2. Natural Products
  3. Plants
  4. Moraceae
  5. Morus alba Linn.

Morus alba Linn.

Synonyms: mulberry

Morus alba Linn. (30):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-17556
    Folinic acid 58-05-9 99.90%
    Folinic acid (Leucovorin) is a biological folic acid and is generally administered along with Methotrexate (MTX) (HY-14519) as a rescue agent to decrease MTX-induced toxicity.
    Folinic acid
  • HY-N0640
    Kuromanin chloride 7084-24-4 99.50%
    Kuromanin chloride (Chrysontemin) is derived from mulberry leaves and has the effect of increasing blood sugar concentration and maintaining lipid metabolism balance to reduce obesity. Kuromanin chloride can inhibit CD38 enzymatic activities.
    Kuromanin chloride
  • HY-14860
    1-Deoxynojirimycin 19130-96-2 ≥98.0%
    1-Deoxynojirimycin (Duvoglustat) is a potent and orally active α-glucosidase inhibitor. 1-Deoxynojirimycin suppresses postprandial blood glucose and is widely used for diabetes mellitus. 1-Deoxynojirimycin possesses antihyperglycemic, anti-obesity, and antiviral features.
    1-Deoxynojirimycin
  • HY-N0787
    Cryptochlorogenic acid 905-99-7 99.88%
    Cryptochlorogenic acid (4-Caffeoylquinic acid) is a naturally occurring phenolic acid compound with oral effectiveness, anti-inflammatory, antioxidant and anti-cardiac hypertrophy effects. Alleviating LPS (HY-D1056) and ISO (HY-B0468) by regulating proinflammatory factor expression, inhibiting NF-κB activity, promoting Nrf2 nuclear transfer, and regulating PI3Kα/Akt/ mTOR / HIF-1α signaling pathway Induced physiological stress response.
    Cryptochlorogenic acid
  • HY-122942
    Moracin M 56317-21-6 98.90%
    Moracin M is a phenolic component that can be isolated from Mori Cortex, is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity.
    Moracin M
  • HY-N3240
    Mulberrofuran C 77996-04-4
    Mulberrofuran C (compound 11) is an isoprene based flavonoid compound that can be extracted from the root bark of mulberry trees. Mulberrofuran C has protective effect on t-BHP induced oxidative stress with EC50 value of 1.02 μM. Mulberrofuran C has hepatoprotective and neuroprotective activities.
    Mulberrofuran C
  • HY-N5154
    Sanggenon W 2226467-12-3
    Sanggenon W is an isoprenyl flavonoid extracted from mulberry root bark.
    Sanggenon W
  • HY-N12721
    α-Glucosidase-IN-59
    α-Glucosidase-IN-59 (Compound 5b) is an inhibitor for α-glucosidase with IC50 of 1.16 μM.
    α-Glucosidase-IN-59
  • HY-N4247
    Kuwanon G 75629-19-5 99.52%
    Kuwanon G is a flavonoid isolated from Morus alba, acts as a bombesin receptor antagonist, with potential antimicrobial activity.
    Kuwanon G
  • HY-N0617
    Sanggenon C 80651-76-9 98.50%
    Sanggenon C, a flavonoid, exerts protective effects against cardiac hypertrophy and fibrosis via suppression of the calcineurin/NFAT2 pathway. Sanggenon C inhibits mitochondrial fission to induce apoptosis by blocking the ERK signaling pathway. Sanggenon C inhibits inducible nitric oxide synthase expression in RAW264.7 cells, and TNF-α-stimulated cell adhesion and VCAM-1 expression, by suppressing NF-κB activity. Sanggenon C possesses antioxidant, anti-inflammatory and antitumor activities.
    Sanggenon C
  • HY-N0618
    Sanggenon D 81422-93-7 99.76%
    Sanggenon D is a Diels-Alder-type adduct from Chinese crude agent root bark of mulberry ( Morus alba L.). Sanggenon D possesses antioxidant and inhibits Pancreatic lipase (PL) with the an IC50 of 0.77 μM.
    Sanggenon D
  • HY-N3239
    Mulberrofuran G 87085-00-5 99.84%
    Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM.
    Mulberrofuran G
  • HY-N2600
    Kuwanon H 76472-87-2 98.60%
    Kuwanon H is a flavonoid isolated from Morus alba, which acts as a potent non-peptide bombesin receptor antagonist. Kuwanon H selectively inhibits binding of gastrin releasing peptide CRP to GRP-preferring recepotr, with a Ki value of 290 nM in cells.
    Kuwanon H
  • HY-N3244
    Moracin O 123702-97-6 99.95%
    Moracin O is a 2-arylbenzofuran isolated from the Morus alba Linn. . Moracin O exhibits potent in vitro inhibitory activity against hypoxia-inducible factor (HIF-1). Moracin O reduces oxygen-glucose deprivation (OGD)-induced reactive oxygen species (ROS) production. Moracin O has neuroprotective and anti-inflammatory effects.
    Moracin O
  • HY-N0620
    Mulberroside C 102841-43-0 99.77%
    Mulberroside C is one of the main bioactive constituents in mulberry (Morus alba L.). Mulberroside C is a HCV replicon inhibitor. Antiviral activity.
    Mulberroside C
  • HY-N11531
    Kuwanon W 95518-95-9
    Kuwanon W is a natural product that can be isolated from the root bark of Morus lhou.
    Kuwanon W
  • HY-N2299
    Morusinol 62949-93-3 99.45%
    Morusinol is a flavonoid isolated from Morus alba root bark. Morusinol has an antiplatelet activity and  significantly inhibits arterial thrombosis in vivo.
    Morusinol
  • HY-N3516
    Oxyresveratrol 2-O-β-D-glucopyranoside 392274-22-5 99.08%
    Oxyresveratrol 2-O-β-D-glucopyranoside is a phenolic compound isolated from Morus nigra root and is an effective tyrosinase inhibitor with an IC50 of 29.75 μM.
    Oxyresveratrol 2-O-β-D-glucopyranoside
  • HY-N3668
    Cyclomorusin 62596-34-3
    Cyclomorusin (Cyclomorusin A; Cyclomulberrochromene) is a prenylflavonoid with antiplatelet activity. Cyclomorusin also inhibits markedly collagen-induced platelet aggregation.
    Cyclomorusin
  • HY-N0619A
    cis-Mulberroside A 166734-06-1
    cis-Mulberroside A (Mulberroside D) is the cis-isomer of Mulberroside A. Mulberroside A is one of the main bioactive constituent in mulberry (Morus alba L.). Mulberroside A decreases the expressions of TNF-α, IL-1β, and IL-6 and inhibits the activation of NALP3, caspase-1, and NF-κB and the phosphorylation of ERK, JNK, and p38, exhibiting anti-inflammatory and anti-apoptotic effects. Mulberroside A shows inhibitory activity against mushroom tyrosinase with an IC50 of 53.6 μM.
    cis-Mulberroside A