Weight 410.70 g/mol
Exact Mass 410.391251595 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 11.60
Atomic LogP (AlogP) 10.60
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

Top
DTXSID4064767
Super Squalene; trans-Squalene;AddaVax
CHEMBL3561564
YYGNTYWPHWGJRM-UHFFFAOYSA-N
AKOS025243731
NCGC00181323-02
PD014521
FT-0772415

2D Structure

Top
2D Structure of Super Squalene; trans-Squalene;AddaVax

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.7004 70.04%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9462 94.62%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9601 96.01%
P-glycoprotein inhibitior + 0.6611 66.11%
P-glycoprotein substrate - 0.9803 98.03%
CYP3A4 substrate - 0.6864 68.64%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9863 98.63%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation - 0.6040 60.40%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6962 69.62%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6624 66.24%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.8513 85.13%
Thyroid receptor binding + 0.5941 59.41%
Glucocorticoid receptor binding - 0.5536 55.36%
Aromatase binding - 0.5869 58.69%
PPAR gamma + 0.6486 64.86%
Honey bee toxicity - 0.8442 84.42%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9916 99.16%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.43% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.96% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.68% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.29% 91.11%

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.
Abrus precatorius
Achyrocline alata
Acritopappus prunifolius
Ageratina anisochroma
Amaranthus caudatus
Antidesma montanum var. montanum
Artocarpus heterophyllus
Aster koraiensis
Athrixia elata
Austroeupatorium chaparense
Azolla nilotica
Barringtonia asiatica
Bauhinia purpurea
Beilschmiedia tsangii
Bidens pilosa
Bidens rubifolia
Broussonetia papyrifera
Calea pilosa
Calea rotundifolia
Calea sickii
Callicarpa pilosissima
Cassinia subtropica
Cineraria parvifolia
Cinnamomum kotoense
Cinnamomum philippinense
Cinnamomum subavenium
Cleistanthus indochinensis
Clibadium armanii
Corymbia citriodora
Croton cortesianus
Cryptocarya chinensis
Dactylanthus taylorii
Derris reticulata
Diospyros discolor
Diospyros maritima
Disynaphia multicrenulata
Duhaldea cappa
Ekebergia capensis
Eremanthus brasiliensis
Erigeron philadelphicus
Erythrophleum fordii
Eucalyptus ovata
Ficus septica
Galeopsis bifida
Garcinia linii
Garcinia multiflora
Geigeria brevifolia
Gentiana arisanensis
Gentiana lutea
Greenmaniella resinosa
Gymnanthemum corymbosum
Helichrysum cymosum
Helichrysum nudifolium
Heliopsis longipes
Inula salsoloides
Kleinia galpinii
Lasiolaena morii
Liabum solidagineum
Ligularia fischeri
Lindera glauca
Litsea acutivena
Maackia amurensis
Melaleuca leucadendra
Mentha spicata
Mikania grazielae
Milleria quinqueflora
Mondia whitei
Moscharia pinnatifida
Neoboutonia mannii
Neomirandea angularis
Nicotiana tabacum
Nidorella podocephala
Osteospermum muricatum
Panzerina lanata
Phoradendron reichenbachianum
Piptolepis leptospermoides
Polemannia montana
Porophyllum angustissimum
Pseudognaphalium gaudichaudianum
Psiadia ceylanica
Pteris pulchra
Rhododendron formosanum
Rosa transmorrisonensis
Rubia yunnanensis
Rudbeckia mollis
Rutidosis murchisonii
Salacia chinensis
Salvia fruticosa
Schistostephium crataegifolium
Scutellaria discolor
Sideritis candicans
Smallanthus uvedalia
Solanum dulcamara
Solidago nemoralis
Stilpnopappus glomeratus
Tectona grandis
Tetradium glabrifolium
Teucrium heterophyllum
Trichilia claussenii
Turnera diffusa
Vachellia pennatula
Verbesina macrophylla
Vitex trifolia subsp. litoralis
Zanthoxylum ailanthoides

Cross-Links

Top
PubChem 1105
NPASS NPC115959
LOTUS LTS0193020
wikiData Q72508801