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1,2,3,3a-Tetrahydro-3a-hydroxy-6-methyl-1-phenyl-4H-pyrrolo(2,3-b)quinolin-4-one

HCID 3476986
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Basic information

CAS
674289-55-5
Standard SMILES
Cc1ccc2c(c1)C(=O)C1(O)CCN(c3ccccc3)C1=N2
InChIKey
LZAXPYOBKSJSEX-UHFFFAOYSA-N
Molecular formula
C18H16N2O2
Average molar mass
292.3 g/mol
Monoisotopic mass
292.12117776

Overview

Blebbistatin is a pyrroloquinoline that is 1,2,3,3a-tetrahydro-H-pyrrolo[2,3-b]quinolin-4-one substituted by a hydroxy group at position 3a, a methyl group at position 6 and a phenyl group at position 1. It acts as an inhibitor of ATPase activity of non-muscle myosin II. It has a role as an inhibitor. It is a tertiary alpha-hydroxy ketone, a tertiary alcohol, a cyclic ketone and a pyrroloquinoline.

Names & identifiers

Preferred name
1,2,3,3a-Tetrahydro-3a-hydroxy-6-methyl-1-phenyl-4H-pyrrolo(2,3-b)quinolin-4-one
IUPAC
3a-hydroxy-6-methyl-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-one
English name
(+/-)-BLEBBISTATIN
Molecular formula
C18H16N2O2
Molecular weight
292.33

Names & synonyms

Blebbistatin674289-55-5(+-)-BlebbistatinCHEBI:7537920WC4J7CQ61,2,3,3a-Tetrahydro-3a-hydroxy-6-methyl-1-phenyl-4H-pyrrolo[2,3-b]quinolin-4-one1,2,3,3A-TETRAHYDRO-3A-HYDROXY-6-METHYL-1-PHENYL-4H-PYRROLO(2,3-B)QUINOLIN-4-ONERefChem:120622(+/-)-Blebbistatin3a-hydroxy-6-methyl-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-one3a-hydroxy-6-methyl-1-phenyl-1,2,3,3a-tetrahydro-4H-pyrrolo[2,3-b]quinolin-4-one( inverted exclamation markA)-Blebbistatin
Show more names
(±)Bebbistatin(R)-(+)-BLEBBISTATINBlebbistatin, 10 mM in DMSOE1249 (+/-)-Blebbi- Calbiochem(±)-Blebbistatin (DMSO Solution)Blebbistatin,Inhibitor,Myosin,inhibit(±)-Blebbistatin, inhibitor of myosin II(±)-Blebbistatin, inhibitor of myosin II
KBioGR_000194CHEMBL13283241-Phenyl-1,2,3,4-tetrahydro-4-hydroxypyrrolo(2.3-b)-7-methylquinolin-4-oneMFCD041137753a-hydroxy-6-methyl-1-phenyl-3,3a-dihydro-1H-pyrrolo[2,3-b]quinolin-4(2H)-oneSR-01000597498UNII-20WC4J7CQ6Blebbistain

Properties

Computed structural propertiesFilling in

XLogP
2.4
Topological polar surface area
52.9 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
1
Heavy atoms
22
Formal charge
0
Complexity
497

Physicochemical properties

Melting point
210 · 210-212°C
Boiling point
507.3 · 507.3±60.0 °C(Predicted)
Density
1.31 · 1.31±0.1 g/cm3(Predicted)
storage temp.
20 °C · −20°C
solubility
Chloroform (Slightly), Dichloromethane, DMSO, Ethyl Acetate, Methanol
form
Bright yellow solid.
pka
11.15 · 11.15±0.20(Predicted)
color
Yellow
InChI
InChI=1S/C18H16N2O2/c1-12-7-8-15-14(11-12)16(21)18(22)9-10-20(17(18)19-15)13-5-3-2-4-6-13/h2-8,11,22H,9-10H2,1H3
InChIKey
LZAXPYOBKSJSEX-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(C)C=C2)C(=O)C2(O)CCN(C3=CC=CC=C3)C=12
CAS DataBase Reference
674289 · 674289-55-5
FDA UNII
20 WC4J7CQ6 · 20WC4J7CQ6
UNSPSC Code
12352200 · 12352200
NACRES

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

wgk
WGK 2
risk_code
20/21/22-36/37/38
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xn
safety_code
26-36/37
Storage Class
11 - Combustible Solids
Hazard statements
H302-H315-H319-H335
Precautionary statements
P261-P305+P351+P338

Chemistry & industry

Applications · 3 items

Description(±)-Blebbistatin is a racemic mixture of (–)-blebbistatin and (+)-blebbistatin , the active and inactive forms, respectively. (–)-Blebbistatin is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (–)-Blebbistatin rapidly and reversibly inhibits Mg-ATPase activity and in vitro motility of non-muscle myosin IIA and IIB for several species (IC50s = 0.5-5 μM), while poorly inhibiting smooth muscle myosin (IC50 = 8 μM). Through these effects, (–)-blebbistatin blocks apoptosis-related bleb formation, directed cell migration, and cytokinesis in vertebrate cells. However, prolonged exposure to blue light (450-490 nm) results in degradation of blebbistatin to an inactive product via cytotoxic intermediates, which may be problematic for its use in fluorescent live cell imaging applications. (S)-nitro-Blebbistatin and (R)-nitro-blebbistatin are more stable forms of (–)-blebbistatin and (+)-blebbistatin, respectively. The addition of a nitro group stabilizes the molecules to circumvent their degradation by prolonged blue light exposure. (S)-nitro-Blebbistatin and (R)-nitro-blebbistatin have the same stereochemistry of the active and inactive enantiomers, respectively.

UsesBlebbistatin blocked myosin II-dependent cell processes. It blocks cell blebbing rapidly and reversibly. Also rapidly disrupted directed cell migration and cytokinesis in vertebrate cell. It blocks both blebbing and cytokinesis at 50-100μM. (±)-1-Phenyl-1,2,3,4-tetrahydro-4-hydroxypyrrolo[2,3-b]-7-methylquinolin-4-one Selective inhibitor of nonmuscle myosin II; inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. Rapidly and reversibly blocks cell blebbing, and disrupts directed cell migration and cytokinesis in vertebrate cells.

Uses(±)-Blebbistatin is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. It rapidly and reversibly inhibits Mg-ATPase activity and in vitro motility of non-muscle myosin IIA and IIB for several species (IC50 = 0.5-5.0 μM), while poorly inhibiting smooth muscle myosin (IC50 = 80 μM). Through these effects, blebbistatin blocks apoptosis-related bleb formation, directed cell migration and cytokinesis in vertebrate cells. Blebbistatin is inactivated by UV light, which may be particularly important in fluorescent cell imaging applications. Purified enantiomers of Blebbistatin are also available from Cayman (()-Blebbistatin - ).

Additional notes · 1 item

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Database identifiers

CAS
674289-55-5
PubChem CID
3476986
DTXSID
DTXSID501017342
ChEMBL
CHEMBL1328324
ChEBI
CHEBI:75379
UNII
20WC4J7CQ6
Nikkaji
J1.888.295G
77 · NA.77
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H335
Precautionary statements
261 · P261-P305+P351+P338
Hazard Codes
Xn
Risk Statements
20 · 20/21/22-36/37/38
Safety Statements
26 · 26-36/37
WGK Germany
2 · WGK 2
Storage Class
11 · 11 - Combustible Solids

DefinitionChEBI: A pyrroloquinoline that is 1,2,3,3a-tetrahydro-H-pyrrolo[2,3-b]quinolin-4-one substituted by a hydroxy group at position 3a, a methyl group at position 6 and a phenyl group at position 1. It acts as an inhibitor of ATPase ac ivity of non-muscle myosin II.