1-Phytene

Details

Top
Internal ID 63ac8f26-a0c6-42c5-80e6-61ae7aac3a2d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadec-1-ene
SMILES (Canonical) CC(C)CCCC(C)CCCC(C)CCCC(C)C=C
SMILES (Isomeric) CC(C)CCCC(C)CCCC(C)CCCC(C)C=C
InChI InChI=1S/C20H40/c1-7-18(4)12-9-14-20(6)16-10-15-19(5)13-8-11-17(2)3/h7,17-20H,1,8-16H2,2-6H3
InChI Key XQNRAQZFPXUCOT-UHFFFAOYSA-N
Popularity 88 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H40
Molecular Weight 280.50 g/mol
Exact Mass 280.313001276 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.50
Atomic LogP (AlogP) 7.25
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

Top
DTXSID70336166
XQNRAQZFPXUCOT-UHFFFAOYSA-N
3,7,11,15-tetramethylhexadecene

2D Structure

Top
2D Structure of 1-Phytene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 + 0.7389 73.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.3291 32.91%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.9608 96.08%
OATP1B3 inhibitior + 0.9350 93.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6685 66.85%
P-glycoprotein inhibitior - 0.8778 87.78%
P-glycoprotein substrate - 0.8679 86.79%
CYP3A4 substrate - 0.6341 63.41%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9772 97.72%
CYP2C9 inhibition - 0.9108 91.08%
CYP2C19 inhibition - 0.9161 91.61%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.6894 68.94%
CYP2C8 inhibition - 0.9797 97.97%
CYP inhibitory promiscuity - 0.8322 83.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5364 53.64%
Eye corrosion + 0.9506 95.06%
Eye irritation + 0.7895 78.95%
Skin irritation + 0.8555 85.55%
Skin corrosion - 0.9843 98.43%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5285 52.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.9455 94.55%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6322 63.22%
Acute Oral Toxicity (c) III 0.8755 87.55%
Estrogen receptor binding - 0.8546 85.46%
Androgen receptor binding - 0.9045 90.45%
Thyroid receptor binding + 0.6273 62.73%
Glucocorticoid receptor binding - 0.6118 61.18%
Aromatase binding - 0.6431 64.31%
PPAR gamma - 0.7069 70.69%
Honey bee toxicity - 0.9220 92.20%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9946 99.46%

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
CHEMBL1907 P15144 Aminopeptidase N 88.96% 93.31%
CHEMBL2581 P07339 Cathepsin D 88.34% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 87.47% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.50% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.83% 96.09%
CHEMBL2039 P27338 Monoamine oxidase B 82.44% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 80.13% 94.73%

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.
Sideritis soluta

Cross-Links

Top
PubChem 529408
LOTUS LTS0237873
wikiData Q82103080