(2S,3S,4E,6E,10Z,13Z,16Z,19Z,22Z,26E,28S,29S)-2,29-diaminotriaconta-4,6,10,13,16,19,22,26-octaene-3,28-diol

Details

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Internal ID 38f2ad9f-6f3b-43df-902c-4e1e2152e3fc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (2S,3S,4E,6E,10Z,13Z,16Z,19Z,22Z,26E,28S,29S)-2,29-diaminotriaconta-4,6,10,13,16,19,22,26-octaene-3,28-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48N2O2/c1-27(31)29(33)25-23-21-19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22-24-26-30(34)28(2)32/h3,5-6,8-9,11-12,14-15,17,20,22-30,33-34H,4,7,10,13,16,18-19,21,31-32H2,1-2H3/b5-3-,8-6-,11-9-,14-12-,17-15-,22-20+,25-23+,26-24+/t27-,28-,29-,30-/m0/s1
InChI Key WVXXLSBPRGHRHS-MADRGNLTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48N2O2
Molecular Weight 468.70 g/mol
Exact Mass 468.37157878 g/mol
Topological Polar Surface Area (TPSA) 92.50 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,4E,6E,10Z,13Z,16Z,19Z,22Z,26E,28S,29S)-2,29-diaminotriaconta-4,6,10,13,16,19,22,26-octaene-3,28-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9630 96.30%
Caco-2 - 0.7848 78.48%
Blood Brain Barrier + 0.6065 60.65%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4910 49.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8444 84.44%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9554 95.54%
P-glycoprotein inhibitior + 0.6637 66.37%
P-glycoprotein substrate - 0.9003 90.03%
CYP3A4 substrate - 0.6662 66.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3787 37.87%
CYP3A4 inhibition - 0.8450 84.50%
CYP2C9 inhibition - 0.8940 89.40%
CYP2C19 inhibition - 0.9046 90.46%
CYP2D6 inhibition - 0.8874 88.74%
CYP1A2 inhibition - 0.8175 81.75%
CYP2C8 inhibition - 0.9578 95.78%
CYP inhibitory promiscuity - 0.8388 83.88%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.5844 58.44%
Eye corrosion - 0.7214 72.14%
Eye irritation - 0.9394 93.94%
Skin irritation - 0.6507 65.07%
Skin corrosion - 0.5710 57.10%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8003 80.03%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6199 61.99%
skin sensitisation - 0.7603 76.03%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.6752 67.52%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7206 72.06%
Acute Oral Toxicity (c) III 0.7653 76.53%
Estrogen receptor binding + 0.7515 75.15%
Androgen receptor binding - 0.8192 81.92%
Thyroid receptor binding + 0.5938 59.38%
Glucocorticoid receptor binding + 0.6449 64.49%
Aromatase binding + 0.5511 55.11%
PPAR gamma + 0.6309 63.09%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.7493 74.93%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.93% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.05% 85.14%
CHEMBL2581 P07339 Cathepsin D 90.79% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.11% 90.24%
CHEMBL2885 P07451 Carbonic anhydrase III 83.00% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.92% 99.17%

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 163194696
LOTUS LTS0152486
wikiData Q105313860