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ChemicalBook >> CAS DataBase List >>PAXILLINE

PAXILLINE

CAS No.
57186-25-1
Chemical Name:
PAXILLINE
Synonyms
PAXILINE;mycillin;PAXILLINE;Paxicillin;Paxilline solution;Paxilline in Methanol;fromPenicilliumpaxilli;PAXILLINE, PENICILLIUM PAXILLI;paxilline from penicillium paxilli;Paxilline, Ca2+-activated K+channel blocker
CBNumber:
CB2402640
Molecular Formula:
C27H33NO4
Molecular Weight:
435.56
MDL Number:
MFCD00083464
MOL File:
57186-25-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:24:56
Product description Number Pack Size Price
Paxilline powder, ≥98% (HPLC) P2928 5mg $480
Paxilline ≥98% 11345 1mg $50
Paxilline ≥98% 11345 5mg $134
Paxilline ≥98% 11345 10mg $242
Paxilline ≥98% 11345 1mg $45
More product size

PAXILLINE Properties

Flash point 2℃
storage temp. 2-8°C
solubility Soluble in DMSO, acetone or chloroform.
form powder
color faint yellow
Major Application cleaning products
cosmetics
food and beverages
personal care
InChIKey ACNHBCIZLNNLRS-UBGQALKQSA-N
SMILES N1C2=C(C=CC=C2)C2C[C@@]3([H])[C@](C)(C1=2)[C@@]1(C)CC[C@]2([H])O[C@H](C(O)(C)C)C(=O)C=C2[C@]1(O)CC3
FDA UNII 3T9U9Z96L7
UNSPSC Code 85151701

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
Signal word  Danger
Hazard statements  H301+H311+H331-H315-H318-H335
Precautionary statements  P261-P280-P301+P310-P302+P352+P312-P304+P340+P311-P305+P351+P338
Hazard Codes  T,Xn,F
Risk Statements  23/24/25-36/37/38-41-36-20/21/22-11
Safety Statements  26-36/37/39-45-36/37-16
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  DJ2830000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29419090
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
NFPA 704
0
4 0

PAXILLINE price More Price(55)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P2928 Paxilline powder, ≥98% (HPLC) 57186-25-1 5mg $480 2026-04-30 Buy
Cayman Chemical 11345 Paxilline ≥98% 57186-25-1 1mg $50 2026-04-30 Buy
Cayman Chemical 11345 Paxilline ≥98% 57186-25-1 5mg $134 2026-04-30 Buy
Cayman Chemical 11345 Paxilline ≥98% 57186-25-1 10mg $242 2026-04-30 Buy
Cayman Chemical 11345 Paxilline ≥98% 57186-25-1 1mg $45 2024-03-01 Buy
Product number Packaging Price Buy
P2928 5mg $480 Buy
11345 1mg $50 Buy
11345 5mg $134 Buy
11345 10mg $242 Buy
11345 1mg $45 Buy

PAXILLINE Chemical Properties,Uses,Production

Description

A complex alkaloid, paxilline occurs in the mycelium of the mold Penicillium paxilli. The structure has been confirmed by X-ray crystallography. The crystals are orthorhombic with space group P2 12 121 and a = 31.009, b = 11.522 and c = 7.70 A.

Description

Paxilline is an indole diterpene from fungi which potently and reversibly inhibits large conductance Ca2+-activated K+ (BKCa) channels, as shown in patch clamp (Ki = 1.9 nM) and whole smooth muscle cell studies (Ki = 35.7 nM). It also enhances the binding of charybdotoxin , a peptidyl neurotoxin, to BKCa channels. Paxilline is currently used to evaluate the role of BKCa channels in various cell processes and responses.

Chemical Properties

Powder

Uses

Potent blocker of high-conductance calcium-activated potassium (BKCa) channels

Uses

Paxilline is a tremorgenic mycotoxin isolated from species of Penicillium, Acremonium and Emericella. Paxilline selectively blocks high-conductance Ca2+-activated potassium channels and inhibits binding to the cerebellar inositol 1,4,5-triphosphate (InsP(3)) receptor.

Definition

ChEBI: Paxilline is an indole diterpene alkaloid with formula C27H33NO4 isolated from Penicillium paxilli. It is a potent inhibitor of large conductance Ca2(+)- and voltage-activated K(+) (BK)-type channels. It has a role as a mycotoxin, a Penicillium metabolite, an anticonvulsant, an Aspergillus metabolite, a potassium channel blocker, a genotoxin, a geroprotector and an EC 3.6.3.8 (Ca(2+)-transporting ATPase) inhibitor. It is an organic heterohexacyclic compound, a tertiary alcohol, a terpenoid indole alkaloid, an enone and a diterpene alkaloid.

Biological Activity

Potent blocker of high-conductance Ca 2+ -activated K + (BK Ca ) channels. Binds to the α -subunit of BK Ca (K i = 1.9 nM for block of currents in α -subunit-expressing oocytes) and enhances binding of charybdotoxin to BK Ca channels in vascular smooth muscle. Also inhibits sarco/endoplasmic reticulum Ca 2+ -ATPase (IC 50 = 5-50 μ M).

Enzyme inhibitor

This BKCa/KCa1.1) channel blocker (FW = 435.56 g/mol; CAS 57186-25-1; Solubility: 100 mM in DMSO), also named (2R,4bS,6aS,12bS,12cR,14aS)- 5,6,6a,7,12,12b,12c,13,14,14a-decahydro-4b-hydroxy-2-(1-hydroxy-1- methylethyl)-12b,12c-dimethyl-2H-pyrano[2'',3'': 5',6']benz[1',2':6,7]indeno [1,2-b]indol-3(4bH)-one, binds to the α-subunit of BKCa, exhibiting a Ki value of 1.9 nM in blocking currents in α-subunit-expressing oocytes and enhancing binding of to BKCa channels in vascular smooth muscle. (See Charybdotoxin) Paxilline also inhibits sarco/endoplasmic reticulum Ca2+-ATPase, IC50 = 5 - 50 μM.

storage

-20°C (desiccate)

References

Springer et ai., Tetrahedron Lett., 2531 (1975)

PAXILLINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 146)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32468 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39037 58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
+86-13119157289 18791163155@163.com China 3397 58
Aladdin Scientific
tp@aladdinsci.com United States 52923 58
Asperillum Ltm 15920419256 huangxishan13@foxmail.com China 142 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15838 69
Dalian Meilun Biotech Co., Ltd. 0411-62910999 13889544652 sales@meilune.com China 4764 58
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51395 80
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8447 60

View Lastest Price from PAXILLINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Paxilline pictures 2026-04-20 Paxilline
57186-25-1
$399.00 10g TargetMol Chemicals Inc.
  • Paxilline pictures
  • Paxilline
    57186-25-1
  • $399.00
  • TargetMol Chemicals Inc.
(2R)-5,6,6aα,7,12,12b,12c,13,14,14aβ-Decahydro-4bβ-hydroxy-2-(1-hydroxy-1-methylethyl)-12bβ,12cα-dimethyl-2H-1-benzopyrano[5',6':6,7]indeno[1,2-b]indol-3(4bH)-one 2h-1-benzopyrano(5’,6’:6,7)indeno(1,2-b)indol-3(4bh)-one,5,6,6a,7,12,12b,12c,1 4b-beta,6a-alpha,12b-beta,12c-alpha,14a-beta)-2-alph paxilline from penicillium paxilli PAXILINE Paxicillin (2R,4bS,6aS,12bS,12cR,14aS)-4b-Hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-2H-chromeno[5′,6′:6,7]indeno[1,2-b]indol-3(4bH)-one solution Paxilline solution PAXILLINE PAXILLINE, PENICILLIUM PAXILLI (2R,4BS,6AS,12BS,12CR,14AS)-5,6,6A,7,12,12B,12C,13,14,14A-DECAHYDRO-4B-HYDROXY-2-(1-HYDROXY-1-METHYLETHYL)-12B,12C-DIMETHYL-2H-PYRANO[2'',3'':5',6']BENZ[1',2':6,7]INDENO[1,2-B]INDOL-3(4BH)-ONE 14,14a-decahydro-4b-hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-( 2H-1-Benzopyrano[5',6':6,7]indeno[1,2-b]indol-3(4bH)-one, 5,6,6a,7,12,12b,12c,13,14,14a-decahydro-4b-hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-, (2R,4bS,6aS,12bS,12cR,14aS)- Paxilline,(2R,4bS,6aS,12bS,12cR,14aS)-5,6,6a,7,12,12b,12c,13,14,14a-Decahydro-4b-hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-2H-pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indol-3(4bH)-one 4b-Hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-2H-chromeno[5',6':6,7]indeno[1,2-b]indol-3(4bH)-one mycillin Paxilline in Methanol Paxilline, Ca2+-activated K+channel blocker fromPenicilliumpaxilli 57186-25-1 C27H33NO4 BioChemical Cell Biology Cell Signaling and Neuroscience Monovalent Ion Channels Potassium Channel Modulators Ion Channels Voltage-gated Ion Channels MoldVoltage-gated Ion Channels Cell Signaling and Neuroscience Monovalent Ion Channels Potassium Channel Modulators Toxins and Venoms Potassium channel antibiotic
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