Rotenone

Details

• Internal ID: f39a51b6-83a8-4659-a4eb-dfea7711f4f8
• Taxonomy: Phenylpropanoids and polyketides > Isoflavonoids > Rotenoids > Rotenones
• IUPAC Name: (1S,6R,13S)-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one
• SMILES (Canonical): CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC
• SMILES (Isomeric): CC(=C)[C@H]1CC2=C(O1)C=CC3=C2O[C@@H]4COC5=CC(=C(C=C5[C@@H]4C3=O)OC)OC
• InChI: InChI=1S/C23H22O6/c1-11(2)16-8-14-15(28-16)6-5-12-22(24)21-13-7-18(25-3)19(26-4)9-17(13)27-10-20(21)29-23(12)14/h5-7,9,16,20-21H,1,8,10H2,2-4H3/t16-,20-,21+/m1/s1
• InChI Key: JUVIOZPCNVVQFO-HBGVWJBISA-N
• Popularity: 12,292 references in papers

Physical and Chemical Properties

• Molecular Formula: C₂₃H₂₂O₆
• Molecular Weight: 394.40 g/mol
• Exact Mass: 394.14163842 g/mol
• Topological Polar Surface Area (TPSA): 63.20 Ų
• XlogP: 4.10
• Atomic LogP (AlogP): 3.70
• H-Bond Acceptor: 6
• H-Bond Donor: 0
• Rotatable Bonds: 3

Synonyms

• 83-79-4
• Dactinol
• Paraderil
• Barbasco
• Tubatoxin
• (-)-Rotenone
• (-)-cis-Rotenone
• Rotocide
• Derrin
• Derris
• Rotenon
• Nicouline
• Ronone
• Canex
• Deril
• Liquid Derris
• Cube-Pulver
• Dri-Kil
• Rotessenol
• Noxfire
• Rotefive
• Rotefour
• Rotenox
• Cubor
• Extrax
• Haiari
• Mexide
• Chem-Mite
• Cenol garden dust
• Curex flea duster
• Tubotoxin
• Gerane
• Prentox
• Ro-Ko
• Synpren
• Derris (insecticide)
• Pb-nox
• Rotenox 5EC
• 5'-beta-Rotenone
• Green Cross Warble Powder
• Nekoe
• Caswell No. 725
• Rotenone, dehydro
• Foliafume E.C.
• ENT 133
• Rotenona [Spanish]
• Rotenone, commercial
• CCRIS 895
• Rotacide
• Rotenona
• Rotenone [BSI:ISO]
• Protax
• HSDB 1762
• NCI-C55210
• 5'beta-Rotenone
• Rotacide E.C.
• EPA Pesticide Chemical Code 071003
• AI3-00133
• C23H22O6
• NSC26258
• EINECS 201-501-9
• NSC 26258
• Derris resins
• UNII-03L9OT429T
• MLS000738056
• CHEMBL429023
• 1,2,12,12a-Tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-(1)benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one
• DTXSID6021248
• CHEBI:28201
• 03L9OT429T
• Rotenone (ISO)
• CUBE
• NSC-26258
• (1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-2-alpha-isopropenyl-8,9-dimethoxy-
• (12aS,6aS,2R)-8,9-dimethoxy-2-(1-methylvinyl)-1,2-dihydrochromano[3,4-b]furano [2,3-h]chroman-6-one
• (2R,6aS,12aS)-8,9-dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrochromeno[3,4-b]furo[2,3-h]chromen-6(6aH)-one
• (2R-(2alpha,6aalpha,12aalpha))-1,2,12,12a-Tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)(1)benzopyrano(3,4-b)furo(2,3-h)benzopyran-6(6aH)-one
• 1,2,12,12aalpha-Tetrahydro-2a-isopropenyl-8,9-dimethoxy(1)benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one
• NCGC00017358-05
• ROTENONE [ISO]
• (1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, (2R-(2alpha,6aalpha,12aalpha))-
• (1S,6R,13S)-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one
• (2R,6aS,12aS)-1,2,12,12a-Tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one
• (2R,6aS,12aS)-1,2,6,6a,12,12a-hexahydro-2-isopropenyl-8,9-dimethoxychromeno(3,4-b)furo(2,3-h)chromen-6-one
• (2R-(6aalpha,12aalpha)-1,2-Dihydro-2-isopropenyl-8,9-dimethoxychromano(3,4-b)furo(2,3-h)chroman-6-on
• [2R-(2alpha,6aalpha,12aalpha)]-1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)[1]benzopyrano[3,4-b]furo[2,3-H][1]benzopyran-6(6aH)-one
• DTXCID901248
• Green cross warble
• 5'.beta.-Rotenone
• CAS-83-79-4
• (1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, (2R,6aS,12aS)-
• (2R,6aS,12aS)-1,2,6,6a,12,12a- hexahydro-2-isopropenyl-8,9- dimethoxychromeno[3,4-b] furo(2,3-h)chromen-6-one
• (2R,6aS,12aS)-1,2,6,6a,12,12a-hexahydro-2-isopropenyl-8,9-dimethoxychromeno[3,4-b]furo[2,3-h]chromen-6-one
• (2R,6aS,12aS)-2-isopropenyl-8,9-dimethoxy-1,2,12,12a-tetrahydrochromeno[3,4-b]furo[2,3-h]chromen-6(6aH)-one
• (2R,6aS,12aS)-8,9-Dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrofuro[2',3':7,8][1]benzopyrano[2,3-c][1]benzopyran-6(6aH)-one
• [1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, (2R,6aS,12aS)-
• SR-01000076110
• Foliafume
• Rotenoid
• Roteonone
• Nusyn
• :rotenone
• rote five
• WLN: T G5 D6 B666 CV HO MO POT&TT&J IY1&U1 SO1 TO1
• Foliafume E.C
• Rotacide E.C
• 5''beta-rotenone
• 5'b-Rotenone
• Rotocide E.C.
• (1)Benzopyrano[3,3-h](1)benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-2-.alpha.-iospropenyl-8,9-dimethoxy-
• [1]Benzopyrano[3,3-h][1]benzopyran-6(6a.alpha.H)-one, 1,2,12,12a.alpha.-tetrahydro-2.alpha.-isopropenyl-8,9-dimethoxy-
• [1]Benzopyrano[3,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, [2R-(2.alpha.,6a.alpha.,12a.alpha.)]-
• [1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, [2R-(2alpha,6aalpha,12aalpha)]-
• Derris, JMAF
• Prestwick_542
• Rotenone (7CI)
• rotenone (commercial)
• Rotenone, >=95%
• Spectrum_000065
• ROTENONE [HSDB]
• ROTENONE [MI]
• Spectrum2_000457
• Spectrum3_000158
• Spectrum4_001638
• Spectrum5_000455
• ROTENONE [MART.]
• D0F7CS
• Lopac0_001112
• SCHEMBL42253
• BSPBio_001896
• isopropenyl(dimethoxy)[?]one
• KBioGR_002075
• KBioSS_000465
• SPECTRUM200013
• DivK1c_000947
• ROTENONE [GREEN BOOK]
• SPBio_000534
• HMS502P09
• KBio1_000947
• KBio2_000465
• KBio2_003033
• KBio2_005601
• KBio3_001116
• inhibits NADH2 oxidation to NAD
• NSC8505
• JUVIOZPCNVVQFO-HBGVWJBISA-N
• NINDS_000947
• HMS3263O06
• BCP07278
• HY-B1756
• NSC-8505
• TNP00301
• Tox21_110819
• Tox21_201904
• Tox21_300695
• Tox21_501112
• BDBM50135527
• CCG-39886
• HB5398
• LMPK12060007
• AKOS004910398
• Tox21_110819_1
• CS-6067
• DB11457
• LP01112
• LS-1830
• SDCCGMLS-0066415.P001
• SDCCGSBI-0051081.P003
• IDI1_000947
• Rotenone 100 microg/mL in Acetonitrile
• NCGC00017358-01
• NCGC00017358-02
• NCGC00017358-03
• NCGC00017358-04
• NCGC00017358-06
• NCGC00017358-07
• NCGC00017358-08
• NCGC00017358-09
• NCGC00017358-10
• NCGC00017358-11
• NCGC00017358-14
• NCGC00017358-15
• NCGC00017358-22
• NCGC00094382-01
• NCGC00094382-02
• NCGC00094382-03
• NCGC00094382-04
• NCGC00094382-05
• NCGC00254603-01
• NCGC00259453-01
• NCGC00261797-01
• AC-31290
• AS-10183
• NCI60_002093
• SMR000393729
• EU-0101112
• R0090
• Rotenone, PESTANAL(R), analytical standard
• TRANSGENIC MODEL EVALUATION (ROTENONE)
• C07593
• R 8875
• 1,2,12,12a-Tetrahydro-8,9-dimethoxy-2-(1
• Q412388
• SR-01000076110-2
• SR-01000076110-5
• SR-01000076110-6
• W-104134
• BRD-K08316444-001-01-9
• BRD-K08316444-001-05-0
• ROTENONE (SEE ALSO TRANSGENICMODEL EVALUATION (ROTENONE))
• (2R,6a5,12axS)-1,2,12,12a-tetrahydro-2a-isopropenyl-8,9-dimethoxy(1)benzopyrano(3,4-b)furo(2,3-H)(1)benzopyran-6(6aH)-one
• (2R,6AS,12AS)-1,2,12,12A-TETRAHYDRO-8,9-DIMETHOXY-2-(1-METHYLETHENYL)(1)BENZOPYRANO(3,4-B)FURO(2,3-H)(1)BENZOPYRAN-6(6AH)-ONE
• (2R-(6aalpha,12aalpha)-1,2-Dihydro-2-isopropenyl-8,9-dimethoxychromano(3,4-b)furo(2,3-h)chroman-6-one
• [1] benzopirano [3,4-b] furo [2,3-h] [1] benzopirano-6 (6ah)-uno, 1,2,12,12 a-tetrahidro-8,9-dimetoxi-2-( 1-metiletenil)-, (2r, 6as, 12as)-
• [1]Benzopyrano[3,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-2-.alpha.-isopropenyl-8,9-dimethoxy-
• [1]Benzopyrano[3,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-2-isopropenyl-8,9-dimethoxy-
• [1]Benzopyrano[3,4-b]furo[ 2,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9- dimethoxy-2-(1-methylethenyl)-, [2R-(2?,6a?,12a?)]-
• [1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aalphaH)-one, 1,2,12,12aalpha-tetrahydro-2alpha-isopropenyl-8,9-dimethoxy- (8CI)
• [1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, (2R,6aS,12aS)- (9CI)
• [2R-(2alpha,6aalpha,12aalpha)]-1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-[1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-o ne
• [2R-(2alpha,6aalpha,12aalpha)]-1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-[1]Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one
• 1,2,12,12a-tetrahydro-2alpha-isopropenyl-8,9-dimethoxy(1)benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one
• 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-(1)benzopyrano(3,4-b)furo(2,3-h) (1)benzopyran-6(6aH)-one, (2R-(2alpha, 6alpha-12aalpha))-
• 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-(1)benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one, (2R-(2alpha, 6alpha-12aalpha))-
• 1,2,12,12A-TETRAHYDRO-8,9-DIMETHOXY-2-(1-METHYLETHENYL)-,[2R-(2.ALPHA.,6A.ALPHA.,12A.ALHA.)]-
• 1,2,12,12a-Tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one, 9CI
• 2-Isopropenyl-8,9-dimethoxy-1,2,12,12a-tetrahydrochromeno[3,4-b]furo[2,3-H]chromen-6(6ah)-one
• Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-on e, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, ([2.2.1]R-([2.2.1]alpha,6aalpha,[2.2.1][2.2.1]aalpha))-
• Benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one, 1,2,12,12a-tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-, ([2.2.1]R-([2.2.1]alpha,6aalpha,[2.2.1][2.2.1]aalpha))-
• Tubatoxin 1,2,12,12a,-Tetrahydro-8,9-dimethoxy-2-(1-methylethenyl)-[1]benzopyrano[3,4-b]furo[2,3-h][1]-benzopyran-6(6aH)-one

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9955	99.55%
Caco-2	+	0.6872	68.72%
Blood Brain Barrier	+	0.5500	55.00%
Human oral bioavailability	+	0.5429	54.29%
Subcellular localzation	Mitochondria	0.6885	68.85%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	-	0.7738	77.38%
OATP1B3 inhibitior	+	0.9599	95.99%
MATE1 inhibitior	-	0.9200	92.00%
OCT2 inhibitior	-	0.9500	95.00%
BSEP inhibitior	+	0.7962	79.62%
P-glycoprotein inhibitior	+	0.8551	85.51%
P-glycoprotein substrate	-	0.5225	52.25%
CYP3A4 substrate	+	0.6359	63.59%
CYP2C9 substrate	-	0.7859	78.59%
CYP2D6 substrate	-	0.7307	73.07%
CYP3A4 inhibition	+	0.7961	79.61%
CYP2C9 inhibition	-	0.7686	76.86%
CYP2C19 inhibition	+	0.8993	89.93%
CYP2D6 inhibition	-	0.9231	92.31%
CYP1A2 inhibition	+	0.9106	91.06%
CYP2C8 inhibition	+	0.4644	46.44%
CYP inhibitory promiscuity	+	0.8226	82.26%
UGT catelyzed	-	0.0000	0.00%
Carcinogenicity (binary)	-	0.9900	99.00%
Carcinogenicity (trinary)	Non-required	0.7166	71.66%
Eye corrosion	-	0.9843	98.43%
Eye irritation	+	0.7112	71.12%
Skin irritation	-	0.7739	77.39%
Skin corrosion	-	0.9622	96.22%
Ames mutagenesis	-	0.9200	92.00%
Human Ether-a-go-go-Related Gene inhibition	-	0.5214	52.14%
Micronuclear	+	0.5559	55.59%
Hepatotoxicity	+	0.6000	60.00%
skin sensitisation	-	0.5678	56.78%
Respiratory toxicity	-	0.7778	77.78%
Reproductive toxicity	+	0.9000	90.00%
Mitochondrial toxicity	-	0.8000	80.00%
Nephrotoxicity	+	0.6356	63.56%
Acute Oral Toxicity (c)	II	0.7236	72.36%
Estrogen receptor binding	+	0.8905	89.05%
Androgen receptor binding	+	0.6300	63.00%
Thyroid receptor binding	+	0.8461	84.61%
Glucocorticoid receptor binding	+	0.8413	84.13%
Aromatase binding	-	0.5765	57.65%
PPAR gamma	+	0.8708	87.08%
Honey bee toxicity	+	0.9768	97.68%
Biodegradation	-	0.8750	87.50%
Crustacea aquatic toxicity	+	0.7800	78.00%
Fish aquatic toxicity	+	0.9833	98.33%

Targets

Proven Targets:

CHEMBL ID	UniProt ID	Name	Min activity	Assay type	Source
CHEMBL3577	P00352	Aldehyde dehydrogenase 1A1	35481.3 nM	Potency	via CMAUP
CHEMBL1293236	P46063	ATP-dependent DNA helicase Q1	3162.3 nM	Potency	via CMAUP
CHEMBL1293237	P54132	Bloom syndrome protein	22387.2 nM; 22387.2 nM	Potency; Potency	via CMAUP; via CMAUP
CHEMBL3622	P33261	Cytochrome P450 2C19	3648.6 nM	IC50	via CMAUP
CHEMBL3397	P11712	Cytochrome P450 2C9	31622.8 nM	Potency	via CMAUP
CHEMBL340	P08684	Cytochrome P450 3A4	15848.9 nM; 15848.9 nM	Potency; Potency	via CMAUP; via CMAUP
CHEMBL2392	P06746	DNA polymerase beta	39810.7 nM	Potency	via CMAUP
CHEMBL1293278	O75496	Geminin	1412.5 nM	Potency	via CMAUP
CHEMBL4261	Q16665	Hypoxia-inducible factor 1 alpha	79.4 nM	Potency	via Super-PRED
CHEMBL1293226	B2RXH2	Lysine-specific demethylase 4D-like	39810.7 nM	Potency	via CMAUP
CHEMBL4040	P28482	MAP kinase ERK2	794.3 nM	Potency	via Super-PRED
CHEMBL1293224	P10636	Microtubule-associated protein tau	8912.5 nM	Potency	via CMAUP
CHEMBL4499	P03905	NADH-ubiquinone oxidoreductase chain 4	3.5 nM	IC50	DOI: 10.1016/S0960-894X(01)81204-X
CHEMBL5162	Q6W5P4	Neuropeptide S receptor	12589.3 nM	Potency	via CMAUP
CHEMBL1293298	Q01453	Peripheral myelin protein 22	47.8 nM; 47.8 nM	Potency; Potency	via CMAUP; via Super-PRED
CHEMBL1293235	P02545	Prelamin-A/C	501.2 nM; 501.2 nM; 891.3 nM	Potency; Potency; Potency	via Super-PRED; via CMAUP; via CMAUP
CHEMBL2842	P42345	Serine/threonine-protein kinase mTOR	46.5 nM; 46.5 nM; 58.5 nM	Potency; Potency; Potency	via Super-PRED; via CMAUP; via CMAUP
CHEMBL3371	P50406	Serotonin 6 (5-HT6) receptor	870 nM	IC50	via CMAUP
CHEMBL1293232	Q16637	Survival motor neuron protein	63.1 nM; 63.1 nM	Potency; Potency	via Super-PRED; via CMAUP
CHEMBL1293256	P40225	Thrombopoietin	31.6 nM	Potency	via Super-PRED
CHEMBL1963	P16473	Thyroid stimulating hormone receptor	1258.9 nM; 1258.9 nM; 794.3 nM	Potency; Potency; Potency	via CMAUP; via CMAUP; via Super-PRED
CHEMBL1075138	Q9NUW8	Tyrosyl-DNA phosphodiesterase 1	5 nM; 5 nM	Potency; Potency	via CMAUP; via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	96.23%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	96.18%	96.09%
CHEMBL2581	P07339	Cathepsin D	93.79%	98.95%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	90.49%	95.56%
CHEMBL1806	P11388	DNA topoisomerase II alpha	90.02%	89.00%
CHEMBL1293249	Q13887	Kruppel-like factor 5	89.99%	86.33%
CHEMBL4481	P35228	Nitric oxide synthase, inducible	89.57%	94.80%
CHEMBL5608	Q16288	NT-3 growth factor receptor	89.56%	95.89%
CHEMBL241	Q14432	Phosphodiesterase 3A	87.90%	92.94%
CHEMBL2535	P11166	Glucose transporter	87.80%	98.75%
CHEMBL5311	P37023	Serine/threonine-protein kinase receptor R3	85.28%	82.67%
CHEMBL1994	P08235	Mineralocorticoid receptor	84.01%	100.00%
CHEMBL4478	Q00975	Voltage-gated N-type calcium channel alpha-1B subunit	82.85%	97.14%
CHEMBL3713062	P10646	Tissue factor pathway inhibitor	81.67%	97.33%
CHEMBL3060	Q9Y345	Glycine transporter 2	81.49%	99.17%
CHEMBL5339	Q5NUL3	G-protein coupled receptor 120	80.22%	95.78%

Plants that contains it

• Achillea cretica
• Ageratina riparia
• Allium macrostemon
• Amorpha fruticosa
• Antheroporum pierrei
• Cordia americana
• Crotalaria paniculata
• Deguelia scandens
• Derris brevipes
• Derris elliptica
• Derris trifoliata
• Erycibe expansa
• Geijera parviflora
• Glycosmis lanceolata
• Indigofera spicata
• Isodon rubescens
• Lonchocarpus salvadorensis
• Millettia ferruginea
• Millettia pachycarpa
• Millettia pachyloba
• Mundulea chapelieri
• Neorautanenia mitis
• Pachyrhizus erosus
• Pachyrhizus tuberosus
• Patrinia scabra
• Pedicularis semitorta
• Piscidia piscipula
• Scopolia japonica
• Spatholobus parviflorus
• Spiraea japonica
• Tephrosia leiocarpa
• Tephrosia linearis
• Tephrosia macropoda
• Tephrosia purpurea
• Tephrosia strigosa
• Tephrosia villosa
• Tephrosia vogelii

Cross-Links

• PubChem: 6758
• NPASS: NPC298093
• ChEMBL: CHEMBL429023
• LOTUS: LTS0257248
• wikiData: Q412388