(S)-(+)-2-butanol

Details

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Internal ID 644ba75f-f8f7-48ce-9a3f-61cef02ef00a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (2S)-butan-2-ol
SMILES (Canonical) CCC(C)O
SMILES (Isomeric) CC[C@H](C)O
InChI InChI=1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3/t4-/m0/s1
InChI Key BTANRVKWQNVYAZ-BYPYZUCNSA-N
Popularity 136 references in papers

Physical and Chemical Properties

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Molecular Formula C4H10O
Molecular Weight 74.12 g/mol
Exact Mass 74.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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4221-99-2
(2S)-butan-2-ol
(S)-Butan-2-ol
(S)-2-butanol
(s)-(+)-sec-butanol
(2S)-2-butanol
2-Butanol, (+)-
(S)-sec-butanol
UNII-69KXU5NDTO
2-Butanol, (2S)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (S)-(+)-2-butanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.6464 64.64%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4307 43.07%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9459 94.59%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9852 98.52%
CYP3A4 substrate - 0.8480 84.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6625 66.25%
CYP3A4 inhibition - 0.9670 96.70%
CYP2C9 inhibition - 0.9332 93.32%
CYP2C19 inhibition - 0.8283 82.83%
CYP2D6 inhibition - 0.9320 93.20%
CYP1A2 inhibition - 0.6803 68.03%
CYP2C8 inhibition - 0.9973 99.73%
CYP inhibitory promiscuity - 0.9343 93.43%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6889 68.89%
Eye corrosion + 0.7797 77.97%
Eye irritation + 0.9668 96.68%
Skin irritation + 0.5320 53.20%
Skin corrosion - 0.9639 96.39%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7780 77.80%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5822 58.22%
skin sensitisation + 0.6410 64.10%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8909 89.09%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6330 63.30%
Acute Oral Toxicity (c) III 0.8286 82.86%
Estrogen receptor binding - 0.9284 92.84%
Androgen receptor binding - 0.9261 92.61%
Thyroid receptor binding - 0.8282 82.82%
Glucocorticoid receptor binding - 0.9351 93.51%
Aromatase binding - 0.9211 92.11%
PPAR gamma - 0.9011 90.11%
Honey bee toxicity - 0.9822 98.22%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.9900 99.00%
Fish aquatic toxicity - 0.8672 86.72%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.64% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.72% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.35% 85.14%
CHEMBL2885 P07451 Carbonic anhydrase III 83.78% 87.45%

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 africana
Aloe ferox
Aloe spicata
Aloe vera
Arctium lappa
Cornus officinalis
Elsholtzia splendens
Zingiber officinale

Cross-Links

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PubChem 444683
NPASS NPC26329