3-Hydroxy-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione

Details

• Internal ID: aa81f1f2-4048-49da-9b5e-29bd7a93d953
• Taxonomy: Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
• IUPAC Name: 3-hydroxy-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione
• SMILES (Canonical): CC1(C(CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)C
• SMILES (Isomeric): CC1(C(CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)C
• InChI: InChI=1S/C15H14O4/c1-15(2)11(16)7-10-12(17)8-5-3-4-6-9(8)13(18)14(10)19-15/h3-6,11,16H,7H2,1-2H3
• InChI Key: ZWWVIPQQWSJFHS-UHFFFAOYSA-N
• Popularity: 1 reference in papers

Physical and Chemical Properties

• Molecular Formula: C₁₅H₁₄O₄
• Molecular Weight: 258.27 g/mol
• Exact Mass: 258.08920892 g/mol
• Topological Polar Surface Area (TPSA): 63.60 Ų
• XlogP: 1.70
• Atomic LogP (AlogP): 1.88
• H-Bond Acceptor: 4
• H-Bond Donor: 1
• Rotatable Bonds: 0

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9950	99.50%
Caco-2	+	0.4915	49.15%
Blood Brain Barrier	+	0.5500	55.00%
Human oral bioavailability	-	0.5000	50.00%
Subcellular localzation	Mitochondria	0.7502	75.02%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.9261	92.61%
OATP1B3 inhibitior	+	0.9811	98.11%
MATE1 inhibitior	-	0.8200	82.00%
OCT2 inhibitior	-	0.9500	95.00%
BSEP inhibitior	-	0.8763	87.63%
P-glycoprotein inhibitior	-	0.9429	94.29%
P-glycoprotein substrate	-	0.9317	93.17%
CYP3A4 substrate	+	0.5311	53.11%
CYP2C9 substrate	-	0.7958	79.58%
CYP2D6 substrate	-	0.7988	79.88%
CYP3A4 inhibition	-	0.5466	54.66%
CYP2C9 inhibition	+	0.5948	59.48%
CYP2C19 inhibition	+	0.5924	59.24%
CYP2D6 inhibition	+	0.5458	54.58%
CYP1A2 inhibition	+	0.5530	55.30%
CYP2C8 inhibition	-	0.9336	93.36%
CYP inhibitory promiscuity	-	0.7221	72.21%
UGT catelyzed	+	0.7000	70.00%
Carcinogenicity (binary)	-	0.9318	93.18%
Carcinogenicity (trinary)	Non-required	0.6202	62.02%
Eye corrosion	-	0.9877	98.77%
Eye irritation	+	0.5636	56.36%
Skin irritation	-	0.5767	57.67%
Skin corrosion	-	0.9015	90.15%
Ames mutagenesis	-	0.6600	66.00%
Human Ether-a-go-go-Related Gene inhibition	-	0.6845	68.45%
Micronuclear	-	0.5441	54.41%
Hepatotoxicity	-	0.5750	57.50%
skin sensitisation	-	0.6103	61.03%
Respiratory toxicity	+	0.7556	75.56%
Reproductive toxicity	+	0.9000	90.00%
Mitochondrial toxicity	+	0.7000	70.00%
Nephrotoxicity	+	0.4905	49.05%
Acute Oral Toxicity (c)	III	0.5957	59.57%
Estrogen receptor binding	+	0.8435	84.35%
Androgen receptor binding	+	0.6716	67.16%
Thyroid receptor binding	-	0.6268	62.68%
Glucocorticoid receptor binding	+	0.5398	53.98%
Aromatase binding	-	0.5952	59.52%
PPAR gamma	+	0.6633	66.33%
Honey bee toxicity	-	0.8598	85.98%
Biodegradation	-	0.6250	62.50%
Crustacea aquatic toxicity	+	0.5300	53.00%
Fish aquatic toxicity	+	0.9434	94.34%

Targets

Proven Targets:

No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL2581	P07339	Cathepsin D	97.12%	98.95%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	97.10%	95.56%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	92.08%	91.11%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	90.79%	99.23%
CHEMBL1806	P11388	DNA topoisomerase II alpha	90.32%	89.00%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	87.21%	96.09%
CHEMBL3401	O75469	Pregnane X receptor	87.15%	94.73%
CHEMBL1951	P21397	Monoamine oxidase A	85.06%	91.49%
CHEMBL3137262	O60341	LSD1/CoREST complex	84.39%	97.09%
CHEMBL4026	P40763	Signal transducer and activator of transcription 3	84.13%	82.69%
CHEMBL1994	P08235	Mineralocorticoid receptor	82.59%	100.00%
CHEMBL1293249	Q13887	Kruppel-like factor 5	82.31%	86.33%
CHEMBL3359	P21462	Formyl peptide receptor 1	80.30%	93.56%

Plants that contains it

• Rhinacanthus nasutus

Cross-Links

• PubChem: 11032562
• LOTUS: LTS0252067
• wikiData: Q105385275