(R)-butane-1,3-diol

Details

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Internal ID e25b6d8a-0700-4181-acad-1b6942241bcc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (3R)-butane-1,3-diol
SMILES (Canonical) CC(CCO)O
SMILES (Isomeric) C[C@H](CCO)O
InChI InChI=1S/C4H10O2/c1-4(6)2-3-5/h4-6H,2-3H2,1H3/t4-/m1/s1
InChI Key PUPZLCDOIYMWBV-SCSAIBSYSA-N
Popularity 40 references in papers

Physical and Chemical Properties

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Molecular Formula C4H10O2
Molecular Weight 90.12 g/mol
Exact Mass 90.068079557 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.25
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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6290-03-5
(R)-(-)-1,3-Butanediol
(3R)-butane-1,3-diol
1,3-Butanediol, (3R)-
(R)-(-)-Butane-1,3-diol
(R)-1,3-butanediol
(R)-(-)-1,3-Butylene Glycol
MFCD00064277
1,3-Butanediol, (R)-
BU4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (R)-butane-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9650 96.50%
Caco-2 + 0.5222 52.22%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4672 46.72%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9573 95.73%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9545 95.45%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9621 96.21%
CYP3A4 substrate - 0.7777 77.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7098 70.98%
CYP3A4 inhibition - 0.9135 91.35%
CYP2C9 inhibition - 0.9170 91.70%
CYP2C19 inhibition - 0.8806 88.06%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition - 0.5422 54.22%
CYP2C8 inhibition - 0.9987 99.87%
CYP inhibitory promiscuity - 0.9078 90.78%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.7553 75.53%
Eye corrosion + 0.6964 69.64%
Eye irritation + 0.9629 96.29%
Skin irritation + 0.6212 62.12%
Skin corrosion - 0.7974 79.74%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7195 71.95%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5511 55.11%
skin sensitisation - 0.8172 81.72%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9087 90.87%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4895 48.95%
Acute Oral Toxicity (c) IV 0.7380 73.80%
Estrogen receptor binding - 0.9260 92.60%
Androgen receptor binding - 0.9401 94.01%
Thyroid receptor binding - 0.8375 83.75%
Glucocorticoid receptor binding - 0.8979 89.79%
Aromatase binding - 0.9390 93.90%
PPAR gamma - 0.9302 93.02%
Honey bee toxicity - 0.9733 97.33%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.9538 95.38%

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 92.25% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 89.81% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.55% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.58% 97.25%

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
Conioselinum anthriscoides
Foeniculum vulgare
Ligusticum officinale
Litchi chinensis

Cross-Links

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PubChem 637497
NPASS NPC150219