(Z)-Santalol

Details

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Internal ID 0fb2f534-f688-4915-9c74-08d3a0cb7085
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (7Z,9Z,11Z,13Z)-pentadeca-7,9,11,13-tetraen-1-ol
SMILES (Canonical) CC=CC=CC=CC=CCCCCCCO
SMILES (Isomeric) C/C=C\C=C/C=C\C=C/CCCCCCO
InChI InChI=1S/C15H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-9,16H,10-15H2,1H3/b3-2-,5-4-,7-6-,9-8-
InChI Key RAPKQMZFSCMPDF-FUKINOADSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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RAPKQMZFSCMPDF-FUKINOADSA-N

2D Structure

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2D Structure of (Z)-Santalol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.8763 87.63%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4644 46.44%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.8404 84.04%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5163 51.63%
P-glycoprotein inhibitior - 0.9352 93.52%
P-glycoprotein substrate - 0.9461 94.61%
CYP3A4 substrate - 0.6336 63.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.9444 94.44%
CYP2C9 inhibition - 0.8913 89.13%
CYP2C19 inhibition - 0.9372 93.72%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.7041 70.41%
CYP2C8 inhibition - 0.9295 92.95%
CYP inhibitory promiscuity - 0.8878 88.78%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6829 68.29%
Eye corrosion + 0.9068 90.68%
Eye irritation + 0.8671 86.71%
Skin irritation + 0.7764 77.64%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8099 80.99%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5353 53.53%
skin sensitisation + 0.8252 82.52%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5311 53.11%
Acute Oral Toxicity (c) III 0.8549 85.49%
Estrogen receptor binding - 0.4753 47.53%
Androgen receptor binding + 0.5200 52.00%
Thyroid receptor binding - 0.4920 49.20%
Glucocorticoid receptor binding - 0.4873 48.73%
Aromatase binding + 0.6642 66.42%
PPAR gamma + 0.5919 59.19%
Honey bee toxicity - 0.9726 97.26%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6749 67.49%
Fish aquatic toxicity - 0.6781 67.81%

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
CHEMBL2885 P07451 Carbonic anhydrase III 90.52% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.52% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.46% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.69% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.66% 91.11%
CHEMBL2581 P07339 Cathepsin D 81.10% 98.95%

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.
Santalum album
Wurfbainia longiligularis
Wurfbainia villosa
Wurfbainia villosa var. xanthioides

Cross-Links

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PubChem 91753183
NPASS NPC43635