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CandActCFTR used public reference

The following publication reference has been reported to contain CFTR related structural information.
"K McKenzie" "E Kwon" "PL Zeitlin" "M Lim" "AD Floyd"


Below you will find all the structures identified in the publication. Be warned that this does not imply any activity. n=5

ID: 1
InChIKey: TZBJGXHYKVUXJN-UHFFFAOYSA-N
SMILES: C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O

biological descriptors:

CFTR relevance: CFTR corrector

Category:
Influence on CFTR function enhances CFTR function
Order of interaction unknown
subcellular compartment several

chemical graph of compound 1



CID is 5280961
synonyms found at PubChem are:
genistein, 446-72-0, Prunetol, Genisteol, 4',5,7-Trihydroxyisoflavone, Genisterin, Sophoricol, 5,7,4'-Trihydroxyisoflavone, 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one, Bonistein, Genestein, Differenol A, NPI 031L, 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-, 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one, C.I. 75610, SIPI 807-1, 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one, UNII-DH2M523P0H, NSC 36586, 4,5,7-Trihydroxyiso-flavone, Lactoferrin-genistein, CCRIS 7675, 4',5, 7-Trihydroxyisoflavone, 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone, NSC36586, CHEMBL44, EINECS 207-174-9, IN1327, BRN 0263823, PTI G4660 (Genistein), ISOFLAVONE, 4',5,7-TRIHYDROXY-, MLS000738127, DH2M523P0H, STO514, CHEBI:28088, PTI-G4660, SIPI-9764-I, TZBJGXHYKVUXJN-UHFFFAOYSA-N, 4′,5,7-Trihydroxyisoflavone, TNP00151, NSC-36586, GENISTEIN (ENDOCRINE DISRUPTER), GEN, NCGC00015479-09, DSSTox_CID_2308, G 6649, G10000, DSSTox_RID_76542, DSSTox_GSID_22308, ENDOCRINE DISRUPTOR (GENISTEIN) (SEE ALSO GENISTEIN (446-72-0)), CAS-446-72-0, SR-01000075498, HSDB 7475, PTI G4660, 3kgt, 3kgu, 4&prime, Genistein, 8, Genistein,(S), PTI-G 4660, Genistein (flavonoid), PubChem9852, Spectrum_000320, Tocris-1110, 1x7r, 2qa8, Genistein 85% HPLC, SpecPlus_000305, AC1NQXT4, Spectrum2_000638, Spectrum3_000678, Spectrum4_001543, Spectrum5_000106, Lopac-G-6649, 4',7-Trihydroxyisoflavone, D0L4FS, MolMap_000022, UPCMLD-DP096, 4,5,7-Trihydroxyisoflavone, 4,6,7-Trihydroxyisoflavone, Isoflavone,5,7-trihydroxy-, Lopac0_000520, Oprea1_224620, Oprea1_437815, SCHEMBL19166, BSPBio_002375, KBioGR_002006, KBioGR_002564, KBioSS_000800, KBioSS_002573, SPECTRUM210296, 5-18-04-00594 (Beilstein Handbook Reference), BIDD:ER0113, DivK1c_006401, Genistein, analytical standard, SPBio_000636, 4',5,7-Trihydroxy isoflavone, 4',5,7-trihydroxy-Isoflavone, GTPL2826, MEGxp0_000568, 4,5,7-Trihydroxy Iso-Flavone, DTXSID5022308, UPCMLD-DP096:001, ACon1_001065, BDBM19459, cid_5280961, KBio1_001345, KBio2_000800, KBio2_002564, KBio2_003368, KBio2_005132, KBio2_005936, KBio2_007700, KBio3_001595, KBio3_003042, AOB5073, CHEBI: 28088, cMAP_000086, MolPort-000-003-911, Bio1_000445, Bio1_000934, Bio1_001423, HMS2271K09, HMS3261H21, HMS3267K14, HMS3428M01, HMS3649B22, HMS3654D17, ACT05962, ALBB-015886, BCP07581, KS-00000MH8, Prunetol solution, 20 mM in DMSO, Tox21_110161, Tox21_201428, Tox21_300585, Tox21_500520, AC-472, BBL010484, CCG-38551, CG-009, Genistein solution, 20 mM in DMSO, LMPK12050218, MFCD00016952, s1342, SBB066115, STK801619, ZINC18825330, AKOS001590147, Tox21_110161_1, CS-1534, DB01645, KS-5128, LP00520, LS-1266, MCULE-4857649752, RL03694, RP29616, SMP1_000133, Genistein; 4',5,7-Trihydroxyisoflavone, NCGC00015479-01, NCGC00015479-02, NCGC00015479-04, NCGC00015479-05, NCGC00015479-06, NCGC00015479-07, NCGC00015479-08, NCGC00015479-10, NCGC00015479-11, NCGC00015479-12, NCGC00015479-13, NCGC00015479-14, NCGC00015479-15, NCGC00015479-16, NCGC00015479-17, NCGC00015479-18, NCGC00015479-19, NCGC00015479-20, NCGC00025005-01, NCGC00025005-02, NCGC00025005-03, NCGC00025005-04, NCGC00025005-05, NCGC00025005-06, NCGC00025005-07, NCGC00169711-01, NCGC00169711-02, NCGC00254275-01, NCGC00258979-01, NCGC00261205-01, 690224-00-1, AJ-70669, AN-15821, BC200563, HY-14596, KB-52241, NCI60_003369, SC-04581, SMR000112580, ST056352, AB1004490, EU-0100520, FT-0603395, G0272, N1861, Genistein, disposable screening library format, 46G720, C06563, G-2535, Genistein, synthetic, >=98% (HPLC), powder, J10015, K00046, S-7751, US8552057, 2, AB00052696_09, AB00052696_12, A826657, Genistein, primary pharmaceutical reference standard, I06-0431, Q-100484, SR-01000075498-1, SR-01000075498-3, SR-01000075498-6, 3-(4-hydroxyphenyl)-5,7-bis(oxidanyl)chromen-4-one, 4 inverted exclamation marka,5,7-Trihydroxyisoflavone, BRD-K43797669-001-02-3, BRD-K43797669-001-03-1, BRD-K43797669-001-10-6, Genistein, from Glycine max (soybean), ~98% (HPLC), SR-01000075498-10, 5,7-dihydroxy-3-(4-hydroxyphenyl)-1-benzopyran-4-one, F0001-2388, 4H-1-Benzopyran-4-one,7-dihydroxy-3-(4-hydroxyphenyl)-, UNII-71B37NR06D component TZBJGXHYKVUXJN-UHFFFAOYSA-N, Genistein, United States Pharmacopeia (USP) Reference Standard, Genistein, Pharmaceutical Secondary Standard; Certified Reference Material, 4 inverted exclamation marka,5,7-Trihydroxyisoflavone; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

ID: 41
InChIKey: IYRMWMYZSQPJKC-UHFFFAOYSA-N
SMILES: C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O

biological descriptors:

CFTR relevance: influence of intracellular CFTR distribution

Category:
Influence on CFTR function enhances CFTR function
Order of interaction indirect
subcellular compartment ER & Golgi (Translation, quality control, trafficking, PTM)

chemical graph of compound 41



CID is 5280863
synonyms found at PubChem are:
kaempferol, 520-18-3, Kempferol, Kaempherol, Populnetin, Rhamnolutein, Robigenin, Trifolitin, Pelargidenolon, Rhamnolutin, Swartziol, 3,4',5,7-Tetrahydroxyflavone, Indigo Yellow, Kampherol, Campherol, Kampferol, Nimbecetin, Kaemferol, 5,7,4'-Trihydroxyflavonol, 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one, Pelargidenolon 1497, 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one, C.I. 75640, CCRIS 41, NSC 407289, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one, 4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-, Flavone, 3,4',5,7-tetrahydroxy-, NSC 656277, UNII-731P2LE49E, EINECS 208-287-6, CHEMBL150, BRN 0304401, AI3-36096, CHEBI:28499, IYRMWMYZSQPJKC-UHFFFAOYSA-N, 731P2LE49E, 3,4′,5,7-Tetrahydroxyflavone, NSC656277, NSC-407289, NSC-656277, CAS-520-18-3, DSSTox_CID_768, DSSTox_RID_75781, DSSTox_GSID_20768, Q-100584, SMR000112585, Pelargidenon, Kampcetin, 3,5,7,4'-Tetrahydroxyflavone, HSDB 7703, 4det, Kaempferol,(S), AC1NQXP1, 5,4'-Trihydroxyflavonol, Prestwick0_001098, Prestwick1_001098, Prestwick2_001098, Prestwick3_001098, D0G3TK, 3,5,7-Tetrahydroxyflavone, 4',5,7-trihydroxyflavonol, BIDD:PXR0073, Oprea1_650954, SCHEMBL18817, BSPBio_001176, 5-18-05-00251 (Beilstein Handbook Reference), MLS000697730, MLS001055391, MLS001074884, MLS006010737, BIDD:ER0134, SPBio_003058, 3,4,5,7-Tetrahydroxyflavone, Kaempferol, analytical standard, BDBM7462, BPBio1_001294, MEGxp0_001283, DTXSID7020768, Flavone,4',5,7-tetrahydroxy-, ACon1_001867, cid_5280863, CHEBI: 28499, MolPort-001-741-568, HMS1571K18, HMS2098K18, HMS2267I09, HMS3656M03, KAEMPFEROL ROBIGENIN; 3,4',5,7-TETRAHYDRO-XY-FLAVONE, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1- benzopyran-4-one, Kaempferol, >=97.0% (HPLC), TNP00039, ZINC3869768, Tox21_201165, Tox21_303363, AC-544, CK0011, GP7425, HSCI1_000027, LMPK12110003, LS-176, MFCD00016938, NSC407289, s2314, SBB066091, Kaempferol solution, 20 mM in DMSO, AKOS015895240, Kaempferol, >=90% (HPLC), powder, CCG-202823, CS-1273, DB01852, GS-3570, MCULE-8965218413, NCGC00016480-01, NCGC00016480-02, NCGC00016480-03, NCGC00016480-04, NCGC00016480-05, NCGC00016480-06, NCGC00016480-07, NCGC00016480-09, NCGC00091036-01, NCGC00091036-02, NCGC00164322-01, NCGC00179275-01, NCGC00179275-02, NCGC00257464-01, NCGC00258717-01, AN-15750, BC215517, CC-29746, HY-14590, KB-79581, SC-17291, ST030560, AB0010534, TR-018501, AB00514046, FT-0614420, K0018, N1719, W1682, 3,4',5,7-tetrahydroxy-Flavone (7CI,8CI), C05903, J10449, Kaempferol, disposable screening library format, S00111, W-2776, Flavone, 3,4',5,7-tetrahydroxy- (7CI,8CI), 520K183, A828886, C-18018, SR-01000765646, I06-0240, Kaempferol, primary pharmaceutical reference standard, SR-01000765646-3, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-chromen-4-one, BRD-K12807006-001-05-2, BRD-K12807006-001-10-2, 2-(4-hydroxyphenyl)-3,5,7-tris(oxidanyl)chromen-4-one, 3,4',5,7-tetrahydroxyflavone solution, 20 mM in DMSO, A91A6666-86C8-4B33-B3EF-F74CD3CD7F47, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-1-benzopyran-4-one, 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one #, 3,5,7-Trihydroxy-2-[4-hydroxy-phenyl]-4H-1-benzopyran-4-one, 4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-(4-hydroxyphenyl)-, 4H-1-Benzopyran-4-one,5,7-trihydroxy-2-(4-hydroxyphenyl)-, Kaempferol, United States Pharmacopeia (USP) Reference Standard, 3,5,7-Trihydroxy-2-[4-hydroxy- phenyl]-4H-1-benzopyran-4-one, 4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)- (9CI), 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one solution, 20 mM in DMSO, 4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol

ID: 9
InChIKey: KZNIFHPLKGYRTM-UHFFFAOYSA-N
SMILES: C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O

biological descriptors:

CFTR relevance: inactive

Category:
Influence on CFTR function inconsistent assignment
Order of interaction unknown
subcellular compartment ER & Golgi (Translation, quality control, trafficking, PTM)

chemical graph of compound 9



CID is 5280443
synonyms found at PubChem are:
apigenin, 520-36-5, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one, Chamomile, Spigenin, Versulin, Apigenol, 4',5,7-Trihydroxyflavone, Apigenine, C.I. Natural Yellow 1, 5,7,4'-Trihydroxyflavone, Pelargidenon 1449, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone, 2-(p-Hydroxyphenyl)-5,7-dihydroxychromone, UCCF 031, NSC 83244, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one, UNII-7V515PI7F6, 5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one, CCRIS 3789, CHEBI:18388, CHEMBL28, EINECS 208-292-3, 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-, BRN 0262620, FLAVONE, 4',5,7-TRIHYDROXY-, 4′,5,7-Trihydroxyflavone, KZNIFHPLKGYRTM-UHFFFAOYSA-N, 7V515PI7F6, NSC83244, NSC-83244, CAS-520-36-5, ST056301, DSSTox_CID_2391, DSSTox_RID_76568, DSSTox_GSID_22391, Q-100586, Q-200822, SMR000326850, SR-01000075663, Chamomile Powder, HSDB 7573, 4der, 4dgm, 4hkk, Naringenin, 18, Prestwick_719, Apigenin, 13, PubChem9831, Tocris-1227, 3cf9, 4',7-Trihydroxyflavone, BiomolKI_000078, Prestwick0_000414, Prestwick1_000414, Prestwick2_000414, Prestwick3_000414, Spectrum2_000428, Spectrum3_001882, Spectrum4_001999, Lopac-A-3145, BiomolKI2_000082, D00RIX, 4,5, 7-Trihydroxyflavone, AC1NQX15, Lopac0_000065, Oprea1_622293, SCHEMBL19428, 4',5,7-trihydroxy-Flavone, Apigenin, analytical standard, BSPBio_000368, BSPBio_003384, KBioGR_002565, SPECTRUM200846, 5-18-04-00574 (Beilstein Handbook Reference), MLS000697626, MLS000859991, MLS001074874, MLS006011839, BIDD:ER0135, DivK1c_000798, SCHEMBL222227, SPBio_000416, SPBio_002307, ghl.PD_Mitscher_leg0.1194, BDBM7458, BPBio1_000406, GTPL4136, MEGxp0_000176, DTXSID6022391, ACon1_002450, cid_5280443, HMS502H20, KBio1_000798, KBio3_002887, BIK9018, OR7265T, MolPort-001-740-354, NINDS_000798, ZX-AFC000435, Bio1_000376, Bio1_000865, Bio1_001354, HMS1569C10, HMS1922P22, HMS2096C10, HMS2230D17, HMS3260M11, HMS3267D21, HMS3373B18, HMS3561P09, HMS3655D18, Apigenin, >=95.0% (HPLC), 4',5,7-Trihydroxyflavone, 97%, ACN-S003241, BCP28288, HY-N1201, ZINC3871576, ZX-AT019281, Tox21_201542, Tox21_302884, Tox21_500065, Apigenin; 4',5,7-Trihydroxyflavone, BBL010499, BS0030, CCG-40061, GP1532, HSCI1_000221, LMPK12110005, MFCD00006831, s2262, SBB066087, STK801630, AKOS002140699, AC-8011, ACN-034762, AN-8432, CS-5432, DB07352, EBD2138579, LP00065, LS-2209, MCULE-6141069907, ND-9076, SDCCGMLS-0066379.P001, TRA0067512, IDI1_000798, SMP2_000338, Apigenin, >=97% (TLC), from citrus, NCGC00015049-01, NCGC00015049-02, NCGC00015049-03, NCGC00015049-04, NCGC00015049-05, NCGC00015049-06, NCGC00015049-07, NCGC00015049-08, NCGC00015049-09, NCGC00015049-10, NCGC00015049-11, NCGC00015049-12, NCGC00015049-13, NCGC00015049-14, NCGC00015049-15, NCGC00015049-16, NCGC00015049-18, NCGC00025057-01, NCGC00025057-02, NCGC00025057-03, NCGC00025057-04, NCGC00025057-05, NCGC00025057-06, NCGC00025057-07, NCGC00025057-08, NCGC00025057-09, NCGC00169835-01, NCGC00169835-02, NCGC00169835-03, NCGC00256419-01, NCGC00259092-01, NCGC00260750-01, 4CN-0925, AJ-46351, AK-88794, CC-24158, CJ-10995, KB-78227, NCI60_041830, SC-05011, SY005957, TS-00897, AB0010536, AB1011450, AX8015784, LY 080400, ST2411642, TC-307820, TR-018510, EU-0100065, FT-0622445, FT-0623582, N1828, 20A365, A 3145, C01477, J10341, K00045, M-6923, Apigenin, >=97% (TLC), from parsley, powder, Biochem Biophys Res Comm 212: 767 (1997), 4 inverted exclamation marka,5,7-Trihydroxyflavone, 5,7-dihydroxy-2-(4-hydroxyphenyl)-chromen-4-one, Apigenin, primary pharmaceutical reference standard, C-16977, 4 inverted exclamation mark ,5,7-trihydroxyflavone, I06-0221, SR-01000075663-1, SR-01000075663-3, SR-01000075663-7, SR-01000075663-8, BRD-K01493881-001-10-4, BRD-K01493881-001-17-9, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one #, 4H-1-Benzopyran-4-one,7-dihydroxy-2-(4-hydroxyphenyl)-, D50A2D8A-6D8B-4708-B21E-2DE9580D033F, Apigenin, United States Pharmacopeia (USP) Reference Standard, 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)- (9CI), 461015-54-3, 8002-66-2

ID: 18
InChIKey: REFJWTPEDVJJIY-UHFFFAOYSA-N
SMILES: C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O

biological descriptors:

CFTR relevance: CFTR activator

Category:
Influence on CFTR function enhances CFTR function
Order of interaction unknown
subcellular compartment unknown

chemical graph of compound 18



CID is 5280343
synonyms found at PubChem are:
quercetin, 117-39-5, Meletin, Sophoretin, Quercetine, Xanthaurine, Quercetol, Quercitin, Quertine, 3,3',4',5,7-Pentahydroxyflavone, 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one, Flavin meletin, Cyanidelonon 1522, T-Gelb bzw. grun 1, 3,5,7,3',4'-Pentahydroxyflavone, C.I. Natural Yellow 10, Quercetin content, Kvercetin, Quertin, C.I. Natural red 1, Kvercetin [Czech], Natural Yellow 10, C.I. 75670, CI Natural Yellow 10, 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one, 3',4',5,7-Tetrahydroxyflavan-3-ol, 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, C.I. Natural yellow 10 & 13, CCRIS 1639, HSDB 3529, Flavone, 3,3',4',5,7-pentahydroxy-, NCI-C60106, UNII-9IKM0I5T1E, NSC 9219, 3',4',5,7-tetrahydroxyflavon-3-ol, 3,5,7-Trihydroxy-2-(3,4-dihydroxyphenyl)-4H-chromen-4-on, Cyanidenolon 1522, CHEBI:16243, AI3-26018, NSC9219, CHEMBL50, EINECS 204-187-1, MixCom3_000183, BRN 0317313, C.I . natural yellow 10, 9IKM0I5T1E, CI 75670, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chromen-4-one, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one, 2-(3,4-Dihydroxy-phenyl)-3,5,7-trihydroxy-chromen-4-one, REFJWTPEDVJJIY-UHFFFAOYSA-N, KUC104418N, KUC107684N, 3,3',4,5,7-Pentahydroxyflavone, LIM-5662, LNS-5662, NSC-9219, TNP00070, TNP00089, KSC-23-76, KSC-10-126, P0042, DSSTox_CID_1218, Q 0125, DSSTox_RID_76017, DSSTox_GSID_21218, 74893-81-5, QUE, CU-01000012502-3, Q-200333, BRD9794, 3,5,7-trihydroxy-2-(3,4-dihydroxyphenyl)-4H-chromen-4-one, BRD-9794, CAS-117-39-5, NSC57655, NSC58588, SR-01000076098, Ritacetin, Quer, 4dfu, 4mra, Quercetin_sathishkumar, Quercetin (Sophoretin), Quercetin - Sophoretin, Spectrum_000124, Tocris-1125, 3cf8, AC1NQWX8, BiomolKI_000062, 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, zirconium(2+) salt (1:1), Maybridge1_008992, Prestwick0_000507, Prestwick1_000507, Prestwick2_000507, Prestwick3_000507, Spectrum2_000059, Spectrum3_000642, Spectrum4_000807, Spectrum5_001389, Lopac-Q-0125, C.I. natural yellow 13, BiomolKI2_000068, D0K8KX, Enicostemma Littorale Blume, UPCMLD-DP081, NCIOpen2_007628, NCIOpen2_007882, BIDD:PXR0007, Lopac0_000999, SCHEMBL19723, BSPBio_000433, BSPBio_001068, BSPBio_002243, KBioGR_000408, KBioGR_001293, KBioSS_000408, KBioSS_000584, 5-18-05-00494 (Beilstein Handbook Reference), KSC497C4F, MLS006011766, BIDD:ER0315, DivK1c_000485, SCHEMBL219729, SPECTRUM1500672, SPBio_000217, SPBio_002354, AC1Q795S, AC1Q795T, BDBM7460, BPBio1_000477, GTPL5346, MEGxp0_000381, SGCUT00001, 3,4',5,7-Pentahydroxyflavone, DTXSID4021218, UPCMLD-DP081:001, ACon1_000560, CTK3J7142, HMS501I07, KBio1_000485, KBio2_000408, KBio2_000584, KBio2_002976, KBio2_003152, KBio2_005544, KBio2_005720, KBio3_000775, KBio3_000776, KBio3_001463, 3,7,3',4'-Pentahydroxyflavone, MolPort-001-740-557, NINDS_000485, 3',5,7-Tetrahydroxyflavan-3-ol, Bio1_000369, Bio1_000858, Bio1_001347, Bio2_000374, Bio2_000854, HMS1362F09, HMS1792F09, HMS1923O19, HMS1990F09, HMS3263G19, HMS3267M12, HMS3649D04, HMS3656C15, to_000078, ZINC3869685, 3,5,7,3',4'-Pentahydroxyflavon, Tox21_202308, Tox21_300285, Tox21_500999, ANW-73134, BBL005513, BS0155, CCG-40054, CQ0011, Flavone,3',4',5,7-pentahydroxy-, GP9232, LMPK12110004, LS-589, MFCD00006828, NSC324608, Quercetin solution, 20 mM in DMSO, s2391, SBB012521, STK365650, Quercetin, >=95% (HPLC), solid, 3,4',5,5',7-pentahydroxy-Flavone, AKOS000511724, CS-3981, DB04216, DS-3416, EBD2197934, LP00999, MCULE-2433372790, NUT0000107, RTX-012622, IDI1_000485, IDI1_002129, KS-0000021G, SMP1_000252, Flavone, 3,4',5,5',7-pentahydroxy-, NCGC00015870-01, NCGC00015870-02, NCGC00015870-03, NCGC00015870-05, NCGC00015870-06, NCGC00015870-07, NCGC00015870-08, NCGC00015870-09, NCGC00015870-10, NCGC00015870-11, NCGC00015870-12, NCGC00015870-13, NCGC00015870-14, NCGC00015870-15, NCGC00015870-16, NCGC00015870-17, NCGC00015870-18, NCGC00015870-19, NCGC00015870-21, NCGC00015870-22, NCGC00015870-23, NCGC00015870-24, NCGC00025016-01, NCGC00025016-02, NCGC00025016-03, NCGC00025016-04, NCGC00025016-05, NCGC00025016-06, NCGC00025016-07, NCGC00025016-08, NCGC00168962-01, NCGC00168962-02, NCGC00168962-03, NCGC00168962-04, NCGC00254218-01, NCGC00259857-01, NCGC00261684-01, 4CN-0923, AC-19596, AC-29756, AJ-46321, AK106169, AN-22768, BAS 00649429, CJ-10980, HY-18085, KB-66753, LS-69030, NCI60_042036, S295, SC-25667, SMR000112559, ST024706, ST057237, Quercetin, Sophoretin, Meletin, Quercetine, AX8030401, KB-221421, EU-0100999, FT-0603318, FT-0655108, N1841, Q0025, ST24039236, Quercetin, disposable screening library format, Quercetin; 3,3',4',5,7-Pentahydroxyflavone, 17Q395, A-8821, C00389, K00029, S00057, WLN: T66 BO EVJ CR CQ DQ & DQ GQ IQ, SR-01000076098-1, SR-01000076098-3, SR-01000076098-7, SR-01000076098-8, BRD-K97399794-001-02-1, BRD-K97399794-001-07-0, BRD-K97399794-001-09-6, BRD-K97399794-001-11-2, BRD-K97399794-335-03-1, SR-01000076098-11, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chromone;hydrate, 3,3',4',5,7-pentahydroxyflavone solution, 20 mM in DMSO, A1784/0075599, 49643640-FD4C-4B93-BD28-0D7C2021CC52, 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one #, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one solution, 20 mM in DMSO, 73123-10-1

ID: 10
InChIKey: OBKXEAXTFZPCHS-UHFFFAOYSA-M
SMILES: C1=CC=C(C=C1)CCCC(=O)[O-]

biological descriptors:

CFTR relevance: little or no effect

Category:
Influence on CFTR function likely enhances CFTR function
Order of interaction unknown
subcellular compartment unknown

chemical graph of compound 10



CID is 22053264
synonyms found at PubChem are:
4-phenylbutanoate, 4-Phenylbutyric acid anion, BDBM36184, CHEBI:75317, OBKXEAXTFZPCHS-UHFFFAOYSA-M, AKOS024437455, CJ-00370, ZB001717, J3.540.463E, AB01275463-01, AB01275463_02, A812651