4-Methyl-3-penten-1-ol

Details

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Internal ID 940f1202-01ca-4328-a2f5-4e1bc6b853bc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 4-methylpent-3-en-1-ol
SMILES (Canonical) CC(=CCCO)C
SMILES (Isomeric) CC(=CCCO)C
InChI InChI=1S/C6H12O/c1-6(2)4-3-5-7/h4,7H,3,5H2,1-2H3
InChI Key FKKLUOCEIANSFL-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 100.16 g/mol
Exact Mass 100.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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4-Methyl-3-penten-1-ol
763-89-3
3-Penten-1-ol, 4-methyl-
4-methyl-3-pentenol
2-methyl-2-penten-5-ol
homoprenol
4-methyl-3-pentene-1-ol
4-methyl-pent-3-en-1-ol
SCHEMBL133427
DTXSID60227175
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methyl-3-penten-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8793 87.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.6687 66.87%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.9277 92.77%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9280 92.80%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.9840 98.40%
CYP3A4 substrate - 0.7572 75.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9270 92.70%
CYP2C9 inhibition - 0.9432 94.32%
CYP2C19 inhibition - 0.9103 91.03%
CYP2D6 inhibition - 0.9316 93.16%
CYP1A2 inhibition - 0.8426 84.26%
CYP2C8 inhibition - 0.9931 99.31%
CYP inhibitory promiscuity - 0.8848 88.48%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.7012 70.12%
Eye corrosion + 0.7328 73.28%
Eye irritation + 0.9922 99.22%
Skin irritation + 0.8866 88.66%
Skin corrosion + 0.5812 58.12%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7697 76.97%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5476 54.76%
skin sensitisation + 0.8370 83.70%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9368 93.68%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7231 72.31%
Acute Oral Toxicity (c) III 0.8346 83.46%
Estrogen receptor binding - 0.9472 94.72%
Androgen receptor binding - 0.9411 94.11%
Thyroid receptor binding - 0.9299 92.99%
Glucocorticoid receptor binding - 0.8836 88.36%
Aromatase binding - 0.9160 91.60%
PPAR gamma - 0.8413 84.13%
Honey bee toxicity - 0.9385 93.85%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.7594 75.94%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.06% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 83.04% 87.45%
CHEMBL2581 P07339 Cathepsin D 80.32% 98.95%

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.
Aloe arborescens
Capsicum annuum

Cross-Links

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PubChem 136582
NPASS NPC39743
LOTUS LTS0205648
wikiData Q83106854