Arbutin: mechanism of its depigmenting action in human melanocyte culture

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de Oliveira, K. B., Palú, É., Weffort‐Santos, A. M., & de Oliveira, B. H. (2012) · Revista Brasileira de Farmacognosia · doi:10.1590/s0102-695x2012005000135 · Cited by 33

A Novel Melanin Inhibitor: Hydroperoxy Traxastane-Type Triterpene from Flowers of Arnica montana

Maeda, K., Naitou, T., Umishio, K., Fukuhara, T., & Motoyama, A. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.873 · Cited by 33

Inhibition of Tyrosinase by Protocatechuic Aldehyde

No, J. K., Kim, M. S., Kim, Y. J., Bae, S.-J., Choi, J. S., & Chung, H. Y. (2004) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x04001801 · Cited by 33

Discrimination between Alternative Substrates and Inhibitors of Tyrosinase

Ortiz‐Ruiz, C. V., García‐Molina, M. D. M., Tudela, J., Tomas-Martinez, V., & Garcı́a-Cánovas, F. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf5051816 · Cited by 33

α-Viniferin Improves Facial Hyperpigmentation via Accelerating Feedback Termination of cAMP/PKA-Signaled Phosphorylation Circuit in Facultative Melanogenesis

Yun, C., Ko, S. M., Choi, Y. P., Kim, B. J., Lee, J., Kim, J. M., Kim, J. Y., Song, J. Y., Kim, S.-H., Hwang, B. Y., et al. (2018) · Theranostics · doi:10.7150/thno.24385 · Cited by 32

Lavender and peppermint essential oils as effective mushroom tyrosinase inhibitors: a basic study

Fiocco, D., Fiorentino, D., Frabboni, L., Benvenuti, S., Orlandini, G., Pellati, F., & Gallone, A. (2011) · Flavour and Fragrance Journal · doi:10.1002/ffj.2072 · Cited by 32

Rosmarinic acid and arbutin suppress osteoclast differentiation by inhibiting superoxide and NFATc1 downregulation in RAW 264.7 cells

Omori, A., Yoshimura, Y., Deyama, Y., & Suzuki, K. (2015) · Biomedical Reports · doi:10.3892/br.2015.452 · Cited by 31

Ethnopharmacological importance and medical applications of Myrothamnus flabellifolius Welw. (Myrothamnaceae)-A review

Erhabor, J. O., Komakech, R., Kang, Y., Tang, M., & Matsabisa, M. G. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.112576 · Cited by 31

Determination of tyrosinase-cyanidin-3-O-glucoside and (−/+)-catechin binding modes reveal mechanistic differences in tyrosinase inhibition

Lee, K. E., Bharadwaj, S., Sahoo, A. K., Yadava, U., & Kang, S. G. (2021) · Scientific Reports · doi:10.1038/s41598-021-03569-1 · Cited by 31

Manassantin A inhibits cAMP‐induced melanin production by down‐regulating the gene expressions of MITF and tyrosinase in melanocytes

Lee, H. D., Lee, W., Roh, E., Seo, C., Son, J., Lee, S. H., Hwang, B. Y., Jung, S., Han, S., & Kim, Y. S. (2011) · Experimental Dermatology · doi:10.1111/j.1600-0625.2011.01296.x · Cited by 31

Inhibitory Effects of 2-Amino-3H-phenoxazin-3-one on the Melanogenesis of Murine B16 Melanoma Cell Line

MIYAKE, M., Yamamoto, S., Osamu, S. A. N. O., Fujii, M., Kohno, K., Ushio, S., Iwaki, K., & Fukuda, S. (2010) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.90795 · Cited by 31

Luteolin 7-Sulfate Attenuates Melanin Synthesis through Inhibition of CREB- and MITF-Mediated Tyrosinase Expression

Lee, S. W., Kim, J. H., Song, H., Seok, J. K., Hong, S. S., & Boo, Y. C. (2019) · Antioxidants · doi:10.3390/antiox8040087 · Cited by 31

Inhibition of Melanogenesis by Selina-4(14),7(11)-dien-8-one Isolated from Atractylodis Rhizoma Alba

Chang, Y., Kim, C., MinHwan, J., Lim, Y., Lee, S.-H., & Kang, S. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.719 · Cited by 30

Enzymatic Synthesis and Characterization of Hydroquinone Galactoside UsingKluyveromyces lactisLactase

Kim, G., Lee, J. H., Jung, S.-H., Seo, E.-S., Jin, S.-D., Kim, G. J., Cha, J., Kim, E.-J., Park, K.-D., & Kim, D. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf101748j · Cited by 30

Activation of MITF by Argan Oil Leads to the Inhibition of the Tyrosinase and Dopachrome Tautomerase Expressions in B16 Murine Melanoma Cells

Villareal, M. O., Kume, S., Bourhim, T., Bakhtaoui, F. Z., Kashiwagi, K., Han, J., Gadhi, C., & Isoda, H. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/340107 · Cited by 31

Resorcinol alkyl glucosides as potent tyrosinase inhibitors

Ishioka, W., Oonuki, S., Iwadate, T., & Nihei, K. (2018) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2018.11.029 · Cited by 30

Pigmentary disorders in ethnic skin

Halder, R. M., Nandedkar, M. A., & NEAL, K. W. (2003) · Dermatologic Clinics · doi:10.1016/s0733-8635(03)00083-4 · Cited by 30

Anti-melanogenic effects of resveratryl triglycolate, a novel hybrid compound derived by esterification of resveratrol with glycolic acid

Park, S., Seok, J. K., Kwak, J. Y., Choi, Y., Hong, S. S., Suh, H., Park, W., & Boo, Y. C. (2016) · Archives of Dermatological Research · doi:10.1007/s00403-016-1644-9 · Cited by 28

Bond-based 2D TOMOCOMD-CARDD approach for drug discovery: aiding decision-making in ‘in silico’ selection of new lead tyrosinase inhibitors

Marrero‐Ponce, Y., Khan, M. T. H., Casañola‐Martín, G. M., Ather, A., Sultankhodzhaev, M. N., García‐Domenech, R., Torrens, F., & Rotondo, R. (2007) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-006-9094-7 · Cited by 28

Anti-melanogenic effects of δ-tocotrienol are associated with tyrosinase-related proteins and MAPK signaling pathway in B16 melanoma cells

Ng, L., Lin, L., Chen, C.-L., Chen, H.-W., Wu, S.-J., & Lin, C. (2014) · Phytomedicine · doi:10.1016/j.phymed.2014.03.003 · Cited by 28

4‐n‐butylresorcinol enhances proteolytic degradation of tyrosinase in B16F10 melanoma cells

Lee, S.-J., Son, Y. H., Lee, K. B., Lee, J., Kim, H. ‐., Jeong, E. M., Park, S. C., & Kim, I. (2016) · International Journal of Cosmetic Science · doi:10.1111/ics.12368 · Cited by 28

Nuclear Entry of CRTC1 as Druggable Target of Acquired Pigmentary Disorder

Yun, C., Hong, S. D., Lee, Y. H., Lee, J., Jung, D.-E., Kim, G. H., Kim, S., Jung, J., Kim, K., Lee, H., et al. (2019) · Theranostics · doi:10.7150/thno.30276 · Cited by 28

The correlation of in vitro mushroom tyrosinase activity with cellular tyrosinase activity and melanin formation in melanoma cells A2058

Song, T., Chen, C., Yang, N.-C., Fu, C., Chang, Y., & Chen, C.-L. (2020) · Journal of Food and Drug Analysis · doi:10.38212/2224-6614.2607 · Cited by 28

Pharmacological Aspects of a Bioactive Compound Arbutin: A Comprehensive Review

(2022) · Biointerface Research in Applied Chemistry · doi:10.33263/briac132.119 · Cited by 27

Synthesis of gold nanoparticles with glycosides: synthetic trends based on the structures of glycones and aglycones

Jung, J., Park, S., Hong, S., Ha, M. W., Park, H., Park, Y., Lee, H., & Park, Y. (2013) · Carbohydrate Research · doi:10.1016/j.carres.2013.12.012 · Cited by 27

Synthesis, characteristics and biological activity of pentacoordinated spirophosphoranes derived from amino acids

YU, L. ‐., Liu, Z., Fang, H., Zeng, Q., & Zhao, Y. (2005) · Amino Acids · doi:10.1007/s00726-005-0207-8 · Cited by 27

cAMP ‐dependent activation of protein kinase A as a therapeutic target of skin hyperpigmentation by diphenylmethylene hydrazinecarbothioamide

Shin, H., Hong, S. D., Roh, E., Jung, S., Cho, W., Park, S. H., Yoon, D. Y., Ko, S. M., Hwang, B. Y., Hong, J. T., et al. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13134 · Cited by 26

Human skin‐depigmenting effects of resveratryl triglycolate, a hybrid compound of resveratrol and glycolic acid

Jo, D. J., Seok, J. K., Kim, S. Y., Park, W., Baek, J. H., Kim, Y. M., & Boo, Y. C. (2018) · International Journal of Cosmetic Science · doi:10.1111/ics.12458 · Cited by 26

Ketonethiosemicarbazones: Structure–activity relationships for their melanogenesis inhibition

Pillaiyar, T., LEE, K. ‐., Sharma, V. K., Roh, E., Kim, Y. S., & Jung, S. (2011) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2011.04.146 · Cited by 26

Potential sources for the management global health problems and oxidative stress: Stachys byzantina and S. iberica subsp. iberica var. densipilosa

Sarıkürkçü, C., Kocak, M. S., Uren, M. C., Calapoğlu, M., & Tepe, A. S. (2016) · European Journal of Integrative Medicine · doi:10.1016/j.eujim.2016.04.010 · Cited by 26

SAR and QSAR research on tyrosinase inhibitors using machine learning methods

Wu, Y., Huo, D., Chen, G., & Yan, A. (2021) · SAR and QSAR in environmental research · doi:10.1080/1062936x.2020.1862297 · Cited by 28

The Organogermanium Compound THGP Suppresses Melanin Synthesis via Complex Formation with L-DOPA on Mushroom Tyrosinase and in B16 4A5 Melanoma Cells

Azumi, J., Takeda, T., Shimada, Y., Aso, H., & Nakamura, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194785 · Cited by 25

Acetoside inhibits α-MSH-induced melanin production in B16 melanoma cells by inactivation of adenyl cyclase

Song, H. S., & Sim, S. S. (2009) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.61.10.0011 · Cited by 25

Evidence that geniposide abrogates norepinephrine-induced hypopigmentation by the activation of GLP-1R-dependent c-kit receptor signaling in melanocyte

Wen-Jun, L., Hai-Yan, W., Wei, L., Ke-Yu, W., & Rui-Ming, W. (2008) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2008.03.021 · Cited by 25

Multiple uses of Essential Oil and By-Products from Various Parts of the Yakushima Native Cedar ( Cryptomeria Japonica )

Nakagawa, T., Zhu, Q., Ishikawa, H., Ohnuki, K., Kakino, K., Horiuchi, N., Shinotsuka, H., Naito, T., Matsumoto, T., Minamisawa, N., et al. (2015) · Journal of Wood Chemistry and Technology · doi:10.1080/02773813.2015.1057648 · Cited by 25

Arbutin promotes MC3T3‑E1 mouse osteoblast precursor cell proliferation and differentiation via the Wnt/β‑catenin signaling pathway

Man, X., Yang, L., Liu, S., Yang, L., Li, M., & Fu, Q. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10125 · Cited by 24

In vitro evaluation of patch formulations for topical delivery of gentisic acid in rats

Bian, S., Doh, H.-J., Zheng, J., Kim, J. S., Lee, C.-H., & Kim, D. (2003) · European Journal of Pharmaceutical Sciences · doi:10.1016/s0928-0987(02)00255-5 · Cited by 24

Soyasaponin Ag inhibits α-MSH-induced melanogenesis in B16F10 melanoma cells via the downregulation of TRP-2

Yang, S. H., Tsatsakis, A. M., Tzanakakis, G. N., Kim, H., Le, B., Sifaki, M., Spandidos, D. A., Tsukamoto, C., Golokhvast, K. S., Izotov, B. N., et al. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3061 · Cited by 24

Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on mushroom tyrosinase

Tokiwa, Y., Kitagawa, M., & Raku, T. (2006) · Biotechnology Letters · doi:10.1007/s10529-006-9267-4 · Cited by 24

In situ paper-based 3D cell culture for rapid screening of the anti-melanogenic activity

Pupinyo, N., Chatatikun, M., Chiabchalard, A., & Laiwattanapaisal, W. (2018) · The Analyst · doi:10.1039/c8an01725e · Cited by 24

Dual Inhibition of γ-Oryzanol on Cellular Melanogenesis: Inhibition of Tyrosinase Activity and Reduction of Melanogenic Gene Expression by a Protein Kinase A-Dependent Mechanism

Jun, H., Lee, J. H., Cho, B.-R., Seo, W. D., Kang, H.-W., Kim, D.-W., Cho, K.-J., & Lee, S. (2012) · Journal of Natural Products · doi:10.1021/np300250m · Cited by 23

FermentedViola mandshuricaInhibits Melanogenesis in B16 Melanoma Cells

Kwack, Y.-J., Kim, K.-S., Kim, K.-M., Hai Yang, Y. U., Chung, E., Kim, S.-J., Jae-Young, C. H. A., Lee, Y., & Lee, J. (2011) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.100641 · Cited by 23

Estimation of skin concentrations of topically applied lidocaine at each depth profile

Oshizaka, T., Kikuchi, K., Kadhum, W. R., Todo, H., Hatanaka, T., Wierzba, K., & Sugibayashi, K. (2014) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2014.08.046 · Cited by 23

Design, synthesis, and antimelanogenic effects of (2-substituted phenyl-1,3-dithiolan-4-yl)methanol derivatives

Kim, D. H., Kim, S. J., Ullah, S., Yun, H. Y., Chun, P., & Moon, H. R. (2017) · Drug Design Development and Therapy · doi:10.2147/dddt.s131538 · Cited by 23

Effects of matsutake mushroom scent compounds on tyrosinase and murine B16-F10 melanoma cells

Satooka, H., Cerda, P., Kim, H.-J., Wood, W. F., & Kubo, I. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.04.137 · Cited by 23

Identification of small peptides and glycinamide that inhibit melanin synthesis using a positional scanning synthetic peptide combinatorial library

Kim, J. H., Seok, J. K., Kim, Y. M., & Boo, Y. C. (2019) · British Journal of Dermatology · doi:10.1111/bjd.17634 · Cited by 23

Antioxidant, Anti-Inflammatory, and Anti-Aging Potential of a Kalmia angustifolia Extract and Identification of Some Major Compounds

Grenier, A., Legault, J., Pichette, A., Jean, L., Bélanger, A., & Pouliot, R. (2021) · Antioxidants · doi:10.3390/antiox10091373 · Cited by 24

Effects of cuminaldehyde on melanoma cells

Nitoda, T., Fan, M. D., & Kubo, I. (2008) · Phytotherapy Research · doi:10.1002/ptr.2374 · Cited by 23

Micellar liquid chromatographic determination of arbutin and hydroquinone in medicinal plant extracts and commercial cosmetic products

Thogchai, W., & Liawruangrath, B. (2013) · International Journal of Cosmetic Science · doi:10.1111/ics.12037 · Cited by 22

Evaluation of antityrosinase activity and mechanism, antioxidation, and UV filter properties of theaflavin

Chen, J., Ran, M., Wang, M., Liu, X., Liu, S., Ruan, Z., & Jin, N. G. (2021) · Biotechnology and Applied Biochemistry · doi:10.1002/bab.2166 · Cited by 22

Timeline of the Development of Skin-Lightening Active Ingredients in Japan

Maeda, K. (2022) · Molecules · doi:10.3390/molecules27154774 · Cited by 22

Chemical synthesis and tyrosinase-inhibitory activity of isotachioside and its related glycosides

Matsumoto, T., Nakajima, T., Iwadate, T., & Nihei, K. (2018) · Carbohydrate Research · doi:10.1016/j.carres.2018.06.004 · Cited by 22

Synthesis and Biological Evaluation of the Anti-Melanogenesis Effect of Coumaric and Caffeic Acid-Conjugated Peptides in Human Melanocytes

Park, K., & Kim, J. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00922 · Cited by 22

Physicochemical Characters of a Tyrosinase Inhibitor Produced by Streptomyces roseolilacinus NBRC 12815

Nakashima, T., Anzai, K., Kuwahara, N., Komaki, H., Miyadoh, S., Harayama, S., Tianero, M. D. B., Tanaka, J., Kanamoto, A., & Ando, K. (2009) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.32.832 · Cited by 22

Tyrosinase Inhibitory Activity of Ethanol Extracts from Medicinal and Edible Plants Cultivated in Okinawa and Identification of a Water-Soluble Inhibitor from the Leaves ofNandina domestica

Masuda, T., FUJITA, N., Odaka, Y., Takeda, Y., Yonemori, S., Nakamoto, K., & Kuninaga, H. (2007) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.70249 · Cited by 22

The Melanin Synthesis inhibition and Radical Scavenging Activities of Compounds Isolated from the Aerial Part of Lespedeza cyrtobotrya

Lee, C. (2010) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.0905.05054 · Cited by 22

Study of the characteristic fragmentation behavior of hydroquinone glycosides by electrospray ionization tandem mass spectrometry with optimization of collision energy

Liu, Y., He, J., Zhang, R., Shi, J., & Abliz, Z. (2009) · Journal of Mass Spectrometry · doi:10.1002/jms.1593 · Cited by 22

An electrochemical sensor based on a clay-coated screen-printed electrode for the determination of arbutin

Shih, Y., & Zen, J. (2000) · Analytica Chimica Acta · doi:10.1016/s0003-2670(00)00725-x · Cited by 22

Melanogenesis regulatory activity of the ethyl acetate fraction from Arctium lappa L. leaf on α-MSH–induced B16/F10 melanoma cells

Lee, C. J., Park, S. K., Kang, J. Y., Kim, J. M., Yoo, S. K., Han, H. J., Kim, D., & Heo, H. J. (2019) · Industrial Crops and Products · doi:10.1016/j.indcrop.2019.111581 · Cited by 21

Valorization of biomass polyphenols as potential tyrosinase inhibitors

Pham, T., Cazier, E. A., Gormally, E., & Lawrence, P. (2023) · Drug Discovery Today · doi:10.1016/j.drudis.2023.103843 · Cited by 22

Biotransformation of 4‐Hydroxybenzen Derivatives by Hairy Root Cultures of Polygonum multiflorum Thunb.

Yan, C., Yu, R., Zhang, Z., & Kong, L. (2007) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00400.x · Cited by 21

Hypopigmentary Effects of EthylP‐Methoxycinnamate Isolated fromKaempferia galanga

Ko, H., Kim, H. J., Kim, S. Y., Yun, H., Baek, K. J., Kwon, N. S., Whang, W. K., Choi, H., Park, K., & Kim, D. (2013) · Phytotherapy Research · doi:10.1002/ptr.4995 · Cited by 21

In vitro anti-melanogenic effects of chimeric compounds, 2-(substituted benzylidene)-1,3-indanedione derivatives with a β-phenyl-α, β -unsaturated dicarbonyl scaffold

Ryu, I. Y., Choi, I., Jung, H. J., Ullah, S., Choi, H.-J., Al-Amin, M., Chun, P., & Moon, H. R. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.104688 · Cited by 21

Zeolite 4A, a Synthetic Silicate, Suppresses Melanogenesis through the Degradation of Microphthalmia-Associated Transcription Factor by Extracellular Signal-Regulated Kinase Activation in B16F10 Melanoma Cells

Shin, Y. J., Han, C., Lee, C. S., Kim, H.-S., Ko, S., Hwang, S. K., Ko, S., Shin, J. W., Ye, S., & Chung, M. (2010) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.33.72 · Cited by 21

Inhibitory Mechanism of Melanin Synthesis by Glutathione

Matsuki, M., Watanabe, T., Ogasawara, A., MIKAMI, T., & Matsumoto, T. (2008) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.128.1203 · Cited by 21

Nano-vesicular systems for melanocytes targeting and melasma treatment: In-vitro characterization, ex-vivo skin retention, and preliminary clinical appraisal

Hatem, S., Kamel, A. O., Elkheshen, S. A., Nasr, M., Moftah, N. H., Ragai, M. H., Hoffy, N. M. E., & Elezaby, R. S. (2024) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2024.124731 · Cited by 20

Human Tyrosinase Inhibitor in Rum Distillate Wastewater

Takara, K., Iwasaki, H., Ujihara, K., & Wada, K. (2008) · Journal of Oleo Science · doi:10.5650/jos.57.191 · Cited by 20

Evaluation of antioxidant and anti-melanogenic activities of different extracts from aerial parts of Nepeta binaludensis Jamzad in murine melanoma B16F10 cells.

Tayarani‐Najaran, Z., Akaberi, M., Vatani, M., & Emami, S. A. (2016) · Europe PMC (PubMed Central) · Cited by 20

6-Benzylaminopurine stimulates melanogenesis via cAMP-independent activation of protein kinase A

Kim, S., Lee, J., Jung, E., Lee, J., Huh, S., Hwang, H., Kim, Y., & Park, D. (2009) · Archives of Dermatological Research · doi:10.1007/s00403-008-0924-4 · Cited by 20

Peptide OA-VI12 restrains melanogenesis in B16 cells and C57B/6 mouse ear skin via the miR-122-5p/Mitf/Tyr axis

Wang, J., Li, Y., Feng, C., Wang, H., Li, J., Liu, N., Fu, Z., Wang, Y., Wu, Y., Liu, Y., et al. (2023) · Amino Acids · doi:10.1007/s00726-023-03341-x · Cited by 19

Phytochemicals in the treatment of hyperpigmentation

Sivamani, R. K., & Clark, A. K. (2016) · Botanics Targets and Therapy · doi:10.2147/btat.s69113 · Cited by 19

Inhibitory Effect of Avenanthramides (Avn) on Tyrosinase Activity and Melanogenesis in α-MSH-Activated SK-MEL-2 Cells: In Vitro and In Silico Analysis

Park, J., Choi, H., Park, T., Lee, M., Lim, H., Yang, W., Hwang, C., Park, D., & Kim, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22157814 · Cited by 19

Thione Derivatives as Medicinally Important Compounds

Das, A., Ashraf, M. W., & Banik, B. K. (2021) · ChemistrySelect · doi:10.1002/slct.202102398 · Cited by 19

Development of actinobacterial resources for functional cosmetics

Dahal, R. H., Shim, D. S., & Kim, J. (2017) · Journal of Cosmetic Dermatology · doi:10.1111/jocd.12304 · Cited by 19

Neural Stem Cells and Its Derivatives as a New Material for Melanin Inhibition

Hwang, I.-S., & Hong, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms19010036 · Cited by 20

Synthesis of (S)-(+)-decursin and its analogues as potent inhibitors of melanin formation in B16 murine melanoma cells

Lee, K., Lee, J.-H., Boovanahalli, S. K., Choi, Y., Choo, S., Yoo, I., Kim, D. H., Yun, M. Y., Lee, G. W., & Song, G. (2010) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2010.09.006 · Cited by 18

Biotransformation of hydroquinone into α-arbutin by transglucosylation activity of a metagenomic amylosucrase

Agarwal, N., Rai, A. K., & Singh, S. P. (2021) · 3 Biotech · doi:10.1007/s13205-021-02909-2 · Cited by 18

Development of .ALPHA.-Arbutin: Production at Industrial Scale and Application for a Skin-Lightening Cosmetic Ingredient

Sugimoto, K., Nishimura, T., & Kuriki, T. (2007) · Trends in Glycoscience and Glycotechnology · doi:10.4052/tigg.19.235 · Cited by 18

Inhibitory effects of 6-(3-hydroxyphenyl)-2-naphthol on tyrosinase activity and melanin synthesis

Chung, S. W., Ha, Y. M., Kim, Y. J., Song, S., Lee, H., Suh, H., & Chung, H. Y. (2009) · Archives of Pharmacal Research · doi:10.1007/s12272-009-1235-9 · Cited by 18

Molecular design of potent, hydrophilic tyrosinase inhibitors based on the natural dihydrooxyresveratrol skeleton

Tanaka, Y., Suzuki, M. S., Kodachi, Y., & Nihei, K. (2018) · Carbohydrate Research · doi:10.1016/j.carres.2018.11.006 · Cited by 18

Inhibitory effect of ephedrannins A and B from roots of Ephedra sinica STAPF on melanogenesis

Kim, I., Yoon, S., Park, Y.-J., & Lee, H.-B. (2015) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2015.04.001 · Cited by 18

Structure–activity relationship of naphthaldehydethiosemicarbazones in melanogenesis inhibition

Pillaiyar, T., Eeda, V., LEE, K. ‐., Sharma, V. K., Roh, E., Kim, Y. S., & Jung, S. (2011) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2011.12.035 · Cited by 18

Multi-spectroscopic studies on the interaction between traditional Chinese herb, helicid with pepsin

Meti, M. D., Xu, Y. J., Xie, J., Chen, Y., Wu, Z., Liu, J., Han, Q., He, Z., Hu, Z., & Xu, H. Y. (2018) · Molecular Biology Reports · doi:10.1007/s11033-018-4306-5 · Cited by 18

Byelyankacin: A Novel Melanogenesis Inhibitor Produced by Enterobacter sp. B20

Takahashi, S., Iwai, H., Kosaka, K., Miyazaki, T., Osanai, Y., Arao, N., Tanaka, K. R., Nagai, K., & Nakagawa, A. (2007) · The Journal of Antibiotics · doi:10.1038/ja.2007.93 · Cited by 18

Effects of phenolic compounds isolated from Rabdosia japonica on B16‐F10 melanoma cells

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