Callyspongenol B

Details

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Internal ID 743e6fb0-e7f9-4e04-806e-ec68bfadd4b3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (4Z,19Z)-docosa-4,19-dien-2,9,11,21-tetrayn-1-ol
SMILES (Canonical) C#CC=CCCCCCCC#CC#CCCCC=CC#CCO
SMILES (Isomeric) C#C/C=C\CCCCCCC#CC#CCCC/C=C\C#CCO
InChI InChI=1S/C22H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h1,3-4,18-19,23H,5-10,15-17,22H2/b4-3-,19-18-
InChI Key QZOMSTWCVSLZGH-WLXZLGQWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H26O
Molecular Weight 306.40 g/mol
Exact Mass 306.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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CHEMBL468045
(4Z,19Z)-docosa-4,19-dien-2,9,11,21-tetrayn-1-ol

2D Structure

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2D Structure of Callyspongenol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9818 98.18%
Caco-2 - 0.5586 55.86%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.3624 36.24%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8472 84.72%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6510 65.10%
P-glycoprotein inhibitior - 0.7310 73.10%
P-glycoprotein substrate - 0.9028 90.28%
CYP3A4 substrate - 0.5384 53.84%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.7593 75.93%
CYP3A4 inhibition - 0.9384 93.84%
CYP2C9 inhibition - 0.8142 81.42%
CYP2C19 inhibition - 0.8741 87.41%
CYP2D6 inhibition - 0.9570 95.70%
CYP1A2 inhibition - 0.6590 65.90%
CYP2C8 inhibition - 0.7107 71.07%
CYP inhibitory promiscuity - 0.7247 72.47%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5631 56.31%
Eye corrosion + 0.9702 97.02%
Eye irritation - 0.7617 76.17%
Skin irritation + 0.7365 73.65%
Skin corrosion - 0.5955 59.55%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7282 72.82%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6485 64.85%
skin sensitisation + 0.7217 72.17%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.5589 55.89%
Acute Oral Toxicity (c) III 0.2946 29.46%
Estrogen receptor binding + 0.7690 76.90%
Androgen receptor binding + 0.5361 53.61%
Thyroid receptor binding + 0.6943 69.43%
Glucocorticoid receptor binding - 0.4683 46.83%
Aromatase binding + 0.6168 61.68%
PPAR gamma + 0.7786 77.86%
Honey bee toxicity - 0.8965 89.65%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5334 53.34%
Fish aquatic toxicity - 0.4294 42.94%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 91.03% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.89% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 83.74% 89.63%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 82.60% 92.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.52% 96.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.16% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 80.11% 97.00%

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.
Prunus persica

Cross-Links

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PubChem 10357825
LOTUS LTS0013466
wikiData Q105133705