Scorodonin

Details

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Internal ID 6b15a2cb-66fd-4e0b-a301-9a2b1c010561
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name
SMILES (Canonical) C(C=C=CC#CCCl)O
SMILES (Isomeric) C(C=C=CC#CCCl)O
InChI InChI=1S/C7H7ClO/c8-6-4-2-1-3-5-7-9/h1,5,9H,6-7H2
InChI Key BRBJAAXWYUMXBE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H7ClO
Molecular Weight 142.58 g/mol
Exact Mass 142.0185425 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.93
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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74660-77-8
2,3-Heptadien-5-yn-1-ol, 7-chloro-, (R)-
RefChem:181973
(R)-7-Chlorohepta-2,3-dien-5-yn-1-ol
7-chlorohepta-2,3-dien-5-yn-1-ol
starbld0007515
orb3024799
SCHEMBL31398430
DTXSID60996172
CHEBI:223567
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Scorodonin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 + 0.6043 60.43%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.4525 45.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9413 94.13%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9447 94.47%
CYP3A4 substrate - 0.6178 61.78%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8026 80.26%
CYP3A4 inhibition - 0.9275 92.75%
CYP2C9 inhibition - 0.8348 83.48%
CYP2C19 inhibition - 0.7040 70.40%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.5134 51.34%
CYP2C8 inhibition - 0.9040 90.40%
CYP inhibitory promiscuity - 0.8222 82.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.6150 61.50%
Carcinogenicity (trinary) Danger 0.7000 70.00%
Eye corrosion + 0.9809 98.09%
Eye irritation + 0.9184 91.84%
Skin irritation + 0.8615 86.15%
Skin corrosion + 0.9623 96.23%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6547 65.47%
Micronuclear - 0.9241 92.41%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.7016 70.16%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6362 63.62%
Acute Oral Toxicity (c) II 0.6433 64.33%
Estrogen receptor binding - 0.8167 81.67%
Androgen receptor binding - 0.8600 86.00%
Thyroid receptor binding - 0.7039 70.39%
Glucocorticoid receptor binding - 0.7506 75.06%
Aromatase binding - 0.6577 65.77%
PPAR gamma - 0.6317 63.17%
Honey bee toxicity - 0.7612 76.12%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6490 64.90%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.17% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 86.78% 95.93%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.17% 83.57%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.56% 89.34%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.56% 86.92%

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 189818
LOTUS LTS0070912
wikiData Q82987845