1,5-Decadiyne

Details

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Internal ID b11be705-cfac-4c86-a1f3-98f905147d5e
Taxonomy Acetylides
IUPAC Name deca-1,5-diyne
SMILES (Canonical) CCCCC#CCCC#C
SMILES (Isomeric) CCCCC#CCCC#C
InChI InChI=1S/C10H14/c1-3-5-7-9-10-8-6-4-2/h1H,4-8H2,2H3
InChI Key IWIDILFDSIIOSB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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53963-03-4
deca-1,5-diyne
1,5-Decadiyne, AldrichCPR
DTXSID7068895
MFCD00041651
AKOS015836211
BS-22675
CS-0186304
D1724
FT-0703217
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,5-Decadiyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.9202 92.02%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.5036 50.36%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9137 91.37%
P-glycoprotein inhibitior - 0.9802 98.02%
P-glycoprotein substrate - 0.9248 92.48%
CYP3A4 substrate - 0.6565 65.65%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate - 0.7406 74.06%
CYP3A4 inhibition - 0.9752 97.52%
CYP2C9 inhibition - 0.8667 86.67%
CYP2C19 inhibition - 0.9180 91.80%
CYP2D6 inhibition - 0.9504 95.04%
CYP1A2 inhibition + 0.5267 52.67%
CYP2C8 inhibition - 0.9118 91.18%
CYP inhibitory promiscuity - 0.6889 68.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5785 57.85%
Eye corrosion + 0.9869 98.69%
Eye irritation + 0.9812 98.12%
Skin irritation + 0.8634 86.34%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6694 66.94%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6554 65.54%
skin sensitisation + 0.8934 89.34%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.7558 75.58%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7257 72.57%
Acute Oral Toxicity (c) III 0.6997 69.97%
Estrogen receptor binding - 0.9135 91.35%
Androgen receptor binding - 0.8520 85.20%
Thyroid receptor binding - 0.6694 66.94%
Glucocorticoid receptor binding - 0.9368 93.68%
Aromatase binding - 0.8632 86.32%
PPAR gamma - 0.7712 77.12%
Honey bee toxicity - 0.9827 98.27%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9772 97.72%

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
CHEMBL2039 P27338 Monoamine oxidase B 95.26% 92.51%
CHEMBL230 P35354 Cyclooxygenase-2 93.83% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 93.65% 90.17%
CHEMBL2581 P07339 Cathepsin D 89.67% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.25% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.66% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.55% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.44% 91.81%
CHEMBL1951 P21397 Monoamine oxidase A 81.18% 91.49%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 80.78% 95.00%

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.
Scutellaria barbata

Cross-Links

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PubChem 104660
NPASS NPC68150