Clathculin A

Details

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Internal ID 4d0e01d8-e667-45c0-b4ee-7e53589bc8df
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Tertiary amines > Trialkylamines
IUPAC Name N'-[(12Z)-heptadeca-12,16-dien-10-ynyl]-N,N'-dimethylethane-1,2-diamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H38N2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23(3)21-19-22-2/h4,7-8,22H,1,5-6,11-21H2,2-3H3/b8-7-
InChI Key PRWVCICUUGWJMV-FPLPWBNLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H38N2
Molecular Weight 318.50 g/mol
Exact Mass 318.303499221 g/mol
Topological Polar Surface Area (TPSA) 15.30 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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N'-[(12Z)-heptadeca-12,16-dien-10-ynyl]-N,N'-dimethylethane-1,2-diamine

2D Structure

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2D Structure of Clathculin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8339 83.39%
Caco-2 + 0.5921 59.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.9202 92.02%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8610 86.10%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5832 58.32%
P-glycoprotein inhibitior - 0.7635 76.35%
P-glycoprotein substrate - 0.5826 58.26%
CYP3A4 substrate + 0.6489 64.89%
CYP2C9 substrate + 0.5914 59.14%
CYP2D6 substrate + 0.4554 45.54%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9120 91.20%
CYP2C19 inhibition - 0.9063 90.63%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7566 75.66%
CYP2C8 inhibition - 0.8833 88.33%
CYP inhibitory promiscuity - 0.9671 96.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6101 61.01%
Eye corrosion + 0.7694 76.94%
Eye irritation - 0.9010 90.10%
Skin irritation + 0.6387 63.87%
Skin corrosion + 0.9068 90.68%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6798 67.98%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6197 61.97%
skin sensitisation - 0.6585 65.85%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.8449 84.49%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.4890 48.90%
Acute Oral Toxicity (c) III 0.7905 79.05%
Estrogen receptor binding - 0.4755 47.55%
Androgen receptor binding - 0.8346 83.46%
Thyroid receptor binding + 0.7696 76.96%
Glucocorticoid receptor binding - 0.6313 63.13%
Aromatase binding + 0.5802 58.02%
PPAR gamma + 0.5340 53.40%
Honey bee toxicity - 0.6243 62.43%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8117 81.17%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.86% 95.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.70% 96.09%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 92.61% 85.40%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.44% 99.17%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.58% 91.79%
CHEMBL321 P14780 Matrix metalloproteinase 9 89.74% 92.12%
CHEMBL202 P00374 Dihydrofolate reductase 89.50% 89.92%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.31% 89.34%
CHEMBL5524 Q99873 Protein-arginine N-methyltransferase 1 88.16% 96.67%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 87.98% 97.34%
CHEMBL2581 P07339 Cathepsin D 87.67% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 87.47% 83.82%
CHEMBL2916 O14746 Telomerase reverse transcriptase 87.26% 90.00%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 85.85% 91.67%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.79% 92.86%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 83.55% 81.58%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.47% 91.11%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.35% 95.83%
CHEMBL222 P23975 Norepinephrine transporter 83.01% 96.06%
CHEMBL1275221 Q96LA8 Protein arginine N-methyltransferase 6 82.88% 98.33%
CHEMBL2885 P07451 Carbonic anhydrase III 82.70% 87.45%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.94% 91.03%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.78% 96.38%
CHEMBL1829 O15379 Histone deacetylase 3 81.69% 95.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.91% 97.79%
CHEMBL3401 O75469 Pregnane X receptor 80.67% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10519632
LOTUS LTS0222299
wikiData Q105213960